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Not Yet RecruitingNCT06963762

The Effect of Mirror Therapy Applied to Stroke Patients on Motor-Sensory Status and Quality of Life

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Ataturk University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Purpose: The research will be conducted to evaluate the effect of Mirror Therapy applied to Stroke Patients on motor-sensory status and quality of life. Method: The research will be carried out as a randomized controlled experimental study at Bilecik Training and Research Hospital and Bozüyük State Hospital between 01.08.2024-01.05.2025. The population of the research consists of 350 people. Individuals will be distributed to the experimental (30) and control (30) groups by simple randomization method. In collecting research data; The patient introduction form, Brunnstrom Staging and SF-36 Quality of Life Scale will be administered to the patients in both groups by the researcher using face-to-face interview technique (pre-test). Patients in the experimental group will be informed about mirror therapy. In addition to conventional rehabilitation, patients in the experimental group will receive mirror therapy for 30 minutes, 4 times a week for 4 weeks. Patients in the control group will only receive conventional rehabilitation for 30 minutes, 4 times a week for 4 weeks. At the end of the 4th week, patients in both groups will be administered Brunnstrom Staging and SF-36 Quality of Life Scale (posttest). If both groups are discharged before 4 weeks, the planned practices will continue at home.

Conditions

Interventions

TypeNameDescription
BEHAVIORALConventional rehabilitation will be appliedConventional rehabilitation will be applied for 30 minutes, 4 times a week for 4 weeks.
BEHAVIORALMirror therapy will be applied along with conventional rehabilitationIn addition to conventional rehabilitation, patients in the experimental group will receive mirror therapy for 30 minutes, 4 times a week for 4 weeks.

Timeline

Start date
2025-05-01
Primary completion
2026-01-01
Completion
2026-01-01
First posted
2025-05-09
Last updated
2025-05-09

Source: ClinicalTrials.gov record NCT06963762. Inclusion in this directory is not an endorsement.