New study tests Self-Management program to ease pain and boost opioid treatment
NCT ID NCT06855732
First seen Jun 27, 2026 · Last updated Aug 19, 2026 · Updated 2 times
Summary
This study tests a 12-week Pain Self-Management (PSM) program for people with chronic pain and opioid misuse or opioid use disorder. Researchers want to see if the program helps participants manage pain better and stay in treatment for opioid use. About 204 adults from primary care clinics will take part, with some receiving the PSM program and others getting standard care. Participants will complete surveys over 9 months to track their progress.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Pain Self-Management (PSM) program
- What this could lead to
- If it works, this could offer a practical, non-drug way to help people with chronic pain and opioid use disorder feel better and stay engaged in their recovery.
- What could go wrong
- This is a relatively small, early-stage trial comparing the program to usual care. The results may not apply to everyone, and there are risks like psychological distress from discussing difficult topics.
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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About 204 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2024
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- 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 years and older
- 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: In order to be eligible to participate in this study, an individual must meet all of the following criteria: 1. Adults at least 18 years old 2. Ability to speak, read, and understand English 3. Capable of providing informed consent 4. Access to phone and/or internet 5. Current (defined as at least 1 primary care visit in the past 3 years) or new (confirmed appointment) primary care patient at a participating clinic 6. Must meet criteria for OUD or opioid misuse based on at least one of the following: 1. OUD Misuse Screening score of 3 or more (sometimes or more) on at least one of the questions 2. Meets criteria for DSM-5 Opioid Use Disorder on MINI-J 3. Documented diagnosis of Opioid use Disorder (OUD) 7. Have bothersome (Grade 2) or high impact chronic pain (Grade 3), based on the Graded Chronic Pain Scale-Revised (GCPS-R) Exclusion Criteria: An individual who meets any of the following criteria will be excluded from participation in this study: 1. Under 18 years of age 2. Have cancer-related pain 3. Are currently in jail, prison, overnight/residential facility as required by court of law or have pending legal action that could prevent participation in study activities 4. Have received prescribed, administered, or dispensed MOUD (buprenorphine, methadone, naltrexone) as maintenance treatment for OUD (excluding acute or short-term (\< 7 days) use of these medications to manage opioid withdrawal or pain management) within the past 90 days 5. Had an intentional suicide attempt within the past 3 months The investigators will not exclude individuals with common comorbidities, such as depression, anxiety, or alcohol, methamphetamine, and other substance use disorders.
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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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Community Medicine, Inc.
Pittsburgh, Pennsylvania, 15213, United States
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Comprehensive Care Practice
Baltimore, Maryland, 21224, United States
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Harpers Ferry Family Medicine (WVU Medicine)
Harpers Ferry, West Virginia, 25425, United States
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Renaissance Family Practice - Aspinwall Office
Pittsburgh, Pennsylvania, 15215, United States
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Renaissance Family Practice - Glenshaw Office
Glenshaw, Pennsylvania, 15223, United States
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Renaissance Family Practice - Hampton Office
Allison Park, Pennsylvania, 15101, United States
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Renaissance Family Practice - Harmarville Office
Pittsburgh, Pennsylvania, 15238, United States
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Renaissance Family Practice - Millvale Office
Pittsburgh, Pennsylvania, 15209, United States
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Renaissance Family Practice - Penn Hills Office
Verona, Pennsylvania, 15147, United States
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Renaissance Family Practice - RIDC Office
Blawnox, Pennsylvania, 15238, United States
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St. Joseph's Rural Health Clinic (WVU Medicine)
Buckhannon, West Virginia, 26201, United States
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UPMC General Internal Medicine-Montefiore
Pittsburgh, Pennsylvania, 15213, United States
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UPMC General Internal Medicine-Shadyside (Shea Medical Center)
Pittsburgh, Pennsylvania, 15232, United States
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UPMC General Internal Medicine-South
West Mifflin, Pennsylvania, 15122, United States
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UPMC General Internal Medicine-Turtle Creek
Turtle Creek, Pennsylvania, 15145, United States
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WVU Medicine Primary Care
Shepherdstown, West Virginia, 25419, United States
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WVU Medicine University Town Centre
Morgantown, West Virginia, 26501, United States
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