The Effectiveness of Immersive Virtual Reality as a Pain Control Modality After Hip Arthroscopy

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug, Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

1. The purpose of the research is to assess the efficacy of postoperative immersive virtual reality (iVR) compared to a standard multimodal pain regimen including opioids and a local block on acute postoperative pain management following hip arthroscopy 2. The primary research procedures are medical record review for demographic information, head-mounted immersive virtual reality experience in PACU, and pre-operative and post-operative surveys 3. The study will enroll adult patients of all ages undergoing elective hip arthroscopy procedures for any diagnosis

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients 18 years of age or older with hip pathology

• Failed non-operative treatment of hip pathology

• Undergoing primary, elective and isolated hip arthroscopy for their hip pathology

• Complete pre-operative and post-operative questionnaires

Locations
United States
California
Kerlan Jobe
RECRUITING
Los Angeles
Kerlan Jobe
RECRUITING
Los Angeles
Contact Information
Primary
Brooke Bergeron, ATC
brooke.bergeron@cskerlanjobe.org
(412) 849-9462
Backup
Jasmine galloway, BS
jasmine.galloway@cskerlanjobe.org
(412) 849-9462
Time Frame
Start Date: 2023-11-01
Estimated Completion Date: 2028-08
Participants
Target number of participants: 70
Treatments
Experimental: Standard regimen +iVR Group
postoperative iVR therapy in addition to the standard multimodal pain regimen (including a preoperative local field block
Active_comparator: Standard regimen
hip arthroscopy patients who receive only the standard regimen (including field block) in the acute postoperative ambulatory setting
Related Therapeutic Areas
Sponsors
Leads: Cedars-Sinai Medical Center

This content was sourced from clinicaltrials.gov