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Recruiting NCT07127536

Effects of the CO-OP Approach on Occupational Performance and Executive Function in Adults With Stroke

Trial Parameters

Condition Stroke
Sponsor Hacettepe University
Study Type INTERVENTIONAL
Phase N/A
Enrollment 66
Sex ALL
Min Age 40 Years
Max Age 65 Years
Start Date 2024-01-01
Completion 2025-12-31
Interventions
CO-OP (Cognitive Orientation to daily Occupational Performance)Standard Occupational Therapy

Brief Summary

The purpose of this research study is to use the Cognitive Orientation to Daily Occupational Performance (CO-OP) approach with people who have experienced a stroke. This method helps individuals improve how they perform daily tasks by teaching them problem-solving strategies. This study will answer the following main questions: Does the CO-OP approach help participants perform their daily activities more easily? Does the CO-OP approach support thinking skills such as planning and attention? Researchers will look at changes in participants' daily activity performance and thinking skills before and after the CO-OP sessions. Participants will be randomly assigned to one of two groups: Complete simple tests before and after the sessions Practice real-life daily activities that are meaningful to them Intervention group: Will receive standard occupational therapy plus CO-OP sessions. The CO-OP sessions will take place 5 days a week for 4 weeks, with each session lasting 45 minutes. Control group: Will receive only standard occupational therapy as part of usual care.

Eligibility Criteria

Inclusion Criteria: * Being in the subacute phase after stroke (3 months \< stroke onset \< 2 years) * First-ever stroke * Brunnstrom stage 2 or above * Ability to read and write * Receiving rehabilitation services at Ankara Etlik City Hospital, Physical Medicine and Rehabilitation Hospital Exclusion Criteria: * Having any orthopedic, psychological, or neurological disorder other than stroke * Having moderate to severe aphasia * Having cognitive impairment (Mini-Mental State Examination score ≤ 24) * Not willing to participate in the study

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