RECRUITING

Optimizing Chronic Pain Care With Mindfulness and Chronic Pain Management Visits

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The primary aim of this implementation-effectiveness trial is to examine the effectiveness of Mindfulness-Oriented Recovery Enhancement (MORE) and patient-centered chronic pain management visits in primary care as interventions to reduce chronic pain, improve quality of life, and reduce opioid-related harms among chronic pain patients on long-term opioid therapy.

Official Title

Optimizing Chronic Pain Care With Mindfulness and Chronic Pain Management Visits

Quick Facts

Study Start:2025-02-25
Study Completion:2028-05-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06387290

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age 18 +
  2. * Current chronic pain diagnosis (pain for ≥3 months) determined by physician assessment
  3. * Current use of opioids for ≥3 months
  4. * Score \>=3 on the Pain Enjoyment General Activity scale
  5. * Score \>=9 on the Current Opioid Misuse Measure OR lifetime psychiatric or substance use disorder diagnosis OR benzodiazepine use OR history of overdose OR physician determination that risks of opioid use may outweigh the benefits of opioid use
  1. * Chronic pain due to a cancer diagnosis
  2. * Active suicidal intent, schizophrenia, psychotic disorder
  3. * Prior experience with Mindfulness-Based Stress Reduction, Mindfulness-Based Cognitive Therapy, Mindfulness-Based Relapse Prevention, or Mindfulness-Oriented Recovery Enhancement

Contacts and Locations

Study Contact

Thanusha Puvananayagam, MPH
CONTACT
732-235-4341
puvanath@rwjms.rutgers.edu
Taylor Scott, MSW
CONTACT
732-235-7453
taylor.m.scott@rutgers.edu

Study Locations (Sites)

UCSD Health
La Jolla, California, 92037
United States
Rutgers University Primary Care Clinics
New Brunswick, New Jersey, 08901
United States
University of Utah Primary Care Clinics
Salt Lake City, Utah, 84112
United States

Collaborators and Investigators

Sponsor: University of Utah

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-02-25
Study Completion Date2028-05-01

Study Record Updates

Study Start Date2025-02-25
Study Completion Date2028-05-01

Terms related to this study

Additional Relevant MeSH Terms

  • Chronic Pain
  • Prescription Opioid Misuse
  • Substance-Related Disorders
  • Pain
  • Narcotic-Related Disorders
  • Chemically-Induced Disorders
  • Mental Disorders
  • Opioid-Related Disorders
  • Neurologic Manifestations