NCT07546864Recruiting
Comparative Effects of Mirror Therapy and Cognitive Orientation to Daily Occupational Performance in Stroke: A Randomized Controlled Trial
Comparative Effects of Mirror Therapy, Cognitive Orientation to Daily Occupational Performance, and Conventional Occupational Therapy in Individuals With Stroke: A 3-Month Follow-Up Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 23 Apr 2026
Brief summary (registry, in English)
This study aims to compare the effectiveness of three rehabilitation approaches in individuals with stroke: mirror therapy (MT), cognitive orientation to daily occupational performance (CO-OP), and conventional occupational therapy (COT), all combined with robotic balance training. A total of 45 individuals with subacute and chronic stroke will be randomly assigned to one of three groups. Each group will receive 4 weeks of intervention (5 sessions per week), followed by a 3-month follow-up period. Outcomes related to motor function, somatosensory function, activities of daily living, participation, and quality of life will be assessed at baseline, after intervention, and at follow-up. The study aims to determine which intervention approach is more effective in improving functional outcomes in individuals with stroke.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 45 (estimated)
- First submitted
- 17 Apr 2026
- Start date
- Feb 2026
- Primary completion date
- May 2026
- Lead sponsor
- Hacettepe University
- Diseases
- Stroke
- NCT number
- NCT07546864
What you commit to
- Study type: Interventional
- Planned participants: 45
- From Feb 2026 to the primary completion date, May 2026
- 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
- Psychiatric conditions that may interfere with participation (e.g., depression, ongoing psychiatric treatment, low motivation)
Other
- \- Poor motor coordination or major medical problems that would prevent participation
- Presence of Wernicke's aphasia
- Botulinum toxin injection within the last 3 months
Who the study is looking for
- \- Individuals diagnosed with ischemic or hemorrhagic stroke
- Age 18 years and older
- Subacute (3-6 months post-stroke) or chronic stage (6-12 months post-stroke)
- Brunnstrom Motor Recovery Stage ≥3 for upper extremity, ≥4 for hand, and ≥4 for lower extremity
- Mini-Mental State Examination (MMSE) score ≥24
- No severe visual, orthopedic, or additional neurological impairments
- Not participating in another study during the research period
- Voluntary consent to participate in the study
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Bayburt State Hospital Coordinator of this site? Confirm its status | Bayburt | Turkey (Türkiye) | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.