- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03834545
Improved Motivation for Physical Activity in an Institutionalized Geriatric Population Through a Virtual Environment (Cyclepad Pilot)
Improvement of Motivation for Physical Activity in an Institutionalized Geriatric Population Thanks to a Virtual Environment: Comparison of Motivation Between Classic Bike and Bike With Virtual Environment
Study Overview
Status
Conditions
Detailed Description
The World Health Organization (WHO) recommends for people aged 65 years and over a weekly practice of at least 150 minutes of moderate-intensity endurance activities or at least 75 minutes of activity. endurance of sustained intensity, or an equivalent combination of moderate and sustained activity. However, the attractiveness for physical activity fades over the years limiting the practice of physical activity. Several types of unconventional approaches have already shown their effectiveness in the prevention of falls in the elderly but these practices find their limits in the lack of adherence to this type of exercise, especially in nursing homes. New virtual reality and gaming technologies have recently emerged and are being used as tools to prevent the risk of falling. The use of these new tools has advantages over conventional exercises: motivating.
The investigators aimed to test the interest of a virtual environment with cycling to increase the motivation of physical activity practice in institutionalized older adults.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Normandy
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Caen, Normandy, France, 14000
- CAEN University Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- age over 65
- ability to cycle
Exclusion Criteria:
- unstable cardiopathy
- New York Heart Association classification III or IV
- severe cognitive disorders with inability to follow simple orders (follow investigator, ride on the ergometric bicycles, pedal)
- visual disturbance preventing counting fingers at 5m
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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cycling group
They attended three sessions of exercise on three different conditions : a classic ergometric bicycle without chairback, an ergometric bicycle with chairback with virtual environment and the other session without virtual environment
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Cycling distance in meters
Time Frame: 3 months
|
Primary outcome was the cycling distance measured at each session without encouragement
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3 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Time spent pedaling in seconds per session
Time Frame: 3 months
|
Measure of the time spent pedaling per session without encouragement
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3 months
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The average speed in meters per second per session
Time Frame: 3 months
|
Measure of the average cycling speed per session without encouragement.
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3 months
|
Mean pedaling cadence per session in revolutions per minute
Time Frame: 3 months
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Measure of the average pedaling cadence per session without encouragement.
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3 months
|
Borg rating of perceived exertion scale
Time Frame: 3 months
|
Measure of the perceived exertion after each cycling session with Borg rating of perceived exertion scale.
Range 0-10.
Ten corresponding to the maximal perceived exertion
|
3 months
|
Mean pedaling power per session in Watts
Time Frame: 3 months
|
Measure of the pedaling power per session without encouragement
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3 months
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Closed-ended question to know which condition they would prefer for a futur exercise session.
Time Frame: 3 months
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Participant were asked at the end of the third session, which condition they would prefer for a futur exercice session.
Possible answers: "Classic ergometric bicycle Kettler E3)", "Cycleo without virtual environment", "Cycleo with virtual environment", "None".
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3 months
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Collaborators and Investigators
Sponsor
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
Other Study ID Numbers
- ARUET
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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