Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07546864

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Bayburt State Hospital

Bayburt, Merkez, Turkey (Türkiye), 69000

Actively Recruiting

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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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