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NCT06750692Completed

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

Comparison of the Effects of Mirror Therapy,Repetitive Transcranial Magnetic Stimulation and Robotic-assisted Hand Therapy Added to Neurological Rehabilitation on Upper Extremity Functions, Quality of Life and Pain in Stroke Patients

Source: ClinicalTrials.gov · Last updated 30 Jul 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
120 (actual)
First submitted
20 Dec 2024
Start date
20 Jan 2025
Primary completion date
20 Apr 2026
Lead sponsor
Afyonkarahisar Health Sciences University
Diseases
Stroke
NCT number
NCT06750692

What you commit to

  • Study type: Interventional
  • Participants enrolled: 120
  • From 20 Jan 2025 to the primary completion date, 20 Apr 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.

Prior treatment

  • intraauricular implants
  • have had a fracture or surgery on the hemiplegic side in the last 6 months

Other illness

  • significant comorbidities such as serious heart disease (aortic stenosis, angina, hypertrophic cardiomyopathy, arrhythmia, pacemaker) and uncontrolled hypertension
  • history of epilepsy, antiepileptic drug use
  • malignancy
  • active infection
  • skin infections or open wounds in the application area
  • inflammatory diseases
  • brain lesion or drug use history that may affect the seizure threshold
  • severe visual impairment

Other

  • intracranial metal objects
  • cognitive dysfunction
  • upper extremity peripheral nerve injuries
  • orthopedic injuries that may limit maximum effort capacity
  • increased intracranial pressure
  • uncontrolled migraine
  • severe spasticity in the hand (MAS≥3)
  • contracture in the hand
  • severe depression

Who the study is looking for

  • Patients who applied to Afyonkarahisar Health Sciences University Hospital Physical Medicine and Rehabilitation Polyclinic with the diagnosis of hemiplegia after a cerebrovascular accident in the inpatient ward or as an outpatient for neurological rehabilitation after taking the anamnesis and physical examination, who met the inclusion criteria and eliminated the exclusion criteria
  • Female and male patients between the ages of 40-80
  • stroke at least 3 months ago
  • voluntarily agreed to participate in the study regularly, whose health status is suitable for rehabilitation and who are medically stable
  • mini mental test score of 15 and above
  • Neurologically stable patient

Age in the registry: 40 years to 80 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
Afyonkarahisar Health Sciences University
Coordinator of this site? Confirm its status
AfyonkarahisarTurkey (Türkiye)Unknown status

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