Actively Recruiting
Investigation of the Effects of Visual-Motor Based Training on Upper Extremity Functions in Individuals With Stroke
Led by Baskent University · Updated on 2025-09-04
38
Participants Needed
1
Research Sites
17 weeks
Total Duration
On this page
Sponsors
B
Baskent University
Lead Sponsor
B
Baskent University Ankara Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study is to investigate the effects of visual-motor based training and physiotherapy program on upper extremity functions in individuals with stroke and to compare with physiotherapy program.
CONDITIONS
Official Title
Investigation of the Effects of Visual-Motor Based Training on Upper Extremity Functions in Individuals With Stroke
Who Can Participate
Eligibility Criteria
You may qualify if you...
- At least 6 months have passed since the cerebrovascular event
- Aged between 18 and 75 years
- First-time stroke
- Scoring 24 or higher on the Standardized Mini Mental Test (SMMT)
- Upper extremity functioning at Stage 4 or above according to the Brunnstrom Staging
- Shoulder, elbow, wrist, and finger muscle tone at or below a score of 2 on the Modified Ashworth Scale (MAS)
- Shoulder joint range of motion of at least 1206
- Ability to stand independently
You will not qualify if you...
- Presence of hemispatial neglect syndrome
- Ataxia due to posterior circulatory ischemia
- Bilateral involvement (bilateral hemiparesis)
- Botulinum toxin injection in the last three months
- Physiotherapy treatment within the last 6 months
- Orthopedic problems such as shoulder subluxation, shoulder pain, or contractures in the hand or wrist
- Previous upper extremity or thoracic surgery
- Vision problems related to stroke (hemianopsia)
- Color blindness
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Başkent University
Ankara, Türkiye, Turkey (Türkiye), 06490
Actively Recruiting
Research Team
A
Ayşegül Aykul, MSc
CONTACT
Z
Zeliha Özlem Yürük, Prof Dr
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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