Actively Recruiting
Comparative Effects of Mirror Therapy and Cognitive Orientation to Daily Occupational Performance in Stroke: A Randomized Controlled Trial
Led by Hacettepe University · Updated on 2026-04-23
45
Participants Needed
1
Research Sites
69 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Comparative Effects of Mirror Therapy and Cognitive Orientation to Daily Occupational Performance in Stroke: A Randomized Controlled Trial
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with ischemic or hemorrhagic stroke
- Age 18 years or older
- Stroke in subacute (3-6 months) or chronic (6-12 months) stage
- Brunnstrom Motor Recovery Stage ≥3 for upper extremity, ≥4 for hand, and ≥4 for lower extremity
- Mini-Mental State Examination score ≥24
- No severe visual, orthopedic, or additional neurological impairments
- Not participating in another study during this research
- Voluntary consent to participate
You will not qualify if you...
- Poor motor coordination or major medical problems preventing participation
- Presence of Wernicke's aphasia
- Botulinum toxin injection within the last 3 months
- Psychiatric conditions interfering with participation (e.g., depression, ongoing psychiatric treatment, low motivation)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Bayburt State Hospital
Bayburt, Merkez, Turkey (Türkiye), 69000
Actively Recruiting
Research Team
N
NURTEN BİLGİN, PhD Student
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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