The Effect of Mirror Therapy Applied to Stroke Patients on Motor-Sensory Status and Quality of Life
NCT ID: NCT06963762
Last Updated: 2025-05-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
NA
60 participants
INTERVENTIONAL
2025-05-31
2026-01-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Mirror Therapy in Stroke
NCT05312905
Mirror Therapy Combined With TENS for Motor Recovery in Paretic Upper Limbs of Chronic Stroke Patients
NCT06770712
Virtual Reality Based Mirror Therapy
NCT06152328
The Effects of Motor Imagery Training and Physical Practice on Upper Extremity Motor Function in Patients With Stroke
NCT05526612
Multiple Effects of Dual-Task Focused Training in Individuals with Chronic Stroke
NCT06559930
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
SEQUENTIAL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
conventional rehabilitation group
Conventional rehabilitation will be applied
Conventional rehabilitation will be applied for 30 minutes, 4 times a week for 4 weeks.
group receiving mirror therapy along with conventional rehabilitation
Mirror therapy will be applied along with conventional rehabilitation
In addition to conventional rehabilitation, patients in the experimental group will receive mirror therapy for 30 minutes, 4 times a week for 4 weeks.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Conventional rehabilitation will be applied
Conventional rehabilitation will be applied for 30 minutes, 4 times a week for 4 weeks.
Mirror therapy will be applied along with conventional rehabilitation
In addition to conventional rehabilitation, patients in the experimental group will receive mirror therapy for 30 minutes, 4 times a week for 4 weeks.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Being over the age of 18,
3. Having sufficient communication skills to answer oral and written questions and follow instructions,
4. Having been diagnosed with a stroke and at least 6 days have passed since it occurred,
5. Not having severe vision problems,
6. Not having a vertigo problem,
7. Not having been diagnosed with epilepsy,
8. Upper extremity Stage 2 and above in Brunnstrom staging
9. Lower extremity Stage 2 and above in Brunnstrom staging
Exclusion Criteria
2. Upper extremity Stage 2 and below in Brunnstrom staging
3. In Brunnstrom staging, Lower extremity Stage 2 and below
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ataturk University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
AHMET ŞİMŞEK
PhD student
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
ATAÜNİ-SBE-AS-03
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.