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
Recruiting
N/A
Interventional Study
Chronic Pain
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 134 (estimated)
- Sponsor
- Université de Sherbrooke · Other
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About This Trial
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.
Trial Locations
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Eligibility 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
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Contacts
No contact information available.