Actively Recruiting

Phase Not Applicable
Age: 40Years - 80Years
All Genders
NCT06750692

Comparison of the Effects of Mirror Therapy,rTMS and Robotic-assisted Hand Therapy in Stroke Patients

Led by Afyonkarahisar Health Sciences University · Updated on 2026-03-12

120

Participants Needed

1

Research Sites

77 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of the study is to investigate the comparison of the effects of mirror therapy, Repetitive Transcranial Magnetic Stimulation and robot-assisted hand therapy added to conventional neurological rehabilitation on upper extremity function, quality of life and pain in stroke.

CONDITIONS

Official Title

Comparison of the Effects of Mirror Therapy,rTMS and Robotic-assisted Hand Therapy in Stroke Patients

Who Can Participate

Age: 40Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients diagnosed with hemiplegia after a cerebrovascular accident
  • Male or female patients aged 40 to 80 years
  • Stroke occurred at least 3 months prior
  • Voluntary participation with stable medical condition suitable for rehabilitation
  • Mini mental test score of 15 or higher
  • Neurologically stable patients
Not Eligible

You will not qualify if you...

  • Serious heart disease such as aortic stenosis, angina, hypertrophic cardiomyopathy, arrhythmia, or pacemaker
  • Uncontrolled hypertension
  • History of epilepsy or use of antiepileptic drugs
  • Presence of intracranial metal objects
  • Presence of intraauricular implants
  • Cognitive dysfunction
  • Peripheral nerve injuries in the upper extremity
  • Malignancy or active infection
  • Skin infections or open wounds where therapy is applied
  • Inflammatory diseases
  • Orthopedic injuries limiting effort capacity
  • Brain lesions or medication affecting seizure threshold
  • Increased intracranial pressure
  • Uncontrolled migraine
  • Severe hand spasticity (Modified Ashworth Scale score 3 or higher)
  • Contracture in the hand
  • Fracture or surgery on the affected side in the last 6 months
  • Severe visual impairment
  • Severe depression

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

Afyonkarahisar Health Sciences University

Afyonkarahisar, Turkey (Türkiye), 0300

Actively Recruiting

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Research Team

S

Sanberk Beklen, MD

CONTACT

S

Selma Eroglu, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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