Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Anxiety Disorders
  • Residents of Retirement Home (EHPAD)
Type
Interventional
Phase
Not Applicable
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Supportive Care

Participation Requirements

Age
Between 75 years and 125 years
Gender
Both males and females

Description

The purpose of this muliticentric, interventional, uncontrolled study is to assess the tolerance of the virtual environment in the elderly living in a nursing home subjects who fulfil the inclusion criteria and after signing the informed consent will benefit from three individual virtual reality (VR...

The purpose of this muliticentric, interventional, uncontrolled study is to assess the tolerance of the virtual environment in the elderly living in a nursing home subjects who fulfil the inclusion criteria and after signing the informed consent will benefit from three individual virtual reality (VR) sessions. The sessions will be performed out with one day apart An assessment of anxiety trait and well-being of each subject will be performed before the first session (D1) and after the third (D3). An assessment of anxiety as a condition will be performed before and after each session. Heart rate and blood pressure measurements will be made before, during and after each session. At the end of each session, an evaluation of cybersickness will be performed. Feedback on the acceptability of the experience will be provided at the end of each session. Each session will last 1 hour in total: the person will visualize a single scene of virtual reality presenting a natural environment of a duration of 7 minutes preceded by a time of introduction, evaluation and followed by a time dedicated to evaluations and maintenance.

Tracking Information

NCT #
NCT04365829
Collaborators
Not Provided
Investigators
Study Chair: Emmanuelle DURON, MD Geriatric Department, Paul Brousse Hospital