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Feasibility Study of Occupation-Based 'Remediation, Education, Adaptation, Promotion' (REAP) Program Among People With Stroke in Bang

Feasibility Study of Occupation-Based 'Remediation, Education, Adaptation, Promotion' (REAP) Program Among People With Stroke in Bang

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07272759
Enrollment
6
Registered
2025-12-09
Start date
2025-10-20
Completion date
2026-03-30
Last updated
2025-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Brief summary

Stroke causes major disability issues in Bangladesh and often leaves people unable to look after themselves, work, or participate in family and community life. Most stroke survivors in Bangladesh do not receive adequate rehabilitation, and existing services focus mainly on physical exercises, not on helping people return to meaningful activities. The REAP programme is a new therapy approach that remediates skills through structured training, educates patients and families on stroke management, adapts tasks or environments to make daily activities easier, and promotes participation in meaningful roles and activities. This study will test whether the REAP programme can be delivered successfully in a Bangladeshi rehabilitation centre, whether patients find it acceptable, and whether it helps people become more independent and improves quality of life.

Interventions

OTHEROccupation-Based 'Remediation, Education, Adaptation, Promotion' (REAP) Program

The REAP program consists of four core components designed to address the complex needs of stroke survivors: 1. Remediation 2. Education 3. Adaptation 4. Promotion

Sponsors

Centre for the Rehabilitation of the Paralysed, Bangladesh
CollaboratorOTHER
Tokyo Metropolitan University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Aged 18-64 years, * Diagnosed with stroke (ischemic/hemorrhagic) 3-24 months prior, * Medically stable and able to provide informed consent, * MoCA score ≥18.

Exclusion criteria

* Severe receptive aphasia, * Major psychiatric disorders, * Unstable medical conditions

Design outcomes

Primary

MeasureTime frameDescription
Barthel IndexFrom enrollment to 12 weeksAssesses independence in activities of daily living (ADLs).
Montreal Cognitive Assessment (MoCA)Enrollment to 12 weeksScreens for cognitive impairment.
Bangladeshi Occupational Self-Assessment - Short Form (BOSA-SF) (Enrollment to 12 weeksEvaluates perceived occupational competence and values within the local context.
Fugl-Meyer Assessment (FMA)Enrollment to 12 weeksAssesses motor recovery post-stroke
Occupational Balance QuestionnaireEnrollment to 12 weeksMeasures balance between different occupational areas in everyday life.
Life Satisfaction Questionnaire (LiSat-11)Enrollment to 12 weeksAssesses subjective life satisfaction across various domains
Zarit Caregiver Burden ScaleEnrollment to 12 weeksAssesses the level of burden experienced by informal caregivers

Countries

Bangladesh

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026