Actively Recruiting

Phase Not Applicable
Age: 55Years - 90Years
All Genders
Healthy Volunteers
NCT06575218

The Effectiveness of Virtual Reality Training Program

Led by Yeditepe University · Updated on 2024-08-30

45

Participants Needed

1

Research Sites

15 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Alzheimer's disease is the most common type of dementia, accounting for 50% of all cases. Advanced age is a significant risk factor for AD. Virtual Reality (VR) is an interactive video game technology that provides computer-generated environments that include physical activity and provide users with experiences similar to those in the real world. VR technology can be used for rehabilitation purposes in individuals with various orthopedic and neurological disorders due to its ability to enhance motor, cognitive learning and neural plasticity (1,2). The aim of our study was to examine the effect of the Virtual Reality Training Program on cognition in individuals with Alzheimer's disease living in the community.

CONDITIONS

Official Title

The Effectiveness of Virtual Reality Training Program

Who Can Participate

Age: 55Years - 90Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 55 years or older
  • Diagnosed with Alzheimer's disease according to DSM-IV criteria by a neurologist
  • Montreal Cognitive Assessment (MOCA) score of 16 or higher
  • Clinical Dementia Rating Scale score less than 2
Not Eligible

You will not qualify if you...

  • Various mobility restrictions or musculoskeletal disorders (e.g., wheelchair use)
  • Clinically significant aphasia preventing understanding of therapist's commands
  • Significant visual or sensory impairment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Ebru Akbuğa Koç

Istanbul, Turkey (Türkiye)

Actively Recruiting

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Research Team

E

Ebru Akbuga Koc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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