Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
40 participants
INTERVENTIONAL
2024-05-01
2024-10-23
Brief Summary
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Thee investigator hypothesize (1) that a VR headset-based intervention based on listening to and observing a concert of musicians playing classical music is feasible for patients hospitalized at the IUGM's URFI and in patients attending the geriatric outpatient clinic, and (2) that this intervention can improve their mental health - i.e. their positive emotions, well-being and quality of life - and reduce their anxiety.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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Intervention
participants will listen to and watch a concert of musicians playing classical music through a VR headset
VR
The participant will be seated comfortably in an armchair. The intervention will last 15 minutes. It will take place once.
This group's intervention will be to watch and listen with VR headphones to a concert by a group of musicians playing music.
Control
participants will simply listen to the concert through headphones
Music only
The participant will be seated comfortably in an armchair. The intervention will last 15 minutes. It will take place once.
This group's intervention will be to listen with conventional headphones to a concert by a group of musicians playing music.
Interventions
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VR
The participant will be seated comfortably in an armchair. The intervention will last 15 minutes. It will take place once.
This group's intervention will be to watch and listen with VR headphones to a concert by a group of musicians playing music.
Music only
The participant will be seated comfortably in an armchair. The intervention will last 15 minutes. It will take place once.
This group's intervention will be to listen with conventional headphones to a concert by a group of musicians playing music.
Eligibility Criteria
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Inclusion Criteria
* be 60 years of age or older,
* not have an acute intercurrent pathology in the week preceding the procedure and during the two days of the procedure,
* have no psycho-behavioural disorders,
* no major neurocognitive disorder at a severe stage,
* no severe visual or hearing impairment,
* no vestibular balance disorders,
* give written consent to participate in the study.
Exclusion Criteria
* Do not understand written or spoken French or English. The participants are French and/or English speakers, and the questionnaires are only available in these 2 languages.
60 Years
ALL
No
Sponsors
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Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal
OTHER_GOV
Responsible Party
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Olivier Beauchet
MD, PhD, director of AgeTeQ Lab at CRIUGM
Locations
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CRIUGM
Montreal, Quebec, Canada
Countries
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Other Identifiers
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2024-2064
Identifier Type: -
Identifier Source: org_study_id
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