Actively Recruiting
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
Led by Université de Sherbrooke · Updated on 2026-02-06
134
Participants Needed
1
Research Sites
121 weeks
Total Duration
On this page
Sponsors
U
Université de Sherbrooke
Lead Sponsor
E
Estrie University Integrated Health and Social Services Center - University Hospital of Sherbrooke
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study is to evaluate the efficacy and acceptability of the French-Canadian version of ER compared to standard care in reducing postoperative pain and improving recovery outcomes at 6-week and 3-month follow-ups after elective orthopedic surgery.
CONDITIONS
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
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pain greater than 4 out of 10 for more than 3 months related to the surgical reason
- Fluent in French
- Able to follow and complete the study procedures
- Male or female aged 18 years or older
You will not qualify if you...
- Participation in another study that could bias results
- Pain caused by cancer
- Cognitive problems or inability to understand French or fully participate in the Empowered Relief session
- Previous participation in the Empowered Relief program
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CIUSSSE de l'Estrie CHUS
Sherbrooke, Quebec, Canada, J1H 5N4
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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