COMPLETED

Mobile & Online-Based Interventions to Lessen Pain

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 investigators will implement an international 2-arm online pragmatic feasibility randomized controlled trial (RCT) of a digital pain relief skills intervention "Empowered Relief: On-Demand" to reduce pain metrics, opioid craving, and opioid misuse. They will compare Empowered Relief to a no-skills digital health education ("Living Better") intervention in community-based individuals with comorbid chronic pain and prescription opioid misuse (N=220). Completion of the brief post-treatment survey is a binary measure of treatment engagement; treatment feasibility and appraisal are assessed with three items (satisfaction, perceived utility, and likelihood to use skills learned). Electronic surveys will measure opioid misuse behaviors, craving, and use; and pain intensity and psychological status at: baseline, immediately post-treatment; at post-treatment weeks 1 and 2; and months 1, 2, and 3.

Official Title

Mobile & Online-Based Interventions to Lessen Pain (MOBILE Relief) in People With Prescription Opioid Misuse

Quick Facts

Study Start:2023-08-23
Study Completion:2025-08-15
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT05152134

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. * Male and females 18 years of age or older
  2. * Chronic non-cancer pain (at least 6 months in duration)
  3. * Average pain intensity of at least 3 on the PROMIS SFV1.0 Pain Intensity 1a
  4. * Daily prescription opioid use (at least 10 morphine milliequivalent daily dose; MEDD) for at least 3 months
  5. * Opioid misuse (at least 6 on the Current Opioid Misuse Measure; COMM)
  6. * English fluency
  7. * Internet access
  1. * Gross cognitive impairment
  2. * Inability to complete study electronic surveys
  3. * Cannot currently be enrolled in a study or trial with Empowered Relief as a treatment/intervention

Contacts and Locations

Study Locations (Sites)

Stanford University
Palo Alto, California, 94304
United States

Collaborators and Investigators

Sponsor: Stanford University

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 Date2023-08-23
Study Completion Date2025-08-15

Study Record Updates

Study Start Date2023-08-23
Study Completion Date2025-08-15

Terms related to this study

Additional Relevant MeSH Terms

  • Chronic Pain
  • Opioid Misuse
  • Opioid Use Disorder