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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.
Full 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.
Enrollment
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Volunteers
Inclusion criteria
People hospitalized in the SMR unit at La Porte Verte Hospital for a minimum of 3 weeks,
Exclusion criteria
People under guardianship or curatorship,
Primary purpose
Allocation
Interventional model
Masking
50 participants in 2 patient groups
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Central trial contact
Fatima Zohra IZEDAREN; Baptiste ISABET
Data sourced from clinicaltrials.gov
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