Can retraining the brain replace the pill? a big trial tests two non-drug paths to pain relief.
NCT ID NCT03445988
First seen Sep 01, 2026 · Last updated Sep 02, 2026 · Updated 1 time
Summary
This trial compares two behavioral programs for people with chronic pain who take prescription opioids. One is cognitive behavioral therapy led by a psychologist, and the other is a peer-led self-management course. Researchers want to see if either approach helps people lower their opioid dose while keeping pain under control, compared with just tapering opioids on their own.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Cognitive behavioral therapy for chronic pain (pain-CBT) and a peer-led Chronic Pain Self-Management Program, compared with no behavioral treatment, all within the context of opioid tapering.
- What this could lead to
- If it works, this could give patients and doctors a clear, evidence-based way to lower opioid doses without losing pain control, pointing toward safer long-term pain management.
- What could go wrong
- The trial is large but still early, and results may not apply to everyone. Behavioral therapies require time and effort, and some participants may not benefit or may find it hard to stick with the program.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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1,462 people
The number who actually took part.
- Started
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Jul 2018
- Finished
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Nov 2023
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 85 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Chronic non-cancer pain (≥ 6 months in duration) * Currently receiving prescription opioids (≥ 10 MEDD) for ≥ 3 months Exclusion Criteria: * Unable to provide informed consent * Unable to participate in group treatments in a meaningful way (e.g., evident cognitive impairment or lack of English fluency) * Moderate to severe opioid use disorder
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Stanford University
Palo Alto, California, 94304, United States
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Other studies related to the condition(s) this trial covers.
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