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Can Virtual Reality Improve Patient Tolerance in Patients Undergoing Water Cooled Genicular Nerve Radio Frequency Ablation in Patients With Chronic Knee Pain? A Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study will examine the impact of virtual reality used in conjunction with sedation compared to sedation alone in patients undergoing watervcooled genicular nerve ablations for chronic knee pain. The goals of the study is to determine the relative efficacy of virtual reality as a distraction modality when used as an adjuvant to procedural sedation compared to sedation alone for procedure related pain. To assess procedural satisfaction, and 1-month pain and functional outcomes.To explore whether virtual reality and lower procedure-related pain scores affect 1-month outcomes. And finally to determine whether demographic and clinical characteristics are associated with outcome measures.

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

• Patients undergoing genicular RFA will be eligible for inclusion in the study

• Patients with knee pain, baseline average of \> 4/10

• X-ray evidence of osteoarthritis of the knee

• Pain duration of \>6 weeks and no previous knee surgeries

• Patients will also only be included who have never undergone a RFA on the affected knee

Locations
United States
Illinois
Northwestern Medicine Pain Center
RECRUITING
Chicago
Contact Information
Primary
Paul Fitzgerald, RN,BSN,MS
p-fitzgerald2@northwestern.edu
312-695-1064
Time Frame
Start Date: 2024-01-12
Estimated Completion Date: 2027-02-28
Participants
Target number of participants: 62
Treatments
Experimental: Group #1: Virtual Reality Headset
Group 1 will be assigned to the Virtual Realtity Headset. Participants will wear the headset for at least 10 minutes prior to the planned procedure. Subjects will receive standard procedure. The VR Headset will be removed 10 minutes after the planned procedure.
Active_comparator: Group 2 No Virtual Reality Headset
Group 2 will receive standard care without the use of the Virtuality Reality Headset.
Related Therapeutic Areas
Sponsors
Leads: Northwestern University

This content was sourced from clinicaltrials.gov