Phone coaching may curb Long-Term pain after joint surgery
NCT ID NCT04979429
First seen Jul 02, 2026 ยท Last updated Jul 02, 2026
Summary
This study tests a telephone-based pain self-management program for veterans scheduled for hip, knee, or shoulder joint replacement. The program teaches cognitive-behavioral techniques to help patients manage pain and reduce opioid use after surgery. Researchers will compare pain levels and how quickly patients stop taking opioids between those who receive the program and those who get standard care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Perioperative Pain Self-management (PePS) program
- What this could lead to
- If effective, this program could offer a simple, non-drug way to prevent long-term pain and reduce reliance on opioids after joint replacement surgery.
- What could go wrong
- This is a behavioral intervention tested in a specific VA population, so results may not apply to everyone. The program requires patient engagement and may not work for all types of surgery.
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
-
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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401 people
The number who actually took part.
- Started
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Aug 2021
- Finished
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Jun 2026
- Lead sponsor
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A government agency
The lead sponsor is a US federal agency other than the NIH.
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 100 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: * scheduled for total hip, knee, or shoulder joint arthroplasty through the Iowa City, IA, Des Moines, IA, Minneapolis, IA, or Milwaukee WI, VA medical centers Exclusion Criteria: * inability to complete study forms/procedures because of a language/literacy barrier * active bipolar or psychotic disorder * history of brain injury * dementia * CBT therapy within the past year * lack of access to a telephone for PePS sessions
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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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Iowa City VA Health Care System, Iowa City, IA
Iowa City, Iowa, 52246-2292, United States
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Minneapolis VA Health Care System, Minneapolis, MN
Minneapolis, Minnesota, 55417-2309, United States
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