NCT07787013

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. 1.To find out if young stroke survivors use and engage with the computer-based treatment.
  2. 2.To learn about stroke survivors' experiences and feelings when using the treatment.
  3. 3.To see if this treatment influences stroke survivors' perceived readiness to return to work.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
25mo left

Started Nov 2026

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 14, 2026

Completed
12 days until next milestone

First Posted

Study publicly available on registry

August 26, 2026

Completed
2 months until next milestone

Study Start

First participant enrolled

November 2, 2026

Expected
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 30, 2027

1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

November 30, 2028

Last Updated

August 26, 2026

Status Verified

August 1, 2026

Enrollment Period

1.1 years

First QC Date

August 14, 2026

Last Update Submit

August 24, 2026

Conditions

Keywords

StrokeCerebrovascular AccidentCVAReturn to workOccupational TherapyCognitive interventionsComputer-Based Cognitive InterventionsCBCR

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

OTHER

Feasibility intervention

Other: RehaCom online

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.

RehaCom online

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Stroke

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular Diseases

Study Officials

  • Dewhurst

    Bournemouth University

    STUDY DIRECTOR
  • Collins

    Bournemouth University

    STUDY DIRECTOR

Central Study Contacts

Preetee Gokhale, M.O.Th

CONTACT

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

Locations