- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04284709
Exergaming for Community-Dwelling Older Adults
February 23, 2020 updated by: CY Song, National Taipei University of Nursing and Health Sciences
Novel Mat Exergaming to Improve the Physical Performance, Cognitive Function, and Dual-task Walking and Decrease the Fall Risk of Community-dwelling Older Adults
This study aimed to utilize an interactive exergame mat system to develop a novel cognitive-physical training program and explore the training effects on physical performance, cognitive function, dual-task walking (DTW), and fall risk compared to the control condition.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
The exercise group performed exergames with simultaneous cognitive-physical training, while the control group underwent a multicomponent exercise intervention focused on physical and cognitive training.
A 2-hour training session was completed weekly for 3 months.
Study Type
Interventional
Enrollment (Actual)
110
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Taipei, Taiwan, 11219
- National Taipei University of Nursing and Health Sciences
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
65 years and older (Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- aged 65 years or older, and being able to walk independently without any assistive devices
Exclusion Criteria:
- had severe lower-extremity joint pain, cognitive impairment, or visual problems that impeded their participation
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: exercise group
exergames with simultaneous cognitive-physical training
|
combined physical and cognitive training
|
|
Active Comparator: control group
multicomponent exercise intervention focused on physical and cognitive training
|
combined physical and cognitive training
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
change in lower-limb muscle strength
Time Frame: before and after 3-month exercise training interventions
|
30-second chair stand test
|
before and after 3-month exercise training interventions
|
|
change in upper-limb muscle strength
Time Frame: before and after 3-month exercise training interventions
|
30-second arm curl test
|
before and after 3-month exercise training interventions
|
|
change in aerobic endurance
Time Frame: before and after 3-month exercise training interventions
|
2-minute step test
|
before and after 3-month exercise training interventions
|
|
change in lower-body flexibility
Time Frame: before and after 3-month exercise training interventions
|
chair sit and reach test
|
before and after 3-month exercise training interventions
|
|
change in upper-body flexibility
Time Frame: before and after 3-month exercise training interventions
|
back scratch test
|
before and after 3-month exercise training interventions
|
|
change in dynamic balance
Time Frame: before and after 3-month exercise training interventions
|
8-foot up and go test
|
before and after 3-month exercise training interventions
|
|
change in static balance
Time Frame: before and after 3-month exercise training interventions
|
single-leg stand test
|
before and after 3-month exercise training interventions
|
|
change in grasp strength
Time Frame: before and after 3-month exercise training interventions
|
hand grip strength
|
before and after 3-month exercise training interventions
|
|
change in lower limb motor function
Time Frame: before and after 3-month exercise training interventions
|
foot tapping test
|
before and after 3-month exercise training interventions
|
|
change in cognitive function
Time Frame: before and after 3-month exercise training interventions
|
Montreal Cognitive Assessment
|
before and after 3-month exercise training interventions
|
|
change in cognitive dual-task walking
Time Frame: before and after 3-month exercise training interventions
|
8-foot up and go walking while counting
|
before and after 3-month exercise training interventions
|
|
change in motor dual-task walking
Time Frame: before and after 3-month exercise training interventions
|
8-foot up and go walking while carrying a tray
|
before and after 3-month exercise training interventions
|
|
change in fall risk
Time Frame: before and after 3-month exercise training interventions
|
fall risk questionnaire
|
before and after 3-month exercise training interventions
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 14, 2018
Primary Completion (Actual)
April 30, 2019
Study Completion (Actual)
April 30, 2019
Study Registration Dates
First Submitted
February 20, 2020
First Submitted That Met QC Criteria
February 23, 2020
First Posted (Actual)
February 26, 2020
Study Record Updates
Last Update Posted (Actual)
February 26, 2020
Last Update Submitted That Met QC Criteria
February 23, 2020
Last Verified
February 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- 18-116-B
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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