RECRUITING

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

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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

Official Title

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

Quick Facts

Study Start:2023-11-01
Study Completion:2024-08
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05868369

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients 18 years of age or older with hip pathology
  2. * Failed non-operative treatment of hip pathology
  3. * Undergoing primary, elective and isolated hip arthroscopy for their hip pathology
  4. * Complete pre-operative and post-operative questionnaires
  1. * Minors (17 years of age and younger)
  2. * Traumatic injuries undergoing emergent surgery
  3. * Undergoing revision hip arthroscopic surgery
  4. * Do not complete pre-operative and post-operative questionnaires
  5. * Patients not able to undergo elective surgery
  6. * Pregnant women
  7. * Prisoners
  8. * Patients with conditions that interfere with VR usage including: history of seizure or epilepsy, facial injury precluding safe placement of headset, visual impairment impacting ability to visualize VR images, hearing impairment impacting ability to follow audio instructions

Contacts and Locations

Study Contact

Brooke Bergeron, ATC
CONTACT
(412) 849-9462
brooke.bergeron@cskerlanjobe.org
Jasmine galloway, BS
CONTACT
(412) 849-9462
jasmine.galloway@cskerlanjobe.org

Principal Investigator

Karen Ladnier, MS
STUDY_DIRECTOR
Cedar -Sinai Kerlan jobe orthopedic institute

Study Locations (Sites)

Kerlan Jobe
Los Angeles, California, 90045
United States
Kerlan Jobe
Los Angeles, California, 90045
United States

Collaborators and Investigators

Sponsor: Cedars-Sinai Medical Center

  • Karen Ladnier, MS, STUDY_DIRECTOR, Cedar -Sinai Kerlan jobe orthopedic institute

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-11-01
Study Completion Date2024-08

Study Record Updates

Study Start Date2023-11-01
Study Completion Date2024-08

Terms related to this study

Keywords Provided by Researchers

  • virtual reality

Additional Relevant MeSH Terms

  • Hip Pain Chronic