Can daily text messages help curb opioid cravings and ease chronic pain?

NCT ID NCT07711795

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jul 17, 2026 · Last updated Jul 17, 2026

Summary

This study tests whether daily mindfulness text messages can help people taking medication for opioid use disorder who also have chronic pain. Participants receive medication reminders and either two or four mindfulness messages per day for six weeks, along with brief surveys throughout the day. The goal is to see if these messages improve medication adherence, reduce cravings and pain, and increase mindfulness.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
mindfulness text messages based on Acceptance and Commitment Therapy and Mindfulness-Based Relapse Prevention
What this could lead to
If effective, this approach could offer a low-cost, scalable way to support medication adherence and reduce cravings and pain in people with opioid use disorder.
What could go wrong
This is a small, early-stage trial focused on feasibility and engagement, not on proving clinical outcomes. The benefits may not be large or lasting.

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

About 60 people

The number the study aims to enrol. It can still change while the study runs.

Started

Apr 2025

Expected to finish

Oct 2027

An estimate. End dates often move.

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age 18 years or older * Reside in the United States * Own or have access to a mobile phone capable of sending and receiving text messages * Have reliable internet access to complete study surveys * Be willing and able to comply with all study procedures and remain available for the duration of the study * Be interested in receiving medication reminders and mindfulness text messages * Be within 2 months of initiating or restarting methadone or buprenorphine treatment for opioid use * Report chronic pain (pain lasting at least 3 months) * Live in the United States Exclusion Criteria: * None

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Conditions

The condition(s) this trial relates to.

Chronic Pain chronic pain syndrome Medication Adherence opiate dependence

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.

  1. The study's own enquiry address

    This study publishes an address for enquiries. See it below .

  2. The places running it

    1 site. The list below names each one and where it is.

  3. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

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  4. A doctor treating you

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Contacts and locations

Study contacts

  • Contact

    Email: •••••@•••••

Locations

  • University of New Mexico

    RECRUITING

    Albuquerque, New Mexico, 87131, United States

    Contact Email: •••••@•••••

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