Virtual Reality and Genicular Nerve Ablation for Chronic Knee Pain

This study is looking at whether using a virtual reality (VR) headset can help reduce pain during a procedure called cooled genicular nerve radiofrequency ablation (RFA) for chronic knee pain. RFA is a treatment that uses heat to stop nerves from sending pain signals. You might be able to join if you are at least 18 years old, have chronic knee pain (lasting over 6 weeks, average pain score above 4 out of 10), have X-ray evidence of knee osteoarthritis, and have not had knee surgery or RFA on the affected knee before. The study wants to see if VR helps with pain during the procedure, how satisfied patients are, and how their pain and ability to function are one month later. The study is currently unclear about its recruitment status and plans to include 62 participants.

Study design
This study is designed to compare two groups: one group will use a VR headset before and after the RFA procedure, and the other group will receive standard care without VR. It plans to enroll 62 participants.
What's involved
Participants will either wear a VR headset for at least 10 minutes before and 10 minutes after the RFA procedure, or they will receive standard care. Pain will be measured 10 minutes after the procedure, and pain and function will be assessed at 1 month.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for 1 month after the procedure to assess pain and functional outcomes.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06336447

VR and Cooled Genicular Nerve Radio Frequency Ablation for Chronic Knee Pain

Recruiting
NAAges 18+InterventionalTreatment
Northwestern University
~62 participants
Updated 2024-03-28 on ClinicalTrials.gov
What's tested:Experimental: Group #1: Virtual Reality HeadsetGroup 2 No Virtual Reality Headset

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Procedural related pain
Measured over 10 minutes after procedure
Pain, Chronic
1 sites across 1 states
Illinois1
  • Jason Ross, MD · PRINCIPAL_INVESTIGATOR · Northwestern Univesity

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Eligibility criteria

Inclusion

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

Exclusion

Individuals who do not have evidence of osteoarthritis on X-ray,
Secondary gain expected to influence treatment outcomes
Poorly controlled psychiatric condition that could affect outcome (e.g. active substance abuse) or impose a barrier to participation
Chronic opioid use and anticoagulation therapy that cannot be stopped and could warrant a different treatment approach (e.g. phenol ablation)
Severe motion sickness
Seizure disorder
Vision loss
Pregnant
Nursing
  • Procedural related pain10 minutes after procedure

    Reported procedural related pain on a 0-10 verbal rating scale (VRS)