Fact CheckerSign in

NCT07127536Recruiting

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

Effects of the Cognitive Orientation to Daily Occupational Performance (CO-OP) Approach on Occupational Performance and Executive Function in Adults With Stroke: A Randomised Controlled Trial

Source: ClinicalTrials.gov · Last updated 22 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
66 (estimated)
First submitted
11 Aug 2025
Start date
1 Jan 2024
Primary completion date
31 Dec 2025
Lead sponsor
Hacettepe University
Diseases
Stroke
NCT number
NCT07127536

What you commit to

  • Study type: Interventional
  • Planned participants: 66
  • From 1 Jan 2024 to the primary completion date, 31 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Having any orthopedic, psychological, or neurological disorder other than stroke
  • Having cognitive impairment (Mini-Mental State Examination score ≤ 24)

Other

  • Having moderate to severe aphasia
  • Not willing to participate in the study

Who the study is looking for

  • 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

Age in the registry: 40 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Etlik City Hospital
Coordinator of this site? Confirm its status
AnkaraTurkey (Türkiye)Recruiting

This page is information, not medical advice. Discuss any trial with your doctor.