Clinical Trials Directory

Trials / Completed

CompletedNCT04892940

Use of Virtual Reality to Reduce Morphine Consumption in Adolescents Undergoing Scoliosis Surgery

Use of Virtual Reality to Reduce Morphine Consumption in Adolescents Undergoing Scoliosis Surgery: a Prospective Randomized Open-label Study. Virtual Reality for Analgesia in Spine Surgery

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
101 (actual)
Sponsor
University Hospital, Toulouse · Academic / Other
Sex
All
Age
13 Years – 18 Years
Healthy volunteers
Not accepted

Summary

The objective is to evaluate the effect of the association of virtual reality sessions with usual management on the cumulative consumption of morphine equivalent post-operatively in adolescents aged 13 to 18 years who have undergone scoliosis surgery.

Conditions

Interventions

TypeNameDescription
DEVICEVirtual Reality (VR) techniqueThe "PICO G2 4k" helmet from the Chinese manufacturer Pico which is an autonomous virtual reality helmet will be used. The sessions proposed last 20 minutes with a "child pain" protocol. The teenager will be able to choose his universe (forest, beach, mountain, aquatic, space), the voice that accompanies him (man, woman, none), the sound environment of music therapy (6 to choose from). Each patient in the experimental group benefits from a virtual reality program including two daily sessions during their stay in the continuing care unit from the first post-operative day until the third post-operative day. Each session is proposed by a nurse anesthetist from the pain team and trained in the proper use of the equipment.This virtual reality program will be added to the standard analgesic protocol for the experimental group.
DRUGAnalgesic protocolPatients randomized in the "control" group receive the usual analgesic protocol of the department postoperatively.

Timeline

Start date
2022-02-21
Primary completion
2024-07-24
Completion
2024-07-24
First posted
2021-05-19
Last updated
2025-01-23

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04892940. Inclusion in this directory is not an endorsement.