New tool aims to make opioid tapering safer and less scary
NCT ID NCT07202026
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study aims to create a decision aid to help patients on long-term opioid therapy and their doctors have better conversations about safely reducing or stopping opioids. Researchers will interview patients and doctors to understand their experiences, then test the tool with 30 patients. The goal is to reduce fear, improve trust, and avoid harms like untreated pain or relapse to illicit opioids.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Patient-centered Decision Aid (behavioral intervention)
- What this could lead to
- If successful, this could lead to a tool that helps patients and doctors have better conversations about safely reducing opioid use, potentially reducing harm from forced tapering.
- What could go wrong
- This is a small pilot study with only 30 participants, so results may not apply to everyone. The decision aid may not work as well in real-world settings or for diverse populations.
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 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2025
- Expected to finish
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Sep 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.
EHR-based inclusion criteria: * age 18 or older * LTOT in the past 18 months (LTOT is ≥60 days of ≥50 MEDs day in each of 2 consecutive 90-day periods with medication treatment for OUD excluded) Inclusion criteria confirmed by participant * Have been taking opioids for chronic pain for at least 6 months * Able to speak and read English EHR-based exclusion criteria: * cancer diagnosis in the last 5 years (excluding non-melanoma skin cancers) * current palliative or hospice care * cognitive disability * psychiatric hospitalization in the last year * surgery in the last 6 months * current residence in an inpatient rehabilitation or skilled nursing facility Exclusion criteria determined by study \- participated in an interview for Aim 1 of this study
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Kaiser Permanente Washington Health Research Institute
Seattle, Washington, 98101, United States
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