Chalmers et al. (2019) [ ]
cCBT computerized cognitive behavior therapy; DBT dialectical behavior therapy; HRV heart rate variability; MBSR mindfulness-based stress reduction; PosMT positive mental training; QoL quality of life; SFBT solution-focused brief therapy; SSRI selective serotonin reuptake inhibitor; TBI traumatic brain injury.
We used the PsycInfo database to map each intervention to its broader subject heading category and identified the theory or hypothesis associated with each that would lead to an improvement in stress-related outcomes. Although there was wide variability in the types of intervention trialed, most (22; 92%) utilized psychosocial interventions targeted at the individual level. These include social support [ 43 ], cognitive processes including mindfulness-based stress reduction, meditation and problem-solving therapy [ 28 , 31 , 44 , 47 ], rehabilitation or neuropsychological rehabilitation targeted at memory or leisure [ 29 , 40 ], a behavioral proactive coping intervention [ 30 ], physical activity programs [ 41 , 45 , 51 ], psychotherapy including both positive psychotherapy [ 42 , 54 ] and solution-focused brief therapy [ 55 ], creative arts therapy [ 37 ], cognitive behavioral therapy or positive mental training [ 48 , 52 ], multicomponent interventions consisting of home-based visits and mailed information, based on principles of psychoeducation [ 38 , 50 , 53 ] and training modules based on developing skills in either cognitive behavior therapy/cognitive reappraisal or heart rate variability biofeedback [ 36 , 39 ]. The remaining two studies assessed alternative medicine (aromatherapy massage and foot bath [ 46 ]), and pharmacological treatment (the selective serotonin reuptake inhibitor antidepressant sertraline [ 49 ]). There were no organizational-level interventions in the included studies.
Table 2 summarizes how stress or stress-relevant outcomes were measured in the included studies. Not all studies were designed to examine stress or resilience as a primary outcome, and as such the included outcomes were not necessarily primary outcomes. Studies were included into this scoping review only if the stress was specifically discussed in the results section of the study. This may include data from qualitative interviews or surveys, or within a subscale of another measure (e.g., QoL).
Characteristics of outcome measures used to assess interventions for stress measurement
Outcome type | Outcome measurement scale | Studies |
---|---|---|
Stress | 10-item Perceived Stress Scale (PSS-10) | Colledge et al. (2017) [ ] Ostwald et al. (2014) [ ] |
Depression Anxiety Stress Scales (DASS-21) | Cullen et al. (2018) [ ] | |
General Health Questionnaire (GHQ) | Friedland and McColl (1992) [ ] | |
Kessler Psychological Distress Scale (K10) | Jones et al. (2016) [ ] | |
Mental Fatigue Scale (MFS) | Johansson et al. (2012) [ ] | |
Social Readjustment Rating Scale (SRRS) | Lee et al. (2017) [ ] | |
Emotional Distress Scale (EDS) | Murray et al. (2005) [ ] | |
Coping | Utrecht Proactive Coping Competence scale (UPCC) | Tielemans et al. (2015) [ ] |
Coping Inventory for Stressful Situations | Visser et al. (2016) [ ] | |
Problem-solving | Social Problem-Solving Inventory-Revised (SPSIR) | Chalmers et al. (2019) [ ] Visser et al. (2016) [ ] |
Resilience | 10-item Connor Davidson Resilience Scale (CD-RISC) | Terrill et al. (2018) [ ] Perez-de la Cruz (2020) [ ] |
Brief Resilience Scale (BRS) | Love et al. (2020) [ ] | |
Depression/anxiety/mood | Center for Epidemiologic Studies Depression Scale (CES-D) | Chalmers et al. (2019) [ ] Visser et al. (2016) [ ] Love et al. (2020) [ ] |
Beck Depression Inventory (BDI) | Colledge et al. (2017) [ ] Nour et al. (2002) [ ] Simblett et al. (2017) [ ] | |
Beck Anxiety Inventory(BAI) | Simblett et al. (2017) [ ] | |
Hospital Anxiety and Depression Scale (HADS) | Chalmers et al. (2019) [ ] Stubberud et al. (2019) [ ] Tielemans et al. (2015) [ ] Wichowicz et al. (2017) [ ] | |
Comprehensive Psychopathological Rating Scale (CPRS) | Johansson et al. (2012) [ ] | |
Multiple Affective Adjective Checklist (MAACL) | Lee et al. (2017) [ ] | |
Montgomery–Åsberg Depression Rating Scale (MADRS) | Murray et al. (2005) [ ] | |
Presence of emotionalism (increased tearfulness and pathologic crying was recorded as a dichotomous variable) | Murray et al. (2005) [ ] | |
Geriatric Depression Scale (GDS) | Ostwald et al. (2014) [ ] | |
PROMIS-Depression Short Form 8b | Terrill et al. (2018) [ ] | |
State-Trait Anxiety Inventory (STAI-Y) | Love et al. (2020) [ ] | |
Quality of life | Stroke Specific Quality of Life Scale (SS-QOL) | Chalmers et al. (2019) [ ] Tielemans et al. (2015) [ ] Visser et al. (2016) [ ] |
Global subjective rating of change in quality of life (QoL) was measured according to a validated visual analog scale | Murray et al. (2005) [ ] | |
Sickness Impact Profile | Nour et al. (2002) [ ] Friedland and McColl (1992) [ ] | |
Older People’s Quality of Life Questionnaire (OPQOL) | Terrill et al. (2018) [ ] | |
Short From 36 Health Survey (SF-36) | Perez-de la Cruz (2020) [ ] | |
EuroQol EQ-5D-5L | Visser et al. (2016) [ ] | |
Life satisfaction | Satisfaction with Life Scale (SWLS) | Colledge et al. (2017) [ ] |
Authentic Happiness Inventory (AHI) | Cullen et al. (2018) [ ] | |
Leisure Satisfaction Scale | Nour et al. (2002) [ ] | |
Likert scales: current life satisfaction, and the difference from prestroke life satisfaction | Cullen et al. (2018) [ ] | |
Qualitative analysis | Open-ended descriptive survey | Chalmers et al. (2019) [ ] |
Semi-structured interviews | Chouliara and Lincoln (2016) [ ] Mavaddat et al. (2017) [ ] Baumann et al. (2013) [ ] |
Several different psychometric scales were used to assess stress or related constructs; however, we found no studies assessing stress biomarkers. In our search strategy, we included terms for coping and resilience, resulting in the inclusion of studies that measured stress, and resilience, coping, problem-solving, stress-related disorders (including anxiety, depression, and PTSD), life satisfaction, and QoL measures, where stress was reported as a subcomponent of the measure. Of the 14 studies which included a psychometric measurement of stress, coping, or resilience, 8 reported using a stress-specific outcome measure [ 41–46 , 49 , 50 ], with others recording stress-related constructs via a coping scale [ 30 , 31 ], problem-solving scale [ 28 , 31 ], or resilience scale [ 47 , 51 , 54 ].
Most studies measured stress-related disorders via a scale for symptoms of depression, anxiety, or mood ( n = 16) [ 28–31 , 36 , 39 , 41 , 44 , 46 , 47 , 49 , 50 , 52–55 ]. The Center for Epidemiologic Studies Depression Scale (CES-D) [ 28 , 31 , 47 ], Beck Depression Inventory (BDI) [ 29 , 41 , 52 ], and the Hospital Anxiety and Depression Scale (HADS) [ 28 , 30 , 36 , 39 , 53 , 55 ] were the most commonly used measures.
Ten studies assessed QoL and/or life satisfaction [ 28–31 , 41–43 , 49 , 51 , 54 ]; some studies reported a stress measure as a subscale of this. For example, Friedland and McColl [ 43 ] used the General Health Questionnaire (GHQ) and the Sickness Impact Profile (SIP) to measure “psychosocial adjustment”. As mentioned above three qualitative thematic analysis studies [ 37 , 40 , 48 ] were included which did not measure stress outcomes but which highlighted stress as an emerging theme. For example, Baumann et al. [ 37 ], a descriptive study of an art therapy program aiming to reduce distress during rehabilitation, did not explicitly measure stress but described individual participants’ experiences of distress associated with stroke.
For each intervention, we assessed the effectiveness in terms of both reduction in stress or related construct, and reduction in stress-related mental health disorders (anxiety, depression, or PTSD); implementation measures including barriers and limitations, feasibility and acceptability, and any cost analysis or cost-effectiveness, were reported. Collectively, these features are likely to inform the further development of an intervention for eventual use in practice ( Table 3 ).
Measures of effectiveness, acceptability, feasibility, and cost-effectiveness
Study | Stress reduction | Reduction in anxiety or mood disorder | Barriers and limitations | Feasibility and acceptability | Cost-effectiveness |
---|---|---|---|---|---|
Bannon et al. (2020) [ ] | Increased scores on resiliency variables, including self-efficacy, mindfulness, and perceived coping in Recovering Together training dyads, but not control dyads from baseline to post-test. | Participation in Recovering Together was associated with baseline to post-test decrease in symptoms of depression, anxiety, and PTS in stroke survivors and caregivers. | Small feasibility trial Patients discharged before they could be approached Low internal consistency on measures with reversed scored items for patients at baseline | Clinical staff not invested in project Low recruitment Treatment satisfaction was high Adherence and acceptability of procedures was high | NR |
Baumann et al. (2013) [ ] | Weekly art sessions during rehabilitation. Participants reported that the sessions offered a source of relaxation, tranquility or calmness(qualitative analysis). | NR | No long-term follow-up (1 week after final session) Small sample size ( = 18) | All but one patient indicated a wish to continue arts activities in the future | NR |
Bragstad et al. (2020) [ ] | No between-group differences in psychosocial wellbeing at 12 months poststroke. | No statistically significant between-group difference in depression, sense of coherence, or health-related QoL at 12 months. | The intervention was designed both to be delivered uniformly and to be individualized. The competing aims may have compromised session delivery Sample may not be representative; informed consent was difficult to obtain in the stroke unit | Composite adherence score showed that 117 (80.1%) of the intervention trajectories satisfied the criteria for high-fidelity intervention adherence Participants reported finding the intervention helpful | NR |
Chalmers et al. (2019) [ ] | Problem-solving therapy did not produce a significant change in overall problem-solving (SPISR; proxy measure for emotional distress). | Slight reduction after therapy on the CES-D and no reduction on the HADS-A. | No randomization Use of waitlist control group No controlling for confounding Problems with recruitment Small sample size ( = 28) | Participants generally reported that each therapy session was helpful and enjoyable | NR |
Chang et al. (2020) [ ] | Average HR decreased compared with baseline in the HRVBF, but no significant difference between groups. | HADS score significantly decreased in the HRVBF group at 1 and 3 months but not in the control group. | Small sample size Short follow-up time Did not log self-practice during follow-up | 5/40 patients dropped out after randomization Study reported that the intervention was feasible, but it was not clear on what basis this was reported | NR |
Chouliara and Lincoln (2016) [ ] | Memory rehabilitation led to perceived benefits in participants’ ability to effectively manage stress (qualitative analysis). | NR | Small sample size ( = 20) Qualitative analysis did not directly assess some aspects Separate results not reported for stroke survivors only | NR | NR |
Colledge et al. (2017) [ ] | No effect of exercise training on perceived stress. | Descriptive reduction in depressive symptoms at follow-up. | Small sample size ( = 32) Exploratory trial (descriptive analysis only) Selection bias No nonintervention control group | NR | NR |
Cullen et al. (2018) [ ] | Mean difference of −5.8 points on the DASS-21 Stress scale (intervention vs. controls) at week 20 after positive psychology intervention. | Mean difference of −9.6 points on the DASS-21 Anxiety scale (intervention vs. controls) at week 20 after positive psychology intervention. | Small sample size ( = 37) Exploratory trial Not designed or powered for efficacy | 63% retention (15 completers) Authors considered intervention feasible to deliver and acceptable to participants | NR |
Friedland and McColl (1992) [ ] | No differences between social support intervention and control groups on psychosocial variables including the GHQ. | NR | Relatively high attrition rate Timing of intervention | NR | NR |
Johansson et al. (2012) [ ] | Statistically significant reduction in reported mental fatigue, including reduction in sensitivity to stress item, following MBSR compared with baseline and controls. | Significantly decreased scores for depression and anxiety on the CPRS after 8 weeks of MBSR. | Small sample size ( = 29) Some participants who discontinued found the program time consuming, or difficult to travel to attend appointments | NR | NR |
Jones et al. (2016) [ ] | A statistically significant reduction in psychological distress (K10 scale) of 2.76 points immediately after the myMoves program ( = .001). | NR | Small sample size ( = 24) Contact with study participants occurred outside of the intervention program Mixed population (stroke and TBI) | Participants completed an average of 5.6/6 sessions Participants reported a high level of overall satisfaction with the program (95.7%) The program required little clinician contact time, with an average of 32.8 min per participant over 8 weeks | NR |
Lee et al. (2017) [ ] | Statistically significant reduction in the social readjustment rating scale (means not reported). | NR | Small sample size ( = 14) Poor reporting of study methodology and results | NR | NR |
Love et al. (2020) [ ] | Small, but nonsignificant, postmeditation increase in resilience observed. | NR | Small sample size ( = 35) No control group Selection bias Sampling in single stroke clinic Exclusion of participants lost to follow-up | NR | NR |
Mavaddat et al. (2017) [ ] | In qualitative interviews, stroke survivors reported benefits of the positive mental training program in handling stress, improved mood, and coping ability. | Four stroke survivors had improved scores on PANAS; two stroke survivors had improved scores, and one stroke survivor had a worse score on the HADS. | Small sample size ( = 10) Self-selected sample Not all participants completed the full 12-week program | 7/10 stroke survivors reported positive benefits from listening and would recommend to others Participants with moderate aphasia found it difficult to concentrate and did not persist with the study | £38 for access to the full audio program (in 2013 GBP). |
Murray et al. (2005) [ ] | No statistically significant effect of sertraline treatment on EDS score, however there was a reduction from baseline in both groups regardless of treatment. Some improvement in QoL and emotionalism. | The MADRS score decreased substantially in both treatment groups, with no significant differences between them at 6 and 26 weeks. | High discontinuation rate (39% in the treatment and 49% in the placebo group) Selection of patients with minor depression only | NR | NR |
Nour et al. (2002) [ ] | At post-test, the experimental group (leisure rehabilitation) obtained statistically significantly better scores for total, psychological, and physical QoL, although effect sizes were small. | No statistically significant difference between groups for depression (BDI). | Small sample size Extra time (on average 20 min per session) provided to intervention group Some participants did not complete the program | Participants reported satisfaction with leisure activities following the intervention | NR |
Ostwald et al. (2014) [ ] | No effect of mailed or home-based psychoeducational intervention on stress as measured by the PSS-10. | No effect of mailed or home-based psychoeducational intervention on depression scores (GDS). | Sample size not large enough for subgroup analyses The sample is not representative—included only those over 50 years of age who were being discharged home with a spouse Analysis of multiple outcomes in this study possibly increased the type I error rate. | 84% of the dyads completed the study 12-month follow-up. Dyads that did not complete the study were older, had higher caregiver support scores and spent more days in inpatient rehabilitation than those who finished the study | Number, length, and content of each contact was tracked, allowing for analysis of costs. An average of two home visits a month during the initial 6 months at home postdischarge from inpatient rehabilitation could be delivered at a mean cost of $2,500 per dyad. |
Perez-de la Cruz (2020) [ ] | In the experimental group, significant differences from baseline were found in the resilience variables ( < .001) and these improvements were maintained 1 month after completing the treatment program. | NR | Small sample size ( = 41) Short follow-up (1 month) | All the participants completed all the sessions and complied with the proposed program | NR |
Simblett et al. (2017) [ ] | All groups demonstrated a decrease in symptoms of distress, measured via the BDI and BAI, and the NEADL across time associated with computerized CBT and computerized cognitive remediation therapy. | Trend toward reduced depression scores on the BDI for computerized CBT and computerized cognitive remediation therapy. Smaller trend for anxiety symptoms. | Small sample size ( = 28) Feasibility and acceptability were the primary outcomes for this study, not efficacy No blinding to intervention of outcome assessors | Feasibility and acceptability were the primary outcomes for this study. Recruitment rate for the intervention ran below the expected rate Broadly feasible, although some aspects required more flexibility Majority suggested intervention was useful, relevant and easy to use | Not explicitly measured. However, the idea of small groups was primarily introduced as a means of improving the feasibility of delivery by reducing costs associated with providing psychological therapy. |
Stubberud et al. (2019) [ ] | No change in self-efficacy after training in metacognitive strategies for improving attention, problem-solving, fatigue management, adaptive coping responses, and the use of CBT techniques as measured using the GSE scale. | Decrease in overall score on the HADS, driven by a change in the anxiety subscale. No change in the depression subscale. | Small sample size ( = 8, of which 5 are stroke survivors) Results not presented separately for stroke and TBI survivors Self-reported outcomes only No control group | All subjects completed the interventions | NR |
Terrill et al. (2018) [ ] | Study not designed to measure effect of intervention—the data collected in this study were used to identify feasibility of a positive psychology app. 8/10 dyads still used positive psychology in their everyday lives at follow-up. Measured CD-RISC, but results not reported. | Measured PROMIS-Depression Short Form 8b, but results not reported. | Small sample size; 11 stroke survivor/carer dyads. One dyad discontinued, final 10 dyads | Participants reported satisfaction with the intervention Stroke survivors were fatigued by training session One of the dyads dropped out of the study Remaining dyads engaged in a mean of 4.08 individual and 3.62 couple activities per week | Not explicitly reported; referenced a Cochrane review stating that use of apps to administer self-management programs was cost-effective. |
Tielemans et al. (2015) [ ] | No effect of self-management intervention compared with an education intervention in coping skills on the UPCC scale. | Trend favoring the self-management intervention on the HADS. | Study did not include more severely affected stroke survivors Self-assessment used to assess outcomes Outcome measures too generic to detect changes Study too small to detect outcome differences in partners ( = 57 partners) Sample selected by hospital staff Usual care was not controlled | Of 58 patients assigned to the self-management intervention, 56 started the intervention and 46 attended at least three quarters of the intervention sessions | NR |
Visser et al. (2016) [ ] | Improvement in coping strategy as measured by the Coping Inventory for Stressful Situations between groups (problem-solving therapy vs. control). | Depression score did not differ significantly between the groups over time (CES-D). | No active control groups Intervention was investigated within outpatient rehabilitation and may not be generalizable to other settings Sample reported a relatively high utility score compared with other stroke populations | The low dropout rate and positive feedback suggest that an open group design is feasible and effective in outpatient stroke rehabilitation | NR |
Wichowicz et al. (2017) [ ] | Increased self-efficacy and constructive attitudes in the SFBT group compared with controls (Mini-Mental Adjustment to Cancer and Self-efficacy Scale). | Reduced anxiety and depression scores in the SFBT group compared with controls (HADS). | 62 completers (100 randomized) Participants relatively fit and may not be representative 35 withdrawals from study Lengthy procedure Lack of complete randomization | Potential SFBT participants who refused to participate may have found the procedure of psychotherapy too lengthy | NR |
BAI Beck Anxiety Inventory; BDI Beck Depression Inventory; CD-RISC 10-item Connor Davidson Resilience Scale; CES-D Center for Epidemiologic Studies Depression Scale; CPRS Comprehensive Psychopathological Rating scale; DASS-21 Depression Anxiety Stress Scales; EDS Emotional Distress Scale; GBP British pounds; GDS Geriatric Depression Scale; GHQ General Health Questionnaire; GSE General Self-Efficacy; HADS Hospital Anxiety and Depression Scale; HR heart rate; HRVBF heart rate variability biofeedback; MADRS Montgomery–Åsberg Depression Rating Scale; MBSR mindfulness-based stress reduction; NEADL Nottingham Extended Activities of Daily Living; NR not reported; PANAS Positive and Negative Affect Schedule; PROMIS Patient-Reported Outcomes Measurement Information System; PSS-10 Perceived Stress Scale; PTS post-traumatic stress; QoL quality of life; SFBT solution-focused brief therapy; SPISR Social Problem-Solving Inventory-revised; TBI traumatic brain injury; UPCC Utrecht Proactive Coping Competence.
In order to address our research question “to identify which interventions are potentially efficacious for reducing stress or increasing resilience and coping” we compiled a descriptive overview of the reported effectiveness of the intervention in each study. Positive effects on stress, resilience, coping, or psychological QoL/life satisfaction were reported in 13 of the 24 included studies [ 29 , 31 , 36 , 37 , 40 , 42 , 44–46 , 48 , 51 , 52 , 55 ]. Baumann et al. [ 37 ] and Chouliara and Lincoln [ 40 ] reported qualitative reductions in stress associated with an inpatient art program and memory rehabilitation, respectively. The other studies reported a quantitative improvement in stress-related outcomes associated with a number of intervention types: skills-based training based on principles of cognitive behavior therapy [ 36 ], positive psychology [ 42 , 48 ], mindfulness-based stress reduction [ 44 ], physical activity program [ 45 ], aromatherapy massage, and footbath [ 46 ], leisure rehabilitation [ 29 ], aquatic therapy [ 51 ], computerized cognitive behavior therapy or cognitive remediation [ 52 ], problem-solving therapy [ 31 ], and solution-focused brief therapy [ 55 ]. Whilst this represents many included studies (54%), most of these had relatively small sample sizes, ranging from 14 to 166, with 10/13 studies recruiting fewer than 30 stroke survivors. Most of these were reported as exploratory, quasi-experimental, or feasibility studies, and reported other methodological concerns including lack of active control group and significant dropout rates. Some of these results were also not numerically reported or reported as a qualitative perceived reduction only.
The impact of the interventions on longer-term stress-related problems, primarily symptoms of depression or anxiety, were considered in 75% (18/24) included studies. Of these, seven reported a quantitative decrease in these symptoms [ 36 , 39 , 42 , 44 , 47 , 53 , 55 ].
In addition to effectiveness results, we also collated implementation outcomes reported across studies, primarily acceptability and feasibility, in order to assess whether the potential long-term sustainability of intervention had been considered in the included studies. Where studies included an explicit measure of feasibility or acceptability from participants, feedback was generally positive [ 28 , 29 , 31 , 36–39 , 42 , 45 , 46 , 48 , 50–52 , 54 ]. Several studies reported low dropout rates and high adherence to the intervention strategy ( n = 8) [ 31 , 36 , 38 , 45 , 50 , 51 , 53 , 54 ]. Broadly, this suggests a willingness to participate in these intervention studies. However, several studies did report problems with recruitment or other barriers to participation, including potential refusal to participate based on the time commitments or participation burden required for some interventions ( n = 8) [ 30 , 36 , 42–44 , 50 , 54 , 55 ]. Further, some interventions reported differential dropout rates for different groups of participants, particularly those with aphasia ( n = 2) [ 30 , 48 ].
We also investigated whether studies reported some measure of cost or cost-effectiveness analysis. This is also an important consideration for upscaling and eventually implementing a novel intervention in practice. Only four of the included studies referred to or measured the costs of the intervention. Mavaddat et al. [ 48 ] and Ostwald et al. [ 50 ] both reported the costs of providing the intervention per participant. In Terrill et al. [ 54 ] and Simblett et al. [ 52 ], although costs were not explicitly measured, both reported that the intervention was expected to be cost-effective based on its features. The cost-effectiveness of any intervention was not reported.
We used the Cochrane Risk of Bias tool to assess intervention studies, and the MMAT to assess mixed-method and qualitative studies ( Supplementary File 4 ). The included quantitative studies ( n = 21) [ 28–31 , 36 , 38 , 39 , 41–47 , 49–55 ] had methodological limitations, including unclear recruitment techniques, small sample sizes, high attrition rates, failure to control for important confounders, use of nonvalidated measures and inconsistent reporting. Studies scored most strongly (low risk of bias) on sequence generation (12/21), allocation concealment (11/21), incomplete outcome data (18/21), and selective outcome reporting (16/21). The categories where studies overall were weaker (associated with a high or unclear risk of bias) included blinding of participants and personnel (16/21), blinding of outcome assessors (14/21), and other sources of bias (20/21). Quality scoring of the qualitative or mixed-methods papers ( n = 3) [ 37 , 40 , 48 ] suggested that these papers had a moderate risk of bias. Studies were not excluded based on quality. The assessment of quality for each of the included studies is presented in Supplementary Appendix .
This scoping review is the first to map the breadth of research that has been conducted around stress interventions for stroke survivors. Here, we have mapped the types and effectiveness of the trialed interventions, as well as the outcome measures used to assess stress or related constructs. We also considered aspects of implementation reported in the studies, including patient acceptability, feasibility, limitations, and cost-effectiveness. We identified a total of 24 studies that recruited mixed populations of stroke survivors in terms of susceptibility to stress-related outcomes and time poststroke and identified a variety of primarily psychosocial interventions delivered to individuals to directly address stress management or promote related constructs such as resilience, problem-solving, or coping. Although all studies reported the effect of the intervention on stress or stress-related outcome measures, a correlation to recovery outcomes was not consistently addressed or investigated across studies. We also identified significant methodological issues associated with most studies, and a tendency for studies to be at an early or feasibility stage. Furthermore, even though the majority of included studies appeared to be feasibility or exploratory trials, our search did not identify any larger subsequent or follow-up studies to this early work. Overall, despite the trend toward positive outcomes, the limitations of the included studies made it difficult to conclusively identify the most effective interventions. Despite these shortcomings, we found that the number of relevant publications increased over time, suggesting that stress and stress management are progressively being considered important for stroke survivors.
Psychological distress is commonly reported following stroke and is associated with a number of significant cognitive and psychological problems, but based on this review, the evidence base for psychotherapeutic interventions is small and equivocal. Any recommendation for an intervention designed to manage excessive stress, with the ultimate aim of preventing stress-related disorders and improving recovery, should be evidence based in order to justify the allocation of resources, and in order to reduce harms from potentially ineffective interventions. Although there is emerging evidence for targeting stress for the prevention of some disorders such as CVD, at present the relevance of intervening on stress in stroke populations remains unclear [ 57 , 58 ]. Broadly, the population with the greatest benefit:risk ratio is not defined, the potential range of interventions remains broad, and there is no agreement on the best outcome measures to use for stress. The studies included here also tended to emphasize treatment rather than prevention of emotional distress. This is in agreement with two recent systematic reviews of dyadic interventions for caregivers and stroke survivors, which focused on interventions to reduce stress in caregivers. The results of these studies highlighted substantial limitations of interventions for carers and stroke survivors including weighting toward treating rather than preventing stress, and a lack of customizable interventions which would allow tailoring to account for the heterogeneity of stroke survivors’ needs [ 59 , 60 ].
A wide variety of interventions were trialed in the included studies, which were predominantly small in scale and based on very localized or intensive solutions generally run for an 8–12-week period. Often considerations on how such an intervention might scale up to the broader population were not included/made. Several studies reported poor adherence and/or recruitment due to the burden of participation. Stress management interventions that require large amounts of time and travel may lead to adherence problems in stroke survivors and should be an important consideration in the development of any intervention. Unlike pharmaceuticals, funding mechanisms for integrating new psychosocial interventions into health systems are less clear. Further, funding for sufficiently large effectiveness trials and eventual reimbursement should also be considered. These factors were rarely considered in the included studies. Adequate resourcing, and considering the burden of participation for stroke survivors and health systems, are important considerations in the design of any preventive intervention. This is likely to be magnified for an issue such as stress management, which will require significant adherence to achieve its goals.
In order to address issues around implementation, scalability, and cost-effectiveness, it may be worth considering interventions that have been trialed in other populations that may be likely associated with smaller participant burden, lower costs, and high effectiveness. For example, mobile technologies and mHealth interventions might be a low-cost, simple method of delivering modular, customized mental health support to mitigate stress in stroke survivors. Mobile interventions based on cognitive training approaches have been used successfully for stress-related cognitive problems such as memory impairment [ 61 ]. However, to date, there is very little regulation of these interventions and systematic research on the potential benefits of mHealth interventions for stress management is not currently available.
The relevant population for targeting stress management to prevent the stress-related sequelae of stroke also remains unclear. Prevention of stress after stroke could be either universal (i.e., offered to all individuals poststroke), or targeted to a higher risk population of stroke survivors identified as having elevated levels of stress prior to the stroke, or those most at risk of developing adverse stress-related outcomes. The studies included in this review were mixed; some included a broader population of stroke survivors (21/24), whilst others included only those at higher risk of stress and related sequelae, such as emotional distress or symptoms of depression (3/24). It is also unclear at which phase of stroke recovery is best to intervene. Although most of the included studies were conducted during the chronic phase of stroke recovery (i.e., >6 months poststroke), at present it remains unknown as to when might be the optimum time to manage stress throughout the recovery trajectory. Whilst the relative risk of negative health outcomes due to stress may be small compared with other risk factors, a recent review highlighted the importance of tackling stress in people with high baseline cardiovascular risk, such as stroke survivors, because this translates into a larger difference in absolute risk [ 62 ]. In order to determine when and in which population stress management might be most clinically and cost-effective, additional studies are required which monitor stress and related sequelae over time.
Additionally, several studies excluded people with a progressive neurological disorder, cognitive dysfunction, or aphasia. Studies typically justified this approach by stating that collecting and reliably interpreting data from these patients can present significant challenges. However, a high proportion of stroke patients have cognitive or speech, and language impairments, and if studies of interventions aiming to reduce psychological distress among stroke patients fail to involve such patients, the findings may not be representative of the wider stroke population [ 37 ]. Therefore, a number of these studies with specific inclusion/exclusion criteria may not be generalizable to the broader population with stroke and have limited external validity.
There was a lack of consistency in measuring stress between studies. Significant uncertainty in the field of stress research more broadly lies in the use of standardized techniques or tools to measure the level of stress. Whilst stress has been linked to an increased risk of secondary stroke, CVD, and psychopathology in stroke survivors, and has a negative impact on the trajectory of recovery from stroke, the best approach to measure stress in research and clinical settings remains unclear [ 63 , 64 ]. Compared with other known behavioral risk factors for chronic diseases, such as smoking, nutrition, and physical activity, psychosocial constructs such as stress are difficult to define objectively [ 65 ]. The response to stress can be measured using self-report, or a physiological measurement. A number of scales have been developed for the measurement of stress. The Perceived Stress Scale (PSS-10) [ 66 ], Symptom Checklist 90 (SCL-90) questionnaire [ 67 ], and the Depression Anxiety Stress Scales (DASS-21) [ 68 ] tend to be the most widely used validated tools found in the literature for the subjective assessment of stress. In this review, we found considerable variation across studies in terms of self-reported approaches for measuring stress. Several studies did not use any stress measurement tool, instead of reporting subscale results of a QoL scale or similar to infer emotional distress, qualitative results, or used an unstandardized tool, making it difficult to compare study results. Related constructs such as resilience also appeared infrequently in our search, with only three studies reporting the results of an intervention on a resilience scale.
Similarly, no studies reported changes in any biomarkers for stress. There are numerous biological pathways linking stress to disease outcomes, and as a result, a number of physiological stress measures or biomarkers are commonly used in stress research, primarily based on stress-related changes in neuroendocrine signaling [ 69 ]. One of the major alternatives to the psychometric assessment of stress is to assess levels of stress hormones, in blood or saliva [ 7 ]. A number of studies have considered a measurement of blood cortisol levels; however, these measures also suffer from serious limitations in terms of their accuracy because stress is not the only factor that evokes changes in the levels of these hormones [ 7 , 63 ]. Stress hormones measured within the saliva and blood can change quickly in their concentration and fluctuate significantly over time [ 70 ]. These issues mean that single-time point analyses using blood or saliva may be noninformative. Of course, it is possible to collect multiple samples across time, but the practical considerations and participant burden mean this is typically not feasible. One recent study has used an objective measure of the stress level in the form of hair cortisol, to associate stroke outcome with stress [ 71 ]. The hair sample for the determination of cortisol level instead of blood, saliva, or urine offers several advantages in stroke–stress research. Firstly, its analysis can provide an accurate assessment of the long-term integrated level of cortisol over the course of the months. Secondly, its measurement is not affected by acute stress variables and is not subject to diurnal variation, and finally, baseline hair samples obtained within the week after stroke provides information about stress and cortisol level prior to the stroke incident. The relatively stable and noninvasive nature of hair cortisol as a stress biomarker may make this an ideal marker in future studies of stress poststroke.
Finally, it has not yet been shown that a change on a subjective stress scale is a proxy for patient-relevant outcomes, such as prevention of anxiety or depression. Based on the included studies, there is only limited evidence to suggest that the included interventions to manage stress and related constructs will translate into a reduction in stress-related disorders in stroke survivors. In the included studies, only 7 of the 18 that considered symptoms of stress-related disorders reported a decrease in symptoms associated with the intervention. This may not be unexpected, since these programs were designed to address stress management and not treat existing symptoms of anxiety or depression. Whilst improved stress management is likely to be an important precursor to effective prevention of depression or anxiety, it remains unclear where best to target these efforts. In future studies, it will be important to establish not only consistent and relevant measures of stress, but also the link between an improvement in stress management or stress levels and reductions in the risk of known stress-associated disorders such as depression, anxiety, CVD, and mild cognitive impairment. Further, studies should examine longitudinally the impact of early compared with late stress mitigation, to examine whether stroke survivors who receive these preventive measures at varying time periods in recovery are less likely to develop stress-related problems.
There are a number of potential limitations to this review. While we conducted a comprehensive search using key databases and hand searching, it is possible that the review may have missed some relevant studies. We also included only papers in English and did not conduct a search of the gray literature. There may be evidence of program impacts in the evaluation and other technical reports, not available here.
The successful management of chronic stress in stroke survivors is likely to improve psychological and cognitive recovery outcomes and improve rehabilitation contacts. However, most intervention studies we identified were small, primarily consisting of feasibility studies to inform larger trials. There was a trend toward a positive effect of stress management interventions in stroke survivors, in terms of reduction in perceived stress levels, and a smaller trend toward a reduction in symptoms of anxiety and depression associated with improved stress management. It is unclear at this stage which population would benefit most, and which intervention could be recommended based on effectiveness and implementation outcomes. Additionally, it is still unclear how best to measure and monitor stress in stroke survivors. In order for the field to address the gaps and inconsistencies identified here, we must be able to effectively assess stress levels in individuals over time.
Overall, despite the heterogeneity of the studies covered in this review, there was a clear trend toward positive outcomes, and the number of studies conducted is increasing over time. As a field, this area is gaining attention, and future well-designed and properly powered studies will provide important answers to the questions raised in this review. Given that an increasing number of studies have identified that stress represents an unmet need for stroke survivors and is an important contributor to increased risk of poor recovery outcomes, addressing stress provides an opportunity to improve long-term outcomes for stroke survivors.
Kaac002_suppl_supplementary_file_1, kaac002_suppl_supplementary_file_2, kaac002_suppl_supplementary_file_3, kaac002_suppl_supplementary_file_4, contributor information.
Madeleine Hinwood, School of Medicine and Public Health, The University of Newcastle, Callaghan, NSW, Australia. Hunter Medical Research Institute, New Lambton Heights, NSW, Australia.
Marina Ilicic, Hunter Medical Research Institute, New Lambton Heights, NSW, Australia. School of Biomedical Sciences and Pharmacy, The University of Newcastle, Callaghan, NSW, Australia. Priority Research Centre for Stroke and Brain Injury, The University of Newcastle, Callaghan, NSW, Australia.
Prajwal Gyawali, School of Health and Wellbeing, Faculty of Health, Engineering and Sciences, University of Southern Queensland, Darling Heights, QLD, Australia.
Kirsten Coupland, Hunter Medical Research Institute, New Lambton Heights, NSW, Australia. School of Biomedical Sciences and Pharmacy, The University of Newcastle, Callaghan, NSW, Australia. Priority Research Centre for Stroke and Brain Injury, The University of Newcastle, Callaghan, NSW, Australia.
Murielle G Kluge, School of Biomedical Sciences and Pharmacy, The University of Newcastle, Callaghan, NSW, Australia. Centre for Advanced Training Systems, The University of Newcastle, Callaghan, NSW, Australia.
Angela Smith, HNE Health Libraries, Hunter New England Local Health District, New Lambton, NSW, Australia.
Sue Bowden, Consumer Investigator, Moon River Turkey, Bathurst, NSW, Australia.
Michael Nilsson, Hunter Medical Research Institute, New Lambton Heights, NSW, Australia. Centre for Rehab Innovations, The University of Newcastle, Callaghan, NSW, Australia. LKC School of Medicine, Nanyang Technological University, Singapore.
Frederick Rohan Walker, Hunter Medical Research Institute, New Lambton Heights, NSW, Australia. School of Biomedical Sciences and Pharmacy, The University of Newcastle, Callaghan, NSW, Australia. Priority Research Centre for Stroke and Brain Injury, The University of Newcastle, Callaghan, NSW, Australia. Centre for Advanced Training Systems, The University of Newcastle, Callaghan, NSW, Australia. Centre for Rehab Innovations, The University of Newcastle, Callaghan, NSW, Australia.
This study was supported by the NHMRC Centre of Research Excellence in stroke rehabilitation and recovery; HMRI MRSP Infrastructure Funding Brain and Mental Health Program; and the University of Newcastle Priority Research Centre for Stroke and Brain Injury.
Authors’ Statement of Conflict of Interest and Adherence to Ethical Standards Authors Madeleine Hinwood, Marina Ilicic, Prajwal Gyawali, Kirsten Coupland, Murielle G. Kluge, Angela Smith, Sue Bowden, Michael Nilsson, and Frederick Rohan Walker declare that they have no conflict of interest.
M.H. conceived and designed the study, collected and analysed the data, and drafted and revised the paper. M.I. collected and analysed the data, and drafted and revised the paper. P.G., K.C., and M.K. collected and analysed the data and revised the draft paper. A.S. designed and developed the systematic review strategy. S.B. provided consumer advocacy and revised the draft paper. M.N. and F.R.W. conceived the study, initiated the collaborative project, and revised the paper.
Ethical Approval This is a review of published literature, as such ethics approval is not required.
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Aug 21, 2019
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First published on ARNI Institute for Stroke Rehabilitation website
A change in cognitive ability is common after a stroke. Did you know that as many as two-thirds of stroke survivors may experience cognitive impairment as a result of their stroke.? If this is you, or you know someone who seems possibly to be going through such difficulties, here’s 18 steps you can take to try and improve cognition difficulties after stroke:
Put simply, cognition is thinking; it is the processing, organising and storing of information – an umbrella term for all of the mental processes used by your brain to carry you through the day, including perception, knowledge, problem-solving, judgement, language, and memory. The brain’s fantastic complexity means that it can collect vast amounts of information from your senses (sights, sounds, touch, etc) and combine it with stored information from your memory to create thoughts, guide physical actions, complete tasks and understand the world around you.
A stroke can affect the way your brain understands, organises and stores information. This brain injury can result in damage to the areas of the brain that are responsible for perception, memory, association, planning, concentration, etc. The severity and localisation of the stroke will effect the type and level of difficulties experienced by an individual, and will vary from person to person.
It can be difficult to plan and organise daily tasks. The brain is constantly working in the background, allowing us to complete a task based on prior knowledge, experience, and learned behaviour.
You don’t have to consciously think how to boil the kettle, change TV channels or put on your socks before your shoes: you just do it. But damage to the brain can result in problems with these planning and execution mechanisms.
You might not be able to think how to do a simple task, or you may get the sequence wrong (for example, shoes before socks). You might have trouble with orientation, which could include not knowing the date, day of the week, or even who you are with. Problem-solving too can become difficult. Making decisions, solving problems, understanding numbers and managing money can be a challenge.
Good cognitive function also relies on memory. The brain uses 2 types of memory to hold information, the long and short term memory. Short-term memory is the temporary store for small amounts of information. This information is kept readily available and can be recalled quickly. For example, a phone number can be remembered long enough for you to dial it. Long-term memory is where you keep your experiences, thoughts and feelings from the past and things stored here can be stored indefinitely. Memory problems could result in difficulty storing or recalling information. This could include problems remembering appointments, important dates or in the case of short term memory, what you were about to do, or what somebody just said to you.
Problems with concentration are common. Concentration is required for effective cognitive function, as many of your thinking process require concentration. Concentration requires our brain to filter out much of the information coming in from your conscious thinking, so you are not distracted by it.
Stroke can impact on this ability because of damage to the areas of the brain responsible for this, and also because tiredness, pain and emotional problems have an effect of the ability to stay focused and concentrate. This could result in difficulties when trying to follow a television programme, or conduct a conversation with a friend. Multi-tasking too is difficult.
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Key takeaways.
1. A stroke is a serious, life-threatening medical condition that happens when the blood supply to part of the brain is cut off. 2. Training and exercising a stroke survivor's brain is known as stroke rehabilitation. 3. Memory exercises are a fundamental part of stroke rehabilitation, helping to retrain the brain and improve cognitive function that may have been affected by the stroke.
1. What Are The Best Brain Exercises For Stroke Recovery? 2. What Are The Benefits Of Cognitive Exercises For Stroke Patients? 3. How Do You Train And Exercise Your Brain After A Stroke 4. How Effective Are Brain Stroke Recovery Exercises? 5. What Are Cognitive Therapy Activities For Stroke Victims And Survivors? 6. What Cognitive Activities For Adults After Stroke Are Most Effective? 7. How Do Stroke Cognitive Rehabilitation Activities Work? 8. Frequently Asked Questions About Brain Exercises For Stroke Recovery
A stroke is a serious, life-threatening medical condition that happens when the blood supply to part of the brain is cut off. Strokes occur when a blood clot blocks the flow of blood and oxygen to the brain. These blood clots are typically the result of atherosclerosis, or arteries narrowed or blocked over time by fatty deposits. This is the most common type of stroke. Less common are hemorrhagic strokes, where a blood vessel supplying the brain bursts.
People who survive a stroke are often left with long-term problems caused by an injury to their brain . They will face challenges with thinking, reasoning, awareness, and memory. If help is obtained over time, the brain retains some function but needs to reorganize itself. This journey to recovery is arduous and involves relearning skills, improving physical coordination, and maintaining cognitive functions.
The best exercises for stroke recovery focus on cognitive rehabilitation, including problem-solving activities like puzzles and board games, which enhance cognitive flexibility and decision-making skills . These exercises play a crucial role in helping individuals regain cognitive functions affected by stroke, such as memory, problem-solving skills, processing speed, and attention span, ultimately aiding in their recovery journey.
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Cognitive exercises play a crucial role in the rehabilitation of stroke survivors, but they need to be practiced consistently to be most effective. Following a stroke, the brain is busy rewiring new pathways to bypass the affected areas – a process known as neuroplasticity. Functions are being rewired to new, healthy areas of the brain, to compensate for tissue damage sustained in the stroke.
Training and exercising a stroke survivor’s brain is known as stroke rehabilitation . These typically are a program of different therapies, designed for the survivor to help them with movement, speech, strength, and daily living skills post-stroke. The aim is to help them regain their independence and quality of life.
What’s involved in stroke rehabilitation is speech and language therapy , focused on improving communication skills affected by the stroke and common post-stroke issues such as swallowing difficulties, otherwise known as dysphagia.
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According to the National Library of Medicine, approximately 40% of patients suffer from functional impairment after stroke onset, and 15–30% experience severe motor, sensory, cognitive, perceptual, and/or language impairments.
Rehabilitation is vital for stroke survivors, and those who undergo consistent and professional rehabilitation tend to recover quickly . Studies have shown that rehabilitation exercise regimens applied soon after a stroke are effective. The programs will need to be tailored to the survivor and how they were affected, so that the correct areas are given the necessary attention.
Cognitive issues are often the most debilitating and difficult-to-address consequences of a stroke. A stroke survivor with memory and attention issues who engages in cognitive therapy, including puzzles and memory games , could experience improvements in their memory and concentration, allowing them to better manage daily tasks and activities.
One may question what the difference is between regular exercises and those intended for stroke patients. The answer lies in their intention. Pre-stroke exercises are typically general and aim to maintain overall health and well-being – cardio, strength training, and muscle toning, for example. In contrast, post-stroke exercises are more targeted, focusing on the rehabilitation and recovery of specific functions affected by the stroke. Post-stroke exercises often involve intensive therapy tailored to individual needs, such as speech therapy, physical therapy, and cognitive exercises.
Studies have shown that brain stroke recovery exercises can be highly effective in improving functional outcomes and quality of life for stroke survivors. Studies published in the Journal of Stroke found that intensive rehabilitation programs significantly improved motor function and activities of daily living in stroke patients. Another study published in the Journal of Neurologic Physical Therapy showed that cognitive rehabilitation can lead to improvements in memory, attention, and executive function in stroke survivors.
Cognitive therapy is designed to improve cognitive functions affected by the stroke, for example, memory, processing speed, problem-solving, language, and executive functions . The aim is to challenge the brain in a supportive way.
Cognitive therapy would include memory exercises, e.g., card games to improve short-term working memory; puzzles, computer games, and reading and summarizing to improve their attention, concentration, and information processing; reading, writing, and conversation practice to help with communication; drawing; navigation tasks to help with visual-spatial orientation, planning, and awareness; and problem-solving tasks to help improve planning and organization skills.
How do stroke cognitive rehabilitation activities work.
A 37-year-old stroke survivor participated in memory-based exercises as part of his rehabilitation program. He regularly played memory games and engaged in storytelling activities with his therapist. Over time, his short-term memory and cognitive function significantly improved . He was able to recall important information, make decisions more confidently, and communicate more effectively with his family and healthcare providers.
Family members can play a crucial role in implementing these activities and supporting stroke rehabilitation. They can be educated on the importance of consistency and patience, as progress may be gradual.
Music stimulation therapy can benefit stroke survivors by engaging multiple areas of the brain. Listening to music activates the auditory cortex , which processes sound, while also stimulating areas responsible for memory and emotions. This stimulation can enhance cognitive functions such as memory, attention, and executive function. Additionally, music can evoke emotional responses that may help reduce stress and anxiety, which are common after a stroke.
Some examples of music-based exercises at home include listening to familiar music, such as the stroke survivor’s favorite songs or music from their past. This can evoke memories and emotions, stimulating cognitive function. Caregivers and guardians can sing along to these songs with the patient, to further engage the areas of the brain responsible for these functions.
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An overall change in daily routines is crucial in stroke recovery to promote brain retraining and maximize rehabilitation outcomes.
The most important are physical activity and cognitive stimulation . Incorporating regular physical activity into daily routines can improve blood flow to the brain, promote neuroplasticity, and enhance overall brain health. Activities like walking, yoga, or tai chi can be beneficial.
As for mentally stimulating activities, these include reading, puzzles, or learning new skills, which can help retrain the brain and improve cognitive function . These activities should be challenging but achievable to promote brain plasticity.
Apps and other digital tools can assist in cognitive rehabilitation post-stroke by providing accessible and engaging ways to improve cognitive functions. These tools can offer personalized exercises, real-time feedback, and progress tracking, making rehabilitation more efficient and effective .
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The best exercises for stroke recovery focus on cognitive rehabilitation, including problem-solving activities like puzzles and board games, which enhance cognitive flexibility and decision-making skills. These exercises play a crucial role in helping individuals regain cognitive functions affected by stroke, such as memory, problem-solving skills, processing speed, and attention span, ultimately aiding in their recovery journey.
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BMC Neurology volume 13 , Article number: 67 ( 2013 ) Cite this article
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Coping style is one of the determinants of health-related quality of life after stroke. Stroke patients make less use of active problem-oriented coping styles than other brain damaged patients. Coping styles can be influenced by means of intervention. The primary aim of this study is to investigate if Problem Solving Therapy is an effective group intervention for improving coping style and health-related quality of life in stroke patients. The secondary aim is to determine the effect of Problem Solving Therapy on depression, social participation, health care consumption, and to determine the cost-effectiveness of the intervention.
We strive to include 200 stroke patients in the outpatient phase of rehabilitation treatment, using a multicenter pragmatic randomized controlled trial with one year follow-up. Patients in the intervention group will receive Problem Solving Therapy in addition to the standard rehabilitation program. The intervention will be provided in an open group design, with a continuous flow of patients. Primary outcome measures are coping style and health-related quality of life. Secondary outcome measures are depression, social participation, health care consumption, and the cost-effectiveness of the intervention.
We designed our study as close to the implementation in practice as possible, using a pragmatic randomized trial and open group design, to represent a realistic estimate of the effectiveness of the intervention. If effective, Problem Solving Therapy is an inexpensive, deliverable and sustainable group intervention for stroke rehabilitation programs.
Nederlands Trial Register, NTR2509
Peer Review reports
Stroke is an increasing public health problem in the Netherlands: every year, 41,000 people suffer from stroke and over 3% of the total health care costs are related to the treatment of stroke and its consequences [ 1 ]. The mortality rate after stroke is 30% and is likely to decrease, which will cause an increase in morbidity [ 2 ]. Almost 50% of stroke survivors experience consequences in daily life that result in a lowered health-related quality of life (HR-QoL) [ 1 ]. The World Health Organization Quality of Life (WHOQOL) Group defines quality of life as “individuals’ perceptions of their position in life in the context of the culture and value systems in which they live and in relation to their goals, expectations, standards and concerns [ 3 ]. HR-QoL refers to the health-related aspects of quality of life. On average, utility scores of HR-QoL after stroke range from 0.47 to 0.68 (a utility score equal to death is 0.0 and full health 1.0), which is substantially lower than the value of a healthy reference population (utility score of 0.93) [ 4 , 5 ]. HR-QoL after stroke is predicted by functional constraints, age, gender, and psychosocial factors, like socioeconomic status, depression, and coping style [ 4 , 6 – 8 ]. Functional constraints, age, gender, and socioeconomic status cannot or are difficult to change, but coping style could be targeted. The question then becomes if HR-QoL after stroke could be improved through a coping style intervention. If this is possible, a secondary question would be how such improvement relates to depression, health care consumption, and costs.
A common definition of coping style is someone’s preferred way of dealing with different situations. Several coping styles can be distinguished, such as active, passive, and avoidant coping. Wolters (2010) shows that in traumatic brain-injured (TBI) patients, higher HR-QoL in the long term is predicted by an increase in active problem-focused coping style and a decrease in passive emotion-focused coping style. Unfortunately, in this population of TBI patients the active coping decreases over time, while passive coping increases [ 9 ]. This suggests that if the decrease of active coping can be stopped, there is room for improvement in HR-QoL. Stroke patients make even less use of active, problem-oriented coping styles compared to other brain damaged patients [ 10 ]. Furthermore, Darlington (2007) shows that in stroke patients, coping becomes more important in determining HR-QoL over time, while the importance of general functioning decreases [ 11 ]. This would mean that long term HR-QoL could benefit from improved coping.
Coping styles can be influenced by several interventions. Backhaus (2010) shows that an intervention aimed at changing maladaptive coping styles positively influenced psychosocial functioning of TBI patients [ 12 ]. However, HR-QoL was not measured in this study. No research is found that investigated an intervention aimed at improving HR-QoL through the change of maladaptive coping styles in stroke patients. We therefore set out to investigate whether Problem Solving Therapy (PST), which aims at active problem-focused coping, might improve HR-QoL in stroke patients. PST has been proved effective in other patient populations [ 13 , 14 ]. In stroke patients, PST has been shown successful for the prevention of post stroke depression [ 15 ]. Effects on coping style and HR-QoL have not been investigated yet.
The primary aim of this study is to investigate whether PST is an effective group intervention for improving active problem-focused coping style and HR-QoL in stroke patients. The secondary aim is to determine the effect of PST on depression, social participation, health care consumption, and the cost-effectiveness of the intervention. The effectiveness of the therapy will be investigated in an open group design, which has not been used in PST research before. PST will be added to the standard care just before the end of the rehabilitation program, as at this moment a relapse in HR-QoL is frequently observed, when patients cannot rely on their therapists anymore [ 16 ]. By teaching patients to actively cope with stressful situations, through adapting and realizing their goals, we expect that patients will use more effective coping styles, which consequently may prevent the relapse in HR-QoL, and possibly increase HR-QoL in the long term. With regard to the secondary aims of this study, we expect the incidence of depression to decrease, social participation to improve, and health care consumption to decrease, resulting in a favorable cost-effectiveness ratio for the intervention.
The effectiveness of PST for stroke patients will be evaluated in a multicenter pragmatic randomized controlled trial (RCT) with one year follow-up, with the intervention performed in the daily practice of a sub-acute outpatient stroke rehabilitation program. As such, the potential effects of the intervention have a good external validity, which allows us to calculate the cost-effectiveness of the therapy compared with standard care.
The study will be performed in Rijndam Rehabilitation Center in collaboration with Erasmus MC, both in the Netherlands, and in Ghent University Hospital in Belgium. Patients are invited by their rehabilitation physician to participate in the study. Before the start of the study, patients need to sign the informed consent form. Data will be collected at four time points by one of three research psychologists. T0 is the baseline measurement, performed within three weeks before the start of the intervention phase. T1 will be performed within ten days after the intervention phase, T2 six months and T3 twelve months after the intervention phase (Figure 1 ). The measurements will be performed in the rehabilitation center or at the patients’ home in a face-to-face interview. The study has been approved by the Medical Ethics Committee of Erasmus MC University Medical Center and the Ethics Committee of Ghent University Hospital.
Design of the randomized controlled trial.
We strive to include 200 stroke patients. Inclusion criteria are: stroke (including subarachnoid hemorrhage), age between 18 and 75 years, being treated in the outpatient rehabilitation phase, and being able to participate in group therapy. Exclusion criteria are: progressive neurological disorders, life expectancy less than one year, insufficient understanding of the Dutch language, excessive drinking or drug abuse, subdural hematomas, moderate and severe aphasia. The same criteria would apply to the implementation of PST in practice, which stresses the pragmatic character of the trial. The inclusion of patients started March 2011 and will end August 2013. The one-year follow-up of all patients will be finished by September 2014.
Patients are randomized to the intervention- or control condition using a stratified block randomization procedure with a block size of four. To ensure comparability between the two groups, patients are stratified per rehabilitation center. A member of the research group, who is not involved in the collection of the data, prospectively allocates the patients to the intervention- or control condition in a one-to-one ratio using an online random-number generator. To allow blinded randomization, the allocation information will be put in separate sealed envelopes which are consecutively numbered. At the end of the baseline measurement, the investigator opens the numbered envelop and informs the patient about the condition he or she is assigned to. The research psychologists who perform the baseline and follow-up measurements are blinded for treatment condition. The therapists who provide the intervention are not involved in the collection of the data. The investigator who will analyze the data is not involved in the collection of the follow-up measurements.
Patients who are assigned to the intervention condition will receive PST in addition to the standard rehabilitation program, which will start during the last eight weeks of outpatient treatment. PST is a widely used and practical intervention method, based on a general model of coping with stress [ 17 , 18 ]. The model states that having a chronic disease causes stressful daily problems, which increase the chance of experiencing psychological stress and depressive feelings. Therefore, the aim of PST is to improve the skills to cope with the stressful daily problems in life after stroke.
The intervention will be provided in an open group design, with a continuous flow of patients, which means that patients can enter the group every week and leave the group after eight sessions (Figure 2 ). The reason for this design is that it studies group therapy in its most feasible form, where patients start and end their programs at different time-points. If we had chosen to study the effect in closed groups, many patients in the similar stage of their programs are necessary. This would only be possible if patients are admitted to large scale rehabilitation centers, which is not the rehabilitation practice in The Netherlands, or patients would have to wait for a long time before entering the group. The open group design has some disadvantages. Patients may feel unsafe when they enter an already existing group. Furthermore, a continuous flow of patients is required to keep a balanced number of patients in the group. Therefore, interventions aimed at rare diseases cannot be studied with an open group design. However, for our population of stroke patients we do expect the design to be suitable and beneficial, because these patients are frequently seen in rehabilitation treatment. An open group design has several benefits as well. Advantages for the patients are that they do not have to wait until they can start with the intervention, they can share their experiences with other ‘experienced’ stroke patients, and there is room for interaction with many fellow patients. Other advantages are that the intervention is relatively easy to organize and implement in the daily practice of the rehabilitation center. This open group design has not been investigated in PST research yet.
Patient flow in an open group therapy.
The intervention in this study consists of eight group sessions of 1,5 hours a week, with homework exercises after each session. The group consists of a minimum of three and a maximum of six participants. PST is provided by one to three trained neuropsychologists per rehabilitation center. Solving problems will be structured, by dividing the problem solving process in four steps:
Define problem and goal;
Generating multiple solutions;
Considering the possible consequences of the solutions systematically and select the best solution;
Implement the solution and evaluate.
Each session starts with the sharing of experiences from the past week. Then, the model of problem solving will be repeated and explained. If there are some participants who are in the group for a couple of weeks already, they will be asked to explain the model to other new participants. Subsequently, one step of the model will be highlighted every week. With emphasis on this specific step, the model will be applied to one or more examples from the participants. Finally, the participants will be asked to practice the specific step at home by making a homework assignment. During the sessions, inadequate and irrational thoughts will be challenged by common cognitive interventions. A unique aspect of the intervention is the focus on the definition of the problem in the first step of the model. A clear definition of the problem will lead to a better understanding and more solutions to it.
Patients who are assigned to the control condition will receive the standard rehabilitation program, in order to be able to study the additional effect of the intervention to the standard rehabilitation program. This standard rehabilitation program consists of individualized amounts of treatment by a physical therapist, occupational therapist, speech therapist, psychologist, social worker, and rehabilitation physician, depending on the severity of stroke. On average, stroke patients in outpatient rehabilitation receive twelve hours of treatment a week during a nine week rehabilitation program.
Primary outcome measures are changes in task-oriented coping and psychosocial HR-QoL in patients in the intervention group in comparison with the control group. Coping style is measured using the Coping Inventory for Stressful Situations (CISS) and the short version of the Social Problem Solving Inventory-Revised (SPSI-R:SF). The CISS questionnaire consists of 48 questions and contains three subscales; Task-oriented coping, Emotion-oriented coping, and Avoidant coping. The subscale Avoidant coping consists of two subscales; Distraction and Social Diversion [ 18 , 19 ]. Because the PST aims at tasks, ‘Task-oriented coping’ is chosen as a primary endpoint; the other two subscales are used as secondary endpoints. The SPSI-R:SF questionnaire consists of ten questions about problem solving skills regarding daily situations. There are five subscales: Positive Problem Orientation, Rational Problem Solving, Negative Problem Orientation, Impulsivity/Carelessness Style, and Avoidance Style, and all are used as secondary endpoints in this trial [ 20 ].
HR-QoL is measured using the EuroQol (EQ-5D-5L) and the Stroke Specific Quality of Life Scale (SS-QoL-12). The EQ-5D is a generic questionnaire, and consists of five questions regarding mobility, self-care, daily activities, pain/complaints, mood, and a VAS scale. The five dimensions can be combined to one utility scale, representing the societal perspective of the general public [ 21 ]. The SS-QoL-12 is specifically developed for the population of stroke patients [ 22 ]. We will use the abbreviated version containing twelve items, which has been shown valid [ 23 ]. The questionnaire provides a total score and two sub scores: physical and psychosocial, of which the psychosocial sub-score is defined as the primary endpoint. The other HR-QoL scores are used as secondary endpoints.
Other secondary outcome measures are differences in depression, social participation, and health care consumption between patients in the intervention and control group. Additionally, the influence of cognitive functioning, personality characteristics, aphasia, type of stroke, side of stroke, level of functioning, and demographic characteristics on the outcomes will be assessed. Finally, the cost-effectiveness of the intervention will be calculated compared with standard care.
Depression is measured using the Center for Epidemiologic Studies Depression Scale (CES-D). This questionnaire consists of twenty items concerning depression, higher scores indicate more depressive symptoms [ 24 ].
Social participation is measured using the Impact on Participation and Autonomy (IPA). The questionnaire consists of five dimensions; Autonomy indoors, Family role, Autonomy outdoors, Social life and relationships, Work and education [ 25 ].
Health care consumption is measured using the Trimbos Questionnaire for Costs association with Psychiatric Illness (TiC-P). The questionnaire was developed for economic evaluation in mental health care, and measures health care consumption and productivity losses [ 26 ].
To determine the sample size for measuring differences between the intervention- and control group in coping style and HR-QoL, we searched for comparable effect sizes in the literature. With regard to coping style, there was no data available for this calculation. With regard to HR-QoL, Studenski (2005) measured an increase in HR-QoL after a physical therapy for stroke patients, with a long term effect size f ranging from 0.06 to 0.18 [ 27 ]. Because of the lack of more comparable data, we used this data and carefully estimated the effect size f to be 0.08. Considering the design of two groups and four repeated measurements, an expected correlation of 0.70, an alpha of 0.05, and a power of 0.80, we calculated a total required sample size of 132 patients based on the F-test. Because potential drop out is estimated at 0.30, we will strive to include 200 patients.
Demographic variables will be analyzed with an independent sample T-test for continuous variables, the Mann–Whitney U test for ordinal variables, and the chi-square test for categorical variables. Linear Mixed Models will be used to compare the repeated measurements between treatment groups, taking into account the correlation within and between subjects. We will create models for all the primary and secondary outcome variables, with time, group condition (intervention or control), and the interaction between these variables as predictors. Furthermore, we will control for variables that are accidentally not equally distributed between the two group conditions.
The cost-effectiveness of the intervention will be calculated by counting all the medical and non-medical costs, like productivity losses. The incremental cost-effectiveness ratio will be calculated by dividing the difference in total costs by the difference in quality-adjusted life years (QALYs). These QALYs will be calculated based on the EQ-5D questionnaire. The economic evaluation will be conducted according to the Dutch guidelines [ 28 ] and includes multivariate probabilistic sensitivity analyses. In the base case scenario the time horizon will be one year. If the effect is still present at one year follow up, a Markov model will be made to model a longer time horizon.
This study investigates the effect of PST on coping style and HR-QoL in stroke patients. In addition, the effect on depression, social participation, and health care consumption will be investigated, as well as the cost-effectiveness of the intervention. We will study the effectiveness of PST as close to the implementation in practice as possible, using a pragmatic trial design and an open group therapy. Any pragmatic trial has limitations; MacPherson (2004) argued that a pragmatic trial design cannot be used to determine the specific components of a treatment that caused an effect [ 29 ]. It may be possible that patients in the intervention group show improvement caused by the extra attention they receive and not so much by the assumed effective elements of the therapy; this attention effect may be considered a placebo effect. If we would like to distinguish between this ‘placebo effect’ and the effect of the specific treatment elements, the control group should have received a ‘sham therapy’. Such sham therapy would hinder the estimation of the effect of PST in practice, as in practice such additional effort would not take place. Therefore, one of the advantages of the pragmatic study design is that the external validity is better than using a sham-controlled design; the results will be generalizable to the normal rehabilitation setting [ 30 ]. The study population represents the normal stroke population in the outpatient phase of rehabilitation treatment, and the psychologists will provide the intervention to the patients just as they would do in practice. The results of a pragmatic trial are directly applicable to the usual care setting [ 31 ]. Moreover, if the intervention will prove effective, it will be easy to implement the intervention in the standard rehabilitation program, since it is already in use and the psychologists will already be trained. Other rehabilitation centers can use the therapy manual we developed.
We expect that patients who received PST will use more effective coping styles and experience a higher HR-QoL. Furthermore, we expect that patients after PST will show a decrease in depression score, an increase in social participation, and a decrease in health care consumption, which would lead to a reduction in the health care costs. We expect the intervention to be cost-effective, since the costs of the intervention are relatively low; one psychologist can train three to six patients at the same time. Darlington (2009) estimated the cost-effectiveness of an intervention aimed at coping strategies in stroke patients: the maximum costs for a single patient were 2500 euros, which will be lower if the therapy is provided in a group [ 32 ]. If PST will be proved effective for stroke patients in outpatient rehabilitation, the intervention will be an inexpensive, deliverable and sustainable group intervention that could be added to usual stroke rehabilitation programs.
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This study is funded by the National Initiative Brain and Cognition (NIHC 056-11-010), Stichting Coolsingel, and Erasmus MC Cost-Effectiveness Research.
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Marieke M Visser, Majanka H Heijenbrok-Kal & Gerard M Ribbers
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The authors declare that they have no competing interests.
All authors contributed to the development of the study protocol. AvtS adapted the PST-manual for the population of stroke patients. MMV implemented the therapy in the rehabilitation program. All authors read and corrected the draft version of this manuscript, and approved the final version.
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Visser, M.M., Heijenbrok-Kal, M.H., van ’t Spijker, A. et al. The effectiveness of problem solving therapy for stroke patients: study protocol for a pragmatic randomized controlled trial. BMC Neurol 13 , 67 (2013). https://doi.org/10.1186/1471-2377-13-67
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Stroke is an abrupt interruption of constant blood flow to the brain that causes loss of neurological function. The interruption of blood flow can be caused by a blockage, leading to the more common ischemic stroke, or by bleeding in the brain, leading to the more deadly hemorrhagic stroke. Ischemic stroke constitutes an estimated 87 percent of all stroke cases. Stroke often occurs with little or no warning, and the results can be devastating.
It is crucial that proper blood flow and oxygen be restored to the brain as soon as possible. Without oxygen and important nutrients, the affected brain cells are either damaged or die within a few minutes. Once brain cells die, they generally do not regenerate and devastating damage may occur, sometimes resulting in physical, cognitive and mental disabilities.
Ischemic stroke.
This is a warning sign of a possible future stroke and is treated as a neurological emergency. Common temporary symptoms include difficulty speaking or understanding others, loss or blurring of vision in one eye and loss of strength or numbness in an arm or leg. Usually these symptoms resolve in less than 10 to 20 minutes and almost always within one hour. Even if all the symptoms resolve, it is very important that anyone experiencing these symptoms call 911 and immediately be evaluated by a qualified physician.
Source: American Heart Association (AHA), Heart Disease and Stroke Statistics – 2010 Update.
Although they are more common in older adults, strokes can occur at any age. Understanding the factors that increase your risk of a stroke and recognizing the symptoms may help you prevent a stroke. Receiving early diagnosis and treatment may improve your chances for complete recovery.
Controllable or treatable risk factors for stroke include:
Uncontrollable risk factors include:
The range and severity of early stroke symptoms vary considerably, but they share the common characteristic of being sudden. Warning signs may include some or all of the following symptoms:
The effects of a stroke depend primarily on the location of the obstruction and the extent of brain tissue affected. One side of the brain controls the opposite side of the body, so a stroke affecting the right side will result in neurological complications on the left side of the body. A stroke on the right side may result in the following:
A stroke on the left side may result in the following:
Rehabilitation following a stroke may involve a number of medical specialists; but the early diagnosis of a stroke, its treatment or its prevention, can be undertaken by a neurosurgeon. Rapid and accurate diagnosis of the kind of stroke and the exact location of its damage is critical to successful treatment. Technical advances such as digital imaging, microcatheters and other neurointerventional technologies, the use of the operating microscope (microsurgery) and the surgical laser have made it possible to treat stroke problems that were inoperable a few years ago.
Ischemic stroke is treated by removing obstruction and restoring blood flow to the brain. The only U. S. Food and Drug Administration (FDA)-approved medication for ischemic stroke is tissue plasminogen activator (tPA), which must be administered within a three-hour window from the onset of symptoms to work best. Unfortunately, only 3- 5 percent of those who suffer a stroke reach the hospital in time to be considered for this treatment, and the actual use of tPA is considerably lower. This medication carries a risk for increased intracranial hemorrhage and is not used for hemorrhagic stroke.
Microcatheter-based surgical interventions for stroke may include the use of a small microcatheter, delivered through a larger guiding catheter inserted at the groin through a small incision. A microguidewire is used to navigate the microcatheter to the site of obstruction in the brain. Thrombolytic medication, such as tPA, can then be administered directly to the occluding thrombus. This kind of treatment, which delivers thrombolytic medication intraarterially, is more specific than IV (intravenous) tPA and consequently may require significantly lesser dosages of medication. The time limit to implement this type of intervention is also significantly (double) longer than that for IV TPA. Generally, only Comprehensive Stroke Care Centers offer this type of treatment.
The Merci Retriever, approved in 2004 by the FDA, is a corkscrew- shaped device used to help remove blood clots from the arteries of stroke patients. A small incision is made in the patient’s groin, into which a small catheter is fed until it reaches the arteries in the neck. At the neck, a small catheter inside the larger catheter is guided through the arteries into the brain, until it reaches the brain clot. A straight wire inside the small catheter pokes out beyond the clot and automatically coils into a corkscrew shape. It is pulled back into the clot, the corkscrew spinning and grabbing the clot. A balloon inflates in the neck artery, cutting off blood flow, so the device can pull the clot out of the brain safely. The clot is removed through the catheter with a syringe.
Penumbra is also a microcatheter-based system device, which works by an aspiration principle. It was approved by the FDA in 2008.
Stentriever devices are the newest generation of embolectomy devices for stroke. They are still in an investigative phase but work by breaking up the occluding clot, combined with aspiration or withdrawal.
Medications used to help prevent stroke in high-risk patients (especially those who have experienced a previous TIA or ischemic stroke) fall into two major categories: anticoagulants and antiplatelet agents.
Anticoagulants thin the blood and prevent clotting. Heparin acts quickly and is given intravenously or subcutaneously (beneath the skin) while a patient is in the hospital. Slower-acting warfarin can be given orally and is used over a longer period. Because these drugs affect the blood’s ability to clot, they require close monitoring by a physician.
Antiplatelet drugs prevent platelet aggregation. Platelets are specialized cells in the blood that initiate a healing process. Large numbers of platelets clump together to form a clot, which can sometimes block an artery or break loose, travel through the bloodstream and block a smaller artery. Antiplatelet drugs make platelets less sticky and less likely to form clots, reducing the risk of ischemic stroke in patients who have had TIA or prior ischemic stroke.
Carotid endarterectomy surgery (carotid endarterectomy, cea).
Patients will be given either a general or local anesthetic before surgery. In this procedure, the neurosurgeon makes an incision in the carotid artery in the neck and removes the plaque using a dissecting tool. Removing the plaque is accomplished by widening the passageway, which helps to restore normal blood flow. The artery will be repaired with sutures or a graft. The entire procedure usually takes about two hours. One may experience pain near the incision in the neck and some difficulty swallowing during the first few days after surgery. Most patients are able to go home after one or two days and return to work usually within a month. Patients should avoid driving and limit physical activities for a few weeks after surgery.
There are potential complications with carotid endarterectomy surgery, just as there are with any type of surgery. There is a 1-3 percent risk of stroke following surgery. Another fairly rare complication is the reblockage of the carotid artery, called restenosis. This may occur later, especially in cigarette smokers. Numbness in the face or tongue caused by temporary nerve damage is a possibility, but uncommon. This usually clears up in less than one month and most often does not require any treatment.
An alternative, newer form of treatment, carotid angioplasty and stenting (CAS), shows some promise in patients who may be at too high risk to undergo surgery. Carotid stenting is a neurointerventional procedure in which a tiny, slender metal-mesh tube is fitted inside the carotid artery to increase the flow of blood blocked by plaques. Access is gained through a small (0.5 cm) groin incision, but no incision is made in the neck. The stent is inserted following a procedure called angioplasty, in which the doctor guides a balloon-tipped catheter into the blocked artery. The balloon is inflated and pressed against the plaque, flattening it and reopening the artery. The stent acts as scaffolding to prevent the artery from collapsing or from closing up again after the procedure is completed.
There are several potential complications of endovascular treatment. The most serious risk from carotid stenting is an embolism caused by a disrupted plaque particle breaking free from the site. This can block an artery in the brain, causing a stroke. These risks are minimized using small filters called embolic protection devices in conjunction with angioplasty and stenting. There is also a slight risk of stroke due to a loose piece of plaque or a blood clot blocking an artery during or right after surgery. The risks are balanced against the advantages of a shorter occlusion time (10 seconds, as opposed to 30 minutes for endarterectomy), shorter anesthesia and a small leg incision.
Hyperperfusion, or the sudden increased blood flow through a previously blocked carotid artery and into the arteries of the brain, can cause a hemorrhagic stroke. Other complications include restenosis and short periods of medically treatable reduced blood pressure and heart rate. These risks are similar for CEA and CAS.
Hemorrhagic stroke usually requires surgery to relieve intracranial (within the skull) pressure caused by bleeding. Surgical treatment for hemorrhagic stroke caused by an aneurysm or defective blood vessel can prevent additional strokes. Surgery may be performed to seal off the defective blood vessel and redirect blood flow to other vessels that supply blood to the same region of the brain.
For a patient with a ruptured cerebral aneurysm, surgical elimination of the aneurysm is only the beginning. Intensive care recovery for the next 10-14 days is the rule, during which time a multitude of complications related to subarachnoid hemorrhage (SAH) can and do occur. At some time during that period (often immediately upon completion of surgery), cerebral angiography or a substitute study is done to document that the aneurysm has been eliminated. The first two to five days after SAH represent the greatest threat of brain swelling; at which time special measures (both medical and surgical) are used to diminish the effect of swelling on intracranial pressure. Near the end of this initial period, the risk period for delayed cerebral vasospasm begins and lasts the better part of the next 14 days. Intercurrent infections such as pneumonia are common, and hydrocephalus may develop.
Prior to surgery, the exact location of the subarachnoid hemorrhage or aneursym is identified through cerebral angiography images. An operation to “clip” the aneurysm is performed by doing a craniotomy (opening the skull surgically) and isolating the aneurysm from the normal bloodstream. In addition, a craniectomy, a surgical procedure in which part of the skull is removed and left off temporarily, may be done to help relieve increased intracranial pressure.
One or more tiny titanium clips with spring mechanisms are applied to the base of the aneurysm, allowing it to deflate. The size and shape of the clips is selected based on the size and location of the aneurysm. Clips are permanent, remain in place and generally provide a durable cure for the patient. Angiography is used to confirm exclusion of the aneurysm from the cerebral circulation and the preservation of normal flow of blood in the brain.
Neurointerventional procedures for cerebral aneurysm share the advantages of no incision made in the skull and an anesthesia time that is often dramatically shorter than for craniotomy and microsurgical clipping.
In endovascular microcoil embolization, a needle is placed into the femoral artery of the leg, and a small catheter is inserted. Utilizing x-ray guidance, the catheter is advanced through the body’s arterial system to one of the four blood vessels that feed the brain. A smaller microcatheter is fed into the aneurysm, and once properly positioned, a thin wire filament or “coil” is advanced into the aneurysm. The flexible, platinum coil is designed to conform to the shape of the aneurysm. Additional coils are advanced into the aneurysm to close the aneurysm from the inside. This prevents flow of blood into the aneurysm by causing a clot to form on the inside.
Balloon-assisted coiling uses a tiny balloon catheter to help hold the coil in place. Although this has been shown in several studies to increase risks, ongoing innovations in this relatively new technology has helped improve its efficacy. Combination stent and coiling utilizes a small flexible cylindrical mesh tube that provides a scaffold for the coiling. Intracranial stenting and other innovations are quite new, and endovascular technology is in a constant state of development. These adjuncts allow coiling to be considered for cerebral aneurysms that may not have an ideal shape for conventional coiling.
Recovery and rehabilitation are among the most important aspects of stroke treatment. As a rule, most strokes are associated with some recovery, the extent of which is variable. In some cases, undamaged areas of the brain may be able to perform functions that were lost when the stroke occurred. Rehabilitation includes physical therapy, speech therapy and occupational therapy. This type of recovery is measured in months to years.
The AANS does not endorse any treatments, procedures, products or physicians referenced in these patient fact sheets. This information is provided as an educational service and is not intended to serve as medical advice. Anyone seeking specific neurosurgical advice or assistance should consult his or her neurosurgeon, or locate one in your area through the AANS’ Find a Board-certified Neurosurgeon online tool.
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IMAGES
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COMMENTS
More than half of all stroke survivors experience a post-stroke cognitive impairment. This may affect many functions, including memory, problem solving skills, and the ability to think clearly, among others. However, survivors can often improve their mental aptitude by practicing cognitive exercises for stroke patients.
Many other thinking processes happen without us being aware of them, known as automatic processes. Together, many of these automatic processes are known as executive function. Executive function is about planning and problem-solving. It includes all the things that allow us to organise, make decisions and know when we need to do something.
same. More than two-thirds of stroke survivors receive rehabilitation services after leaving the hospital. Effective rehabilitation is an essential part of stroke care. Stroke rehabilitation requires a sustainable and coordinated effort from a team with the patient and the patient's goals at the center. In addition to the patient, the team ...
This raises the question whether the intervention should be adapted to increase and prolong the effects found. It may be useful to invite participants for more sessions or a refreshment session 6 months post intervention. ... The effectiveness of problem solving therapy for stroke patients: study protocol for a pragmatic randomized controlled ...
Decision making is defined as the process of examining possibilities, risks, uncertainties, and options, comparing them, and choosing a course of action. 1, 2 Decisions based on erroneous assessments may result in incorrect patient and family expectations, and potentially inappropriate advice, treatment, or discharge planning (eg, longer length ...
Percent of Users Identified As Recovering from Stroke: 40%. 6. Do clock math: Stroke can affect number skills, math skills, and word finding. This task helps improve time-based calculation skills by answering math questions associated with clocks. Individuals Assigned: 6,701 Percent of Users Identified As Recovering from Stroke: 37%. 7.
problem-solving refers to the "process of finding solutions to specific problems".13 Problem-solving therapy (PST) is an intervention in which patients are taught to increase structure in solving problems and flexibility by using different coping strategies in various situations. In patients with stroke, PST has
Example strategy games for stroke patients include: Carcassonne: a puzzle-based game that can challenge visuospatial skills and problem-solving. Chess: a traditional game requiring planning, judgement and reasoning. Catan: a building and trading game requiring constant cognitive flexibility and social skills.
The primary aim of this study is to investigate if Problem Solving Therapy is an effective group intervention for improving coping style and health-related quality of life in stroke patients. The secondary aim is to determine the effect of Problem Solving Therapy on depression, social participation, health care consumption, and to determine the ...
TTES Newsletter: Monthly newsletter provides patients and caregivers information on stroke-related research and resources. Stroke Family Warmline 1-888-478-7653: Connects stroke survivors and their families with specially trained ASA team members — some of whom are stroke family caregivers — for support, information or just a listening ear.
Our framework guided the design of the research questions, literature search, identification of studies, and the collation of results. ... Problem-solving therapy did not produce a significant change in overall problem-solving (SPISR; proxy measure for emotional distress). ... However, a high proportion of stroke patients have cognitive or ...
Making decisions, solving problems, understanding numbers and managing money can be a challenge. Good cognitive function also relies on memory. The brain uses 2 types of memory to hold information, the long and short term memory. Short-term memory is the temporary store for small amounts of information. ... Stroke can impact on this ability ...
ut them. If you're finding it hard, tell someone. Make it clear how they. port you can get.2 Don't be too hard on yourselfHaving cognitive problems after a stroke i. nothing you can control or need to feel bad about. A stroke is a major injury to your br. in, so it's going to take time for it to.
The following are some games that are helpful in stroke recovery cognitive exercises. Lumosity: This brain training app offers a variety of games designed to improve memory, attention, and problem-solving skills. Games like "Train of Thought" and "Memory Matrix" are particularly effective for cognitive exercise.
Coping style is one of the determinants of health-related quality of life after stroke. Stroke patients make less use of active problem-oriented coping styles than other brain damaged patients. Coping styles can be influenced by means of intervention. The primary aim of this study is to investigate if Problem Solving Therapy is an effective group intervention for improving coping style and ...
Stroke Practice Questions. (Asterisks*** indicate correct response) 1. A person presenting with a left lower extremity weakness most likely involves which vascular territory? a. the anterior cerebral artery***. b. the middle cerebral artery. c. the posterior cerebral artery.
The primary aim of this study is to investigate if Problem Solving Therapy is an effective group intervention for improving coping style and health-related quality of life in stroke patients.
Nurses provided information, reassurance and problem solving advice using a standardized checklist of topics: Clark 2003, 54 Australia: 62 community stroke patients and spouses: 32 intervention, 30 control. 1) Stroke information package covering stroke consequences, secondary prevention, coping and social support services: A: RCT: 3: S
1) Problem Statement/Research Question and Background. Stroke has been well-known as the most common cause of disability and death worldwide. Every year there are estimated to be 15 million of people who have experienced a stroke [1]. Loss of hand mobility is observed on most stroke patients, which inhibits their activities of daily living (ADL ...
The Health Equity and Actionable Disparities in Stroke: Understanding and Problem-Solving (HEADS-UP) symposium—a collaborative initiative with the American Stroke Association and National Institute of Neurological Disorders and Stroke (NINDS) established in 2020—is the first-ever annual multidisciplinary scientific forum focused on ...
Stroke is a leading cause of serious long-term disability, with an estimated 5.4 million stroke survivors currently alive today. In 2010, stroke cost about $73.7 billion in both direct and indirect costs in the U.S. alone. Source: American Heart Association (AHA), Heart Disease and Stroke Statistics - 2010 Update. Risk Factors
Quinn E, LeLaurin J, Eliazar-Macke N, Orozco T, Montague M, Freytes I and Uphold C (2023) Effect of a telephone and web-based problem-solving intervention for stroke caregivers on stroke patient activities of daily living: A randomized controlled trial, Clinical Rehabilitation, 10.1177/02692155231157301, 37:8, (1062-1073), Online publication ...