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Standard regimen +iVR Group for Hip Pain

N/A

Recruiting

Research Sponsored by Cedars-Sinai Medical Center

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be older than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up one time at day 1 post operative

Awards & highlights

Study Summary

This trial studies if using virtual reality (VR) in post-op care can reduce post-op pain, compared to opioids & local blocks. It'll enroll adults of all ages undergoing hip arthroscopy.

Who is the study for?

This trial is for adults of any age who have hip pain due to a condition that hasn't improved with non-surgical treatments. They must be scheduled for their first elective hip arthroscopy and willing to complete questionnaires before and after the surgery.Check my eligibility

What is being tested?

The study is testing if using immersive virtual reality (iVR) after hip surgery can better manage pain compared to standard methods like opioids and local anesthesia. Participants will use a head-mounted iVR device in the post-anesthesia care unit.See study design

What are the potential side effects?

While not explicitly stated, potential side effects may include discomfort or dizziness from iVR, typical surgical recovery pains, and common side effects from standard pain medications such as nausea or constipation.

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ one time at day 1 post operative

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~one time at day 1 post operative

This trial's timeline: 3 weeks for screening, Varies for treatment, and one time at day 1 post operative for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Pain visual analog scale (VAS)

Secondary outcome measures

Anxiety PACU questionnaire

Nausea PACU Questionnaire

Trial Design

2Treatment groups

Experimental Treatment

Active Control

Group I: Standard regimen +iVR GroupExperimental Treatment2 Interventions

postoperative iVR therapy in addition to the standard multimodal pain regimen (including a preoperative local field block

Group II: Standard regimenActive Control1 Intervention

hip arthroscopy patients who receive only the standard regimen (including field block) in the acute postoperative ambulatory setting

Do I qualify?Apply below to find out

Find a Location

Who is running the clinical trial?

Cedars-Sinai Medical CenterLead Sponsor

500 Previous Clinical Trials

164,793 Total Patients Enrolled

Karen Ladnier, MSStudy DirectorCedar -Sinai Kerlan jobe orthopedic institute

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are individuals still being recruited for participation in this experiment?

"The information hosted on clinicaltrials.gov affirms that this medical experiment is currently recruiting participants. It was initially publicized on the 1st of May in 2023 and its most recent update was posted at 10th of May, 2023."

Answered by AI

What is the cap on participant enrollment for this trial?

"Yes, information on clinicaltrials.gov suggests that this experiment is actively hiring patients. The study was first uploaded to the website May 1st 2023 and last updated a week later, with plans to recruit 70 individuals at one trial site."

Answered by AI

Recent research and studies

clinicaltrials.govStudy

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

Michael Banffy, MD 2023. "The Effectiveness of Immersive Virtual Reality as a Pain Control Modality After Hip Arthroscopy". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT05868369.

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