Healing Opioid Misuse and Pain Through Engagement (HOPE) Trial

Last updated: June 11, 2024
Sponsor: University of New Mexico
Overall Status: Active - Recruiting

Phase

N/A

Condition

Chronic Pain

Pain

Opioid Use Disorder

Treatment

Enhance Usual Care (EUC)

Acceptance and Commitment Therapy + Mindfulness Based Relapse Prevention (ACT + MBRP)

Clinical Study ID

NCT05571917
2206006784
RM1DA055301
  • Ages > 18
  • All Genders

Study Summary

This study is a multisite randomized clinical trial of a treatment designed to reduce pain interference while simultaneously addressing relapse prevention among individuals who have co-occurring chronic pain and Opioid Use Disorder (OUD). This study will recruit approximately 160 individuals who are currently being treated in clinics specializing in the physician management of OUD. To increase generalizability of study findings and increase internal validity of the physician management component of treatment, all participants will be stabilized on buprenorphine for OUD as part of their usual clinical care. Individuals will be randomized to either: (1) enhanced usual care or (2) the integrated ACT + MBRP treatment. The investigators hypothesize that: (1) the combination of ACT + MBRP in buprenorphine-prescribed patients with chronic pain will be more efficacious across primary and secondary outcome measures in comparison to Enhanced Usual Care and (2) examination of treatment mechanism data will indicate treatment-related changes that are consistent with the theoretical models of ACT+MBRP.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Stabilized on a dose of buprenorphine for a period of at least 1 month.Buprenorphine stabilization will be defined as a consistent dose for at least 30consecutive days.

  2. Willing to comply with all study procedures and be available for the duration of thestudy.

  3. Aged 18 years or older.

  4. Enrolled as a patient in one of the participating clinics.

  5. Presence of chronic pain for > 6 months in duration.

Exclusion

Exclusion Criteria:

  1. Current or past diagnosis of schizophrenia, delusional disorder, psychotic ordissociative disorders.

  2. Unable to read English.

  3. Have a substance use disorder requiring a higher level of care than outpatienttreatment (e.g., severe alcohol use disorder requiring inpatient detoxification).

Study Design

Total Participants: 160
Treatment Group(s): 2
Primary Treatment: Enhance Usual Care (EUC)
Phase:
Study Start date:
May 05, 2023
Estimated Completion Date:
December 31, 2026

Study Description

Opioid prescription in the treatment of chronic pain is frequent and carries a consequent risk of poor treatment outcome, as well as higher morbidity and mortality in a clinically significant number of patients, particularly those who meet criteria for OUD. Despite the alarming increases in opioid misuse and OUD nationally, there are few treatment options available that target both pain-related interference and OUD in an integrated fashion among patients with chronic pain. To date, there are no evidence-based treatment options that aim to minimize pain interference while simultaneously addressing OUD among individuals with medication prescribed for OUD.

The present trial builds upon a pilot study that tested the feasibility of integrating two empirically-supported psychosocial interventions, ACT to reduce pain interference and MBRP to reduce opioid misuse. Following successful integration of the interventions, outcome analyses found that the integrated ACT + MBRP intervention reduced both pain interference and opioid misuse at a 6-month follow-up in comparison to physician management alone.

This study is a multisite randomized clinical trial that will recruit approximately 160 individuals who are currently being treated in clinics specializing in the physician management of OUD. To increase generalizability of study findings and increase internal validity of the physician management component of treatment, all participants will be stabilized on buprenorphine for OUD as part of their usual clinical care. Individuals will be randomized to either: (1) enhanced usual care or (2) the integrated ACT + MBRP treatment.

The primary outcome, pain interference, will be assessed at the end of the active treatment phase and at 6- and 12-month follow-ups. Secondary outcomes will include pain intensity, depression, and pain-related fear, and an exploratory outcome of self-report of substance use with urine testing for confirmation. Treatment mechanism variables, including chronic pain acceptance, engagement in values-based action, and opioid craving will be assessed weekly during the active phase of treatment.

Our overall hypotheses are that: (1) the combination of ACT + MBRP in buprenorphine-prescribed patients with chronic pain will be more efficacious across primary and secondary outcome measures in comparison to EUC and (2) examination of treatment mechanism data will indicate treatment-related changes that are consistent with the theoretical models of ACT+MBRP.

Connect with a study center

  • University of Michigan

    Ann Arbor, Michigan 48109
    United States

    Active - Recruiting

  • University of New Mexico

    Albuquerque, New Mexico 87131
    United States

    Active - Recruiting

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