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

Not Applicable

Not yet recruiting

• Conditions: Virtual Reality

• Registration Number: NCT06985732
• Lead Sponsor: Centre Médical Porte Verte

Brief Summary

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

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.

Study Timeline

• Status Verified: 2025-05
• Study First Submitted: 2025-05-14
• Study First Submitted QC: 2025-05-21
• Study First Posted: 2025-05-22
• Last Update Submitted: 2025-05-22
• Last Update Posted: 2025-05-28
• Study Start: 2025-09-01
• Primary Completion: 2026-03-01
• Study Completion: 2026-09-01

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 50

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
WHO-5	4 times throughout of study at baseline and after each VR session	measure well-being. The score is between 0-100 a high score means better wellness