Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Single 2‑hour Empowered Relief class versus usual care to reduce postoperative pain after elective orthopedic surgery

Official title: Comparison of the Efficacy of an Empowered Relief Single-Session Versus Standard Care for Reducing Postoperative Pain Following Elective Orthopedic Surgery: A Randomized Controlled Trial

Run by Université de Sherbrooke · NCT07392099 · Data updated 2026-11-12

This trial tests whether a single 2-hour Empowered Relief pain-management class can help French-speaking adults with chronic pain after elective orthopedic surgery have less postoperative pain and better recovery than standard care over 6 weeks and 3 months.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment134 (estimated)
SponsorUniversité de Sherbrooke
Academic / other
Locations1 site (Sherbrooke, Quebec)
StatusRecruiting
StartedMay 5, 2025
Main results expectedSeptember 2026
Study endsSeptember 2027
Registry record updatedFebruary 6, 2026
Trial IDNCT07392099 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 and older who speak French, have chronic pain related to their surgical indication of greater than 4/10 for more than 3 months, and can attend and complete the single-session class are ideal candidates.

Probably not a fit

Patients with cancer-related pain, significant cognitive impairment, non‑French speakers, or those who previously completed Empowered Relief are unlikely to benefit from this particular intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized, pragmatic trial compares a single-session, 2-hour group Empowered Relief (ER) class based on CBT principles to usual postoperative care following elective orthopedic surgery. Participants are French-speaking adults with chronic pain (>4/10 for >3 months) who are randomized to receive ER plus usual care or usual care alone. Outcomes include postoperative pain and recovery measures collected at 6-week and 3-month follow-ups, along with acceptability of the ER intervention. The trial is conducted at CIUSSSE de l'Estrie CHUS (Sherbrooke, Quebec) using the French-Canadian version of ER.

Why it matters

Potential benefit: If successful, this could provide patients with a low-cost, easy-to-deliver 2-hour class that reduces postoperative pain and improves recovery after elective orthopedic surgery.

How similar studies have gone: Single-session Empowered Relief and other brief CBT-based interventions have shown benefit in some chronic pain settings, but evidence specifically for postoperative orthopedic populations is still limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Pain \>4/10 for \>3 months related to the surgical indication
* French fluency
* Ability to adhere to and complete study protocol
* Males and females, 18+

Exclusion Criteria:

* Participated in another project that may cause bias in the study results
* Pain related to cancer
* Cognitive impairment, non-French speaking, or factors that would preclude comprehension of material or full participation in ER
* Previous participation in ER

Where it's running

  • CIUSSSE de l'Estrie CHUS
    Sherbrooke, Quebec, Canada
    Recruiting

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.