PRT for Chronic Low Back Pain

What this study is about

The goal of this clinical trial is to learn whether Pain Reprocessing Therapy (PRT) is a feasible and acceptable treatment to complete for working-age adults (ages 18-65) with chronic low back pain. The main questions it aims to answer are: Is PRT acceptable and feasible for people with chronic low back pain to complete? Does PRT help reduce pain intensity and interference, while improving functional outcomes in people with chronic low back pain? Researchers will compare PRT to a Monitoring and Education Program to see whether participants who receive PRT experience greater improvements in pain, daily functioning, and well-being. Participants will: * Be randomly assigned to the PRT group or the Monitoring and Education group * Participate in 8 intervention sessions over an 8-week period * Wear an activity monitor for 8 weeks * Attend a follow-up assessment after completing the intervention and another assessment 3 months later

Who can join (things the study team will check)

✅ You may be able to join if…

• Working age adults (18-65)
• Male or Female at birth
• Persisting back pain for at least 3 months occurring at least half of the days in the past 6 months
• Pain score of at least 4/10 (on a 10-point rating scale)
• Ability to speak and understand English in order to follow study procedures and engage in study interventions.

🚫 You may not be able to join if…

• Compensation seeking claim/litigation/WSIB claim
• Severe active psychiatric disorders (e.g., psychosis, substance use disorder)
• An active medical issue such as untreated inflammatory disorder (e.g. ankylosing spondylitis, psoriatic arthritis)
• Active cancers affecting the spine or body
• Unexplained unintended weight loss of 20 lbs. or more in the past year
• Inability to control bowel or bladder, function
• Individuals who have received or are currently receiving one-on-one or group psychotherapy for chronic low back pain within the past 2 years (e.g., mindfulness, meditation, cognitive behavioural therapy, acceptance and commitment therapy, pain reprocessing therapy, or emotional awareness and exposure therapy).
• Logistical or technical barriers (e.g. transportation challenges, scheduling constraints, or difficulty using fitness trackers

Where this trial is running

• Toronto Rehabilitation Institute - University Centre, Toronto, Ontario, Canada

Who to contact

Mariam Hasan · +1 416-597-3422 · Mariam.hasan@uhn.ca

It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT07696741.