- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06076148
Virtual Reality and Technologies for Elderly
July 10, 2025 updated by: TOPMED
Aging Well by Being Connected - Phase 1
The objective of this clinical trial is to understand the determinants and opportunities for acceptance of immersive technologies to support physical, cognitive, and social health and the possibilities for "aging well" among the new generation of older adults. The main questions it aims to answer are:
- What are the needs and expectations in terms of immersive activities and intervention methods according to age?
- Do different game modes influence the needs and expectations in immersive activities of this population? 50 participants will be asked to complete a preliminary questionnaire about their activity habits and preferences. They will then be invited to participate in individual or multiplayer virtual reality game trials, a post-trial discussion about their experience and a questionnaire completion.
Study Overview
Study Type
Interventional
Enrollment (Actual)
7
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
-
-
-
Quebec, Canada, G1S1C1
- Topmed
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Be 50 years old or older
Exclusion Criteria:
- Having functional limitations
- Having cognitive impairments
- Being at risk of epilepsy
- Not being autonomus
- Having a pacemaker
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: Supportive Care
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Individual then multiplayer games
Participants of this group will conduct the sessions in the following order : Focus group about individual virtual reality games then Focus group about multiplayer virtual reality games.
|
three individual games (physical, cognitive and relaxation) and two multiplayer games will be tested.
|
|
Experimental: Multiplayer then individual games
Participants of this group will conduct the sessions in the following order : Focus group about multiplayer virtual reality games then Focus group about individual virtual reality games.
|
three individual games (physical, cognitive and relaxation) and two multiplayer games will be tested.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perception of Immersive Technologies Experience
Time Frame: Immediately after each intervention (Week 1, Week 2)
|
4 open questions were asked during the focus group about satisfaction with the trials.
The answers were assessed through a qualitative data theme analysis.
The total number of mentionned items by the intervention group is reported for two themes: appreciated items(things that the participants liked during the games), less appreciated items (things that the participants didn't like during the games).
|
Immediately after each intervention (Week 1, Week 2)
|
|
Integration of Virtual Reality
Time Frame: Immediately after each intervention (Week 1, Week 2)
|
3 open questions were asked during the focus group about intergration of virtual reality(VR) in the daily lives of the participants.
The answers were assessed through a qualitative data theme analysis.
The total number of mentionned items by the intervention group is reported for two themes: obstacles(factors that make the integration of VR harder in the participant's life), facilitating factors(factors that make the integration of VR easier in the participant's life), .
|
Immediately after each intervention (Week 1, Week 2)
|
|
Acceptability of Immersive Technologies
Time Frame: Immediately after each intervention (Week 1, Week 2)
|
1 open question was asked during the focus group about intention to use virtual reality(VR) in the daily lives of the participants.
The answers were assessed through a qualitative data theme analysis.
The total number of mentionned items by the intervention group is reported for one theme: use case of VR items(ways of using VR in the participants daily lives).
|
Immediately after each intervention (Week 1, Week 2)
|
|
Change From Baseline in Interest in Immersive Activities
Time Frame: Baseline and immediately after each intervention (Week 1, Week 2)
|
Change from baseline in total score for 13 questions with 3 point scale (low, medium, high respectively scored 1,2,3).
Minimum=13(low interest); Maximum=39(High interest);
|
Baseline and immediately after each intervention (Week 1, Week 2)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in interest in immersive activities
Time Frame: Baseline and immediately after the intervention
|
Total score for 13 questions with 3 point scale (low, medium, high respectively scored 1,2,3)
|
Baseline and immediately after the intervention
|
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)
April 14, 2023
Primary Completion (Actual)
February 9, 2024
Study Completion (Actual)
February 9, 2024
Study Registration Dates
First Submitted
March 6, 2023
First Submitted That Met QC Criteria
October 6, 2023
First Posted (Actual)
October 10, 2023
Study Record Updates
Last Update Posted (Actual)
July 29, 2025
Last Update Submitted That Met QC Criteria
July 10, 2025
Last Verified
July 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- RD-407_VR 50+
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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