Computer Based Cognitive Rehabilitation (CBCR) Intervention for Young Stroke Survivors' Return to Work
CBCR
A Non-randomised Feasibility Study Evaluating Use of a Computer-based Cognitive Rehabilitation (CBCR) Intervention Within Community Vocational Rehabilitation Pathway for Young Stroke Survivors.
1 other identifier
interventional
30
1 country
1
Brief Summary
Stroke can damage the brain, which may make it harder for survivors to think clearly, solve problems, and remember things. These changes in thinking can make it difficult for people to return to their jobs after a stroke. More and more, people are using computer-based exercises in rehabilitation and therapy to help with recovery. One such program, called RehaCom Online, is designed to help retrain the brain and improve decision-making and thinking skills. This project is looking at whether stroke survivors (aged 18-65) consider using RehaCom Online acceptable and feasible when used alongside regular occupational therapy care, to help improve their thinking and get back to work more quickly. The project will include people between the ages of 18 and 65 who are already receiving occupational therapy and whose therapy goals focus on return to work. Those who meet the study requirements will take part in a five-week course using the RehaCom Online software, in addition to their usual therapy sessions. They will also take tests to measure their attention, memory, and thinking skills and perceived work readiness. The main goals of the project are:
- 1.To find out if young stroke survivors use and engage with the computer-based treatment.
- 2.To learn about stroke survivors' experiences and feelings when using the treatment.
- 3.To see if this treatment influences stroke survivors' perceived readiness to return to work.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Nov 2026
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 14, 2026
CompletedFirst Posted
Study publicly available on registry
August 26, 2026
CompletedStudy Start
First participant enrolled
November 2, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
November 30, 2027
Study Completion
Last participant's last visit for all outcomes
November 30, 2028
August 26, 2026
August 1, 2026
1.1 years
August 14, 2026
August 24, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
RehaCom online assessment
Records a percentage increase in the module scores completed on RehaCom online.
RehaCom online assessment record will be reviewed on Day 1 and on day 35 of intervention .
Semi Structured interviews
Semi structured interviews focussing on subjective experience of RehaCom online use will be completed by the researcher and qualitative data will be recorded for analysis.
Between day 35 and day 42 of completing RehaCom online intervention.
Secondary Outcomes (5)
Behavioural Assessment of Dysexecutive Syndrome-DEX Questionnaire
Assessment will be completed on day 0 and between day 35 and day 42 of intervention
Montreal Cognitive Assessment
Assessment will be completed on day 0 and between day 35 and day 42 of intervention
Work Ability Index
Assessment will be completed on day 0 and between day 35 and day 42 of intervention
Motivation at work questionnaire
Assessment will be completed on day 0 and between day 35 and day 42 of intervention
Employment Readiness checklist
Assessment will be completed on day 0 and between day 35 and day 42 of intervention
Study Arms (1)
RehaCom online
OTHERFeasibility intervention
Interventions
Participants will use an online computer-based brain training programme called RehaCom Online (or alternatively called RehaCom) along with their regular therapy. They will engage with at least two 30 minutes training sessions per week for 5 weeks, with a total of 10 sessions. The may choose to engage with a maximum of five 30-minutes sessions per week for 5 weeks, with a total of 25 sessions. The frequency and duration will be personalised. Initial training on RehaCom online will be offered online and this will count as one session. The rest will be supervised remotely by the researcher using RehaCom Online software. Sessions will be completed independently in a location of participant's choosing, i.e. at home. Participants of the study will be able to contact the researcher via telephone, email or the RehaCom Online message function with a response time frame of 24-48 hours. Participants will have the flexibility to use rest breaks during the RehaCom training intervention.
Eligibility Criteria
You may qualify if:
- Ages 18-65 (working age)
- Score of 12 or more on a specific test of thinking called Behavioural Assessment of Dysexecutive Syndrome (BADS)
- Referred to NHS based services with a goal to return to work
- Can do assessments in English and use a computer
- Have a stable internet connection to access training
You may not qualify if:
- Have seizures
- Have vision problems specific to stroke
- Have trouble understanding English language due to their stroke symptoms
- Lack capacity to provide consent for participation
- Working in participating community rehabilitation services for stroke and willing to be involved in this study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Bournemouth University
Bournemouth, Dorset, BH88GP, United Kingdom
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Dewhurst
Bournemouth University
- STUDY DIRECTOR
Collins
Bournemouth University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 14, 2026
First Posted
August 26, 2026
Study Start (Estimated)
November 2, 2026
Primary Completion (Estimated)
November 30, 2027
Study Completion (Estimated)
November 30, 2028
Last Updated
August 26, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will not share