Contribution of Virtual Reality to the Well-being of Elderly Patients Hospitalized in SMR

NCT ID: NCT06985732

Last Updated: 2025-05-28

Study Results

Results pending

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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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-09-01

Study Completion Date

2026-09-01

Brief Summary

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The objective of this clinical trial is to evaluate the effect of using virtual reality on the well-being of elderly patients hospitalized in SMR for 3 weeks. The study also allows to evaluate the effect of VR on apathy, and the autonomy of patients hospitalized in the SMR department for 3 weeks.

Detailed Description

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Patients meeting the inclusion criteria and agreeing to participate in the study will be enrolled and then randomized to either the VR immersion group or the control group. Patients included in the protocol will not undergo any changes to their care. Patients in the experimental group will receive 12 virtual reality sessions in addition to their usual care.

Conditions

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Virtual Reality

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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VR group

Group Type EXPERIMENTAL

Virtual Reality

Intervention Type OTHER

Use of virtual reality to elicit positive emotions and improve the well-being of elderly patients hospitalized in SMR

contrrol arm

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Virtual Reality

Use of virtual reality to elicit positive emotions and improve the well-being of elderly patients hospitalized in SMR

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

People hospitalized in the SMR unit at La Porte Verte Hospital for a minimum of 3 weeks,

* People with preserved or slightly impaired cognitive status with an MMSE ≥ 20,
* People who have been informed and have signed written informed consent

Exclusion Criteria

People under guardianship or curatorship,

* People with difficulty understanding the VR study and materials,
* People with vision problems that impact the use of VR,
* People with hearing problems that impact the use of VR,
* People with epilepsy,
* People at risk of nausea and dizziness when using the VR headset,
* People who cannot tolerate the VR headset,
* Not affiliated with a social security scheme.
* People receiving care with reflexology and relaxation massage
Minimum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Médical Porte Verte

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Central Contacts

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Baptiste ISABET

Role: CONTACT

0634227138 ext. 0033

Fatima Zohra IZEDAREN

Role: CONTACT

Other Identifiers

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2025-A00983-46

Identifier Type: -

Identifier Source: org_study_id

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