Study Results
Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.
View full resultsBasic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
7 participants
INTERVENTIONAL
2023-04-14
2024-02-09
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
* 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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Contribution of Virtual Reality to the Well-being of Elderly Patients Hospitalized in SMR
NCT06985732
Virtual Reality and Occupational Performance, Satisfaction, and Quality of Life of Older Adults
NCT03784053
Effects of Immersive Virtual Reality on Physical Function, Fall-Related Outcomes, Fatigue, and Quality of Life in Older Adults
NCT07007026
Seniors' Intraoperative Management Under Locoregional Anesthesia Integrating Virtual Reality
NCT06515873
Comparison of the Benefits of a Personalized Intervention (Virtual Environment and Device) Compared to Usual Care
NCT05759026
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
CROSSOVER
SUPPORTIVE_CARE
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
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.
Virtual reality games
three individual games (physical, cognitive and relaxation) and two multiplayer games will be tested.
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.
Virtual reality games
three individual games (physical, cognitive and relaxation) and two multiplayer games will be tested.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Virtual reality games
three individual games (physical, cognitive and relaxation) and two multiplayer games will be tested.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Having cognitive impairments
* Being at risk of epilepsy
* Not being autonomus
* Having a pacemaker
50 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Natural Sciences and Engineering Research Council, Canada
OTHER
SEC Fonds Immobilier Groupe Maurice
UNKNOWN
Fédération Québécoise des Loisirs en Institution
UNKNOWN
Fédération de l'Age D'Or du Québec
UNKNOWN
TOPMED
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
TOPMED
Québec, Quebec, Canada
Countries
Review the countries where the study has at least one active or historical site.
Provided Documents
Download supplemental materials such as informed consent forms, study protocols, or participant manuals.
Document Type: Study Protocol
Document Type: Informed Consent Form
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
RD-407_VR 50+
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.