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

Last updated: December 27, 2024
Sponsor: Afyonkarahisar Health Sciences University
Overall Status: Active - Recruiting

Phase

N/A

Condition

Stroke

Oral Facial Pain

Pain (Pediatric)

Treatment

Robotic-assisted hand therapy

Device: Low Frequency rTMS Protocol

Procedure: Mirror therapy

Clinical Study ID

NCT06750692
SBH2025
  • Ages 40-80
  • All Genders

Study Summary

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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients who applied to Afyonkarahisar Health Sciences University Hospital PhysicalMedicine and Rehabilitation Polyclinic with the diagnosis of hemiplegia after acerebrovascular accident in the inpatient ward or as an outpatient for neurologicalrehabilitation after taking the anamnesis and physical examination, who met theinclusion 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 issuitable for rehabilitation and who are medically stable

  • mini mental test score of 15 and above

  • Neurologically stable patient

Exclusion

Exclusion Criteria:

  • significant comorbidities such as serious heart disease (aortic stenosis, angina,hypertrophic cardiomyopathy, arrhythmia, pacemaker) and uncontrolled hypertension

  • history of epilepsy, antiepileptic drug use

  • intracranial metal objects

  • intraauricular implants

  • cognitive dysfunction

  • upper extremity peripheral nerve injuries

  • malignancy

  • active infection

  • skin infections or open wounds in the application area

  • inflammatory diseases

  • orthopedic injuries that may limit maximum effort capacity

  • brain lesion or drug use history that may affect the seizure threshold

  • increased intracranial pressure

  • uncontrolled migraine

  • severe spasticity in the hand (MAS≥3)

  • contracture in the hand

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

  • severe visual impairment

  • severe depression

Study Design

Total Participants: 120
Treatment Group(s): 3
Primary Treatment: Robotic-assisted hand therapy
Phase:
Study Start date:
December 27, 2024
Estimated Completion Date:
June 20, 2026

Study Description

Stroke is the second leading cause of death in adults and an important cause of long term disability. Functional limitations that develop in the post stroke period affect participants quality of life and activities of daily living. Today, despite advances in rehabilitation and new pharmacologic strategies, stroke related upper extremity function, quality of life and pain treatment may not always achieve the desired results. There are new approaches in stroke rehabilitation such as mirror therapy, Repetitive Transcranial Magnetic Stimulation, robot-assisted hand therapy. Three groups will take part in this study. All three groups will receive a total of 20 sessions of conventional neurological rehabilitation program 5 days a week for 4 weeks. In addition to the first group, a total of 20 sessions of upper extremity mirror therapy program will be applied for 4 weeks, 5 sessions per week. The second group will receive Repetitive Transcranial Magnetic Stimulation (rTMS) to the contralateral M1 upper extremity motor cortex region at low frequency (1Hz) and at an intensity of 100%-110 of the resting motor threshold, 5 sessions per week for a total of 20 sessions for 4 weeks. The third group will receive a total of 20 sessions of robot-assisted hand therapy using AMADEO (Tyromotion Austria) 5 days a week for 4 weeks.These three groups will be compared in terms of upper extremity function, quality of life and pain.Brunstroom, Mini Mental Test, Modified Ashworth Scale, Fugl Meyer Upper Extremity Motor Assessment Scale, Box Block Test, Nine Hole Pag Test, ABILHAND Stroke Hand Function Questionnaire, Stroke Impact Questionnaire, Stroke Specific Quality of Life Scale, Visual Analog Scale , LANNS neuropathic pain assessment scale, 4 Question Neuropathic Pain Questionnaire, Beck Depression Inventory, Beck Anxiety Scale, Pittsburgh Sleep Quality Index, MEP (motor evoked potential) measurement will be done . Participants will be evaluated by a physician twice at the beginning and at the end of treatment (4th week).

Connect with a study center

  • Afyonkarahisar Health Sciences University

    Afyonkarahisar, 0300
    Turkey

    Active - Recruiting

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.