Virtual Reality on Patient Satisfaction in Ambulatory Orthopedic Surgery

Not Applicable

Not yet recruiting

• Conditions: Orthopedic
• Interventions: Device: Virtual reality

• Registration Number: NCT04905355
• Lead Sponsor: GCS Ramsay Santé pour l'Enseignement et la Recherche

Brief Summary

Few studies were interested in the patient satisfaction after ambulatory surgery. Most of them showed negative results due to psychological factors. The intervention including surgery and hospitalization is still perceived as painful memory for most of patients. Several improving axes have been explored to change global patient experience. One new idea could be to offer a virtual reality experience during the surgery or local regional anesthesia. Some studies showed that immersive experience can reduce the anxiety, the pain, improve the patient comfort and recovery after surgery. The virtual reality is commonly used but it has to be evaluated in terms of efficiency with a prospective study and objective outcomes to go further in the improvement of the experience and the care offer to patients.

Detailed Description

The study is to compare the patient satisfaction between patients with virtual reality experience and patients without VR experience during the ambulatory orthopedic surgery under local regional anesthesia.

Study Timeline

• Study First Submitted: 2021-05-24
• Study First Submitted QC: 2021-05-24
• Study First Posted: 2021-05-27
• Status Verified: 2024-04
• Last Update Submitted: 2024-04-17
• Last Update Posted: 2024-04-18
• Study Start: 2024-09-01
• Primary Completion: 2026-08-31
• Study Completion: 2026-08-31

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 388

Inclusion Criteria

• Participant who has an ambulatory orthopedic surgery under local regional anesthesia, planned or performed in emergency
• Participant who has been given appropriate information about the study objectives and who has given his/her express written and informed consent prior to conduct any study-related procedures.

Exclusion Criteria

• Participant with visual deficiency or deaf
• Participant who can bear virtual reality
• Participant whose physical and / or psychological health is severely impaired, which according to the investigator may affect the participant's compliance with the study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Virtual Reality (VR)	Virtual reality	Patient with VR experience during the ambulatory orthopedic surgery

Primary Outcome Measures

Name	Time	Method
Patient satisfaction of operating room management by Net Promoter Score	One Day after surgery	Net Promoter Score (scale from 0 to 10 with 3 groups: promoters for 9-10, passive for 7-8 and detractor for below 6)

Secondary Outcome Measures

Name	Time	Method
Patient satisfaction of ambulatory hospitalization by e-SATIS questionnaire	One Day after surgery	e-SATIS questionnaire : measure of hospitalization experience and patient satisfaction (the best scoring is 100 , excellent satisfaction)

Trial Locations

Locations (1)

RGDS-Clinique Aguiléra; 🇫🇷 Biarritz, France