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Clinical Trials/NCT04166747
NCT04166747
Completed
Not Applicable

Effect of Virtual Reality Based Intervention on Functional Fitness and Quality of Life of Older Population: A Randomized Controlled Trial

Taipei Medical University1 site in 1 country60 target enrollmentOctober 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Aging
Sponsor
Taipei Medical University
Enrollment
60
Locations
1
Primary Endpoint
Measurement of Quality of life
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this study is to assess the influence of virtual reality (VR) on the different parameters, happiness, quality of life and functional fitness, among older population. The study aims to conduct a randomized controlled trial, where the participants in intervention group will use VR and those in control group do not use VR.

Detailed Description

This study aims to conduct a randomized control trial, on 60 older age group participants, and perform the functional fitness test based on the protocol developed by Rikli and Jones, before and after the VR intervention. The functional fitness tests include evaluation of upper body strength, lower body strength, cardiorespiratory endurance, upper body flexibility test, lower body flexibility test, balance, agility test. They will be randomly assigned to the intervention group, receiving the VR program, and the control group who will not receive the VR program. The participants in the intervention group will be asked to use the VR device for 15 minutes, twice a week for 6 weeks, along with their daily routine activities. Control group will carry out the daily routine activities, without the intervention. The change in the quality of life (QOL) and happiness, for both control and intervention groups, will be assessed through EuroQol 5 dimensions 3 level questionnaire (EQ-5D-3L), mini version of Chinese happiness Inventory questionnaire, respectively, to filled at recruitment and follow-up after 6 weeks. The effect of the VR programs will be determined by the comparison of performance, for the functional fitness tests before and after the intervention and also, for the differences between the control and intervention groups

Registry
clinicaltrials.gov
Start Date
October 1, 2019
End Date
March 30, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Shabbir Syed Abdul

Associate Professor

Taipei Medical University

Eligibility Criteria

Inclusion Criteria

  • Participants aged 60 years or older and approach TMU aging center.
  • Able to understand Mandarin Chinese.
  • Gives informed consent to participate
  • No past or current history of serious medical disease
  • Ability to perform activities of daily living
  • Understands the intent of the study

Exclusion Criteria

  • Participants aged below 60 years of age.
  • Not able to understand Mandarin Chinese.
  • Does not gives informed consent to participate
  • Past or current history of serious medical disease
  • Inability to perform activities of daily living
  • Does not understand the intent of the study

Outcomes

Primary Outcomes

Measurement of Quality of life

Time Frame: At enrollment and at 6 weeks after enrollment

Comparison of changes in the quality of life through the questionnaire EQ-5D-3L

Measurement of functional fitness components

Time Frame: At enrollment and at 6 weeks after enrollment

Comparison of changes in the muscle strength through the functional fitness tests.

Measurement of Happiness

Time Frame: At enrollment and at 6 weeks after enrollment

Comparison of changes in the happiness through the questionnaire mini version of Chinese Happiness Inventory.

Study Sites (1)

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