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Clinical Trials/NCT04905355
NCT04905355
Not yet recruiting
Not Applicable

Contribution of Virtual Reality on Patient Satisfaction in Ambulatory Orthopedic Surgery

GCS Ramsay Santé pour l'Enseignement et la Recherche1 site in 1 country388 target enrollmentSeptember 1, 2024
ConditionsOrthopedic

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Orthopedic
Sponsor
GCS Ramsay Santé pour l'Enseignement et la Recherche
Enrollment
388
Locations
1
Primary Endpoint
Patient satisfaction of operating room management by Net Promoter Score
Status
Not yet recruiting
Last Updated
2 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
September 1, 2024
End Date
August 31, 2026
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
GCS Ramsay Santé pour l'Enseignement et la Recherche
Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Patient satisfaction of operating room management by Net Promoter Score

Time Frame: 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 Outcomes

  • Patient satisfaction of ambulatory hospitalization by e-SATIS questionnaire(One Day after surgery)

Study Sites (1)

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