- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05582863
Effects of a 12-week VR Intervention on the Functional Fitness of Adults of Different Age Ranges
Effects of a 12-week Virtual Reality-based Fitness Intervention on the Functional Fitness of Adults of Different Age Ranges
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Taipei, Taiwan, 106
- NTNU
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- aged more 65 and less 84 years
- with no listening/vision impairments
- who did not have any history of illness based on their response to the Physical Activity Readiness Questionnaire (PAR-Q)
- interested in the virtual reality exercise
Exclusion Criteria:
- age less than 65 or more than 84 years
- disability and unable to live independently
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention group.
The experimental group attended a VR exercise routine twice a week for 12 weeks. Device:1 computer virtual reality online software and 3 large projectors were used to project videos on the wall in a wrap-around state. |
The experimental group performed a 75-90-minute VR exercise routine twice a week for 12 weeks.
|
|
No Intervention: Control group.
Participants in the control group received no intervention and had normal daily activites.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Senior Fitness Test
Time Frame: Senior Functional fitness to specify a period "change" is being assessed. The time points for assessment were week 1 (pre-test), and 12 (post-test).
|
The Senior Fitness Test was used to assess the functional fitness of the participants. The test has six items and evaluations of four physical functional dimensions using the following movements: Back scratch was assessed for upper body flexibility (units of measurement: cm). Chair sit-and-reach movement evaluates lower body flexibility (cm). Arm curl movement assesses upper body strength (times). Chair-stand test evaluates lower body muscle strength (times). 2-minute step exercise evaluates cardiorespiratory fitness (times). 8-foot up-and-go evaluates balance and agility, (sec). The back scratch, chair-and-reach, arm curl, chair stand, and 2-minute step of higher scores mean better functional fitness. The 8-foot up-and-go of higher scores means poorer functional fitness. The study measures the change in functional fitness of older adults from a 1-week baseline to 12 weeks (i.e., exercise intervention phase). |
Senior Functional fitness to specify a period "change" is being assessed. The time points for assessment were week 1 (pre-test), and 12 (post-test).
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Weight and Kilograms test
Time Frame: Not assessing change.The test was only a one-time measure at week 1(pre-test).
|
Measure older adults of height by attaching cloth ruler tape to the wall (e.g., height in centimeters). The weight of the elderly is measured using commercially available electronic weighing machines. (e.g., weight in kilograms). The height and weight measurements of older people are aggregated to produce a reported value (e.g., weight and height will be combined to report BMI in kg/m2). |
Not assessing change.The test was only a one-time measure at week 1(pre-test).
|
Collaborators and Investigators
Investigators
- Study Director: Lee Szu-Hsien, Research Ethics Committee, National Taiwan University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- litingwang_1
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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