Actively Recruiting
The Effects of Augmented Reality Versus Virtual Reality
Led by Ankara Yildirim Beyazıt University · Updated on 2025-10-03
66
Participants Needed
1
Research Sites
95 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This randomized controlled trial aims to compare the effects of augmented reality (AR) and virtual reality (VR)-assisted treadmill gait training on balance and walking in individuals with stroke, within the framework of the International Classification of Functioning, Disability and Health (ICF). A total of 66 post-stroke patients will be randomly assigned to three groups: (1) VR group receiving gait training via C-Mill VR applications in addition to conventional physiotherapy, (2) AR group receiving gait training via C-Mill AR applications in addition to conventional physiotherapy, and (3) control group receiving a home exercise program alongside conventional physiotherapy. Participants will train for 45 minutes per day, five days a week, for three weeks. Outcome measures will include clinical, functional, cognitive, and spatiotemporal gait parameters to evaluate changes in balance and walking ability before and after the intervention.
CONDITIONS
Official Title
The Effects of Augmented Reality Versus Virtual Reality
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of hemiplegia (ICD-10 code G81)
- Age 18 years or older
- Ability to walk with or without assistance (Functional Ambulation Classification score of 2 or higher)
You will not qualify if you...
- Incomplete completion of the assessment form
- Refusal to participate in the study
- Aphasia
- Montreal Cognitive Assessment score below 10
- Presence of extra neurological or orthopedic problems unrelated to stroke
- Recurrent stroke
- Modified Ashworth Scale (MAS) score of 3-4 in the lower extremities
- Desire to withdraw from the study
- Inability to adapt to the technological devices used in the study (e.g., visual or hearing impairments)
- Missing three consecutive treatment sessions
- Botulinum toxin-A injection to the lower extremity during treatment or within the last 6 months
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Ankara Bilkent City Hospital
Ankara, Çankaya, Turkey (Türkiye), 06800
Actively Recruiting
Research Team
M
Murat Akıncı, Msc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
3
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