Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07113093

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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)
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Ankara Bilkent City Hospital

Ankara, Çankaya, Turkey (Türkiye), 06800

Actively Recruiting

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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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