Virtual Reality on Patient Satisfaction in Ambulatory Orthopedic Surgery
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Virtual reality.
- Who it may be relevant to
- Registry conditions: Orthopedic. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Contribution of Virtual Reality on Patient Satisfaction in Ambulatory Orthopedic Surgery
Overview
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.
Interventions
- Device Virtual reality
The VR used during the ambulatory orthopedic surgery allows immersive experience in HD-2D virtual environment. Patient can choose among movies, cartoons, entertainments offered for visualization during the surgery
Primary outcome measures
- Patient satisfaction of operating room management by Net Promoter Score [Time frame: One Day after surgery]
Secondary outcome measures (1)
- Patient satisfaction of ambulatory hospitalization by e-SATIS questionnaire [Time frame: One Day after surgery]
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Supportive care
Study locations
France · 1 center
- RGDS-Clinique Aguiléra — Biarritz
Identifiers
NCT: NCT04905355 · 2021-A00479-32