Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Mindfulness Text Messages to Support Medication Adherence and Pain Management

Official title: Integrating Mindfulness and mHealth Approaches for Treating Opioid Use Disorder and Chronic Pain

Run by University of New Mexico · NCT07711795 · Data updated 2026-11-12

This study tests whether daily reminder and mindfulness text messages can help people on medications for opioid use disorder with chronic pain stick to their treatment and better manage cravings and pain.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorUniversity of New Mexico
Academic / other
Locations1 site (Albuquerque, New Mexico)
StatusRecruiting
StartedApril 23, 2025
Main results expectedJuly 2027
Study endsOctober 2027
Registry record updatedJuly 17, 2026
Trial IDNCT07711795 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18 or older residing in the United States, initiating or restarting methadone or buprenorphine treatment, with chronic pain, who own a mobile phone and can access text messaging and study surveys.

Probably not a fit

Individuals without access to reliable mobile texting, not on methadone/buprenorphine therapy, or without chronic pain may derive little to no benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study evaluates two mindfulness text message strategies delivered alongside daily medication reminders for people starting or restarting methadone or buprenorphine treatment and living with chronic pain. Participants receive six weeks of mindfulness messages (two per day in one arm, four per day in another) plus 12 weeks of daily medication reminders, with message timing randomized across six daily windows. The trial examines adherence to medication, cravings, pain and pain interference, mindfulness, and withdrawal symptoms, comparing curriculum-based messages to randomized messages. Engagement with messages, state mindfulness, values-based living, substance misuse, and self-efficacy are secondary outcomes. Sixty adults across the United States will participate, with outcomes assessed through self-reported measures and questionnaires.

Why it matters

Potential benefit: If successful, participants may experience better medication adherence and reduced craving and pain, contributing to improved opioid use disorder management.

How similar studies have gone: Previous work suggests that mHealth text messages can support adherence and symptom management, but this specific dual-message mindfulness curriculum approach is novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
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

Where it's running

  • University of New Mexico
    Albuquerque, New Mexico, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.