๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-08-03

Pain Reprocessing Therapy in Post-Operative Knee Pain (NCT06800209)

Efficacy and Mechanisms of Pain Reprocessing Therapy in Chronic Post-Operative Knee Pain

๐ŸŸข Recruiting Phase2 ๐Ÿง  Behavioral & Psychological Program Sponsor: Weill Medical College of Cornell University

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

The goal of this clinical trial is to learn whether Pain Reprocessing Therapy (PRT) can help adults with knee pain after knee replacement surgery. The study is comparing PRT to usual care (the regular treatment people get after surgery) to see which works better for relieving pain. The main questions the study aims to answer are: 1. Does PRT help lower pain in people who have chronic knee pain after knee surgery? 2. How do the effects of PRT compare with usual care in terms of pain relief and other factors such as anxiety, depression, and sleep? 3. How does PRT impact the brain? Participants will: 1. Be randomly assigned to receive either PRT or usual care. 2. Complete questionnaires about their pain and health. 3. If in the PRT group, have eight weekly therapy sessions over video calls with a therapist. 4. If interested, may also take part in an optional EEG test to measure brain activity related to pain.

Who can join: Review the eligibility criteria below.

Location: University of Colorado Anschutz Medical Campus โ€” Aurora, Colorado

Age range: 18 Years

๐Ÿงช Interventions in This Study

  • Pain reprocessing therapy (PRT) (BEHAVIORAL)
  • Usual care (OTHER)

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (2 Sites)

  • University of Colorado Anschutz Medical Campus โ€” Aurora, Colorado
  • Hospital for Special Surgery โ€” New York, New York

๐Ÿ“ž Contact the Study Coordinator

Phone: (212) 774-2572

Email: Complexjoint@hss.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Pain, Chronic clinical trials

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—