World Health Organization site
Skip Navigation Links

Main
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 12 December 2020
Main ID:  NCT03501342
Date of registration: 10/04/2018
Prospective Registration: No
Primary sponsor: Gazi University
Public title: Effects of Immersive Virtual Reality on Balance, Mobility, and Fatigue in Patients With Multiple Sclerosis
Scientific title: Effects of Immersive Virtual Reality on Balance, Mobility, and Fatigue in Patients With Multiple Sclerosis
Date of first enrolment: April 9, 2018
Target sample size: 39
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT03501342
Study type:  Interventional
Study design:  Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: None (Open Label).  
Phase:  N/A
Countries of recruitment
Turkey
Contacts
Name:     Cagla Ozkul
Address: 
Telephone:
Email:
Affiliation:  Gazi University
Key inclusion & exclusion criteria

Inclusion Criteria:

- Participants who are ambulatory and volunteer to participate to the study, in a stable
phase of the disease, without relapses in the last 1 month, with an EDSS between
0-5,5.

Exclusion Criteria:

- Participants who have orthopedic, vision, hearing, or perception problems

- Patients who have any cardiovascular or pulmonary disease in which exercise is
contraindicated



Age minimum: 18 Years
Age maximum: 65 Years
Gender: All
Health Condition(s) or Problem(s) studied
Multiple Sclerosis
Intervention(s)
Other: Virtual reality group
Other: Dynamic Balance Training
Primary Outcome(s)
Berg Balance Scale [Time Frame: Change between baseline and after 8 weeks of intervention will be assessed]
Secondary Outcome(s)
Fatigue Impact Scale [Time Frame: Change between baseline and after 8 weeks of intervention will be assessed]
One-leg standing duration [Time Frame: Change between baseline and after 8 weeks of intervention will be assessed]
Fatigue Severity Scale [Time Frame: Change between baseline and after 8 weeks of intervention will be assessed]
Modified Sensory Organization Test [Time Frame: Change between baseline and after 8 weeks of intervention will be assessed]
Activities-specific Balance Confidence [Time Frame: Change between baseline and after 8 weeks of intervention will be assessed]
Timed Up and Go Test [Time Frame: Change between baseline and after 8 weeks of intervention will be assessed]
Secondary ID(s)
228
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.6 - Version history