Pain Care at Home to Amplify Function (Pain CHAMP)

Description

This project aims to test simultaneously the effectiveness of telemedicine and collaborative management (TCM) vs. TCM plus Cooperative Pain Education and Self-Management (COPES) on patient level outcomes and the impact of site-tailored Implementation Facilitation to work toward long term opioid therapy dose reduction. Pain CHAMP is a patient-level randomized hybrid II effectiveness-implementation trial comparing TCM vs. TCM + COPES on the primary composite outcome of pain interference and OUD/misuse symptoms.

Conditions

Opioid Use Disorder, Opioid Misuse, Chronic Pain

Study Overview

Study Details

Study overview

This project aims to test simultaneously the effectiveness of telemedicine and collaborative management (TCM) vs. TCM plus Cooperative Pain Education and Self-Management (COPES) on patient level outcomes and the impact of site-tailored Implementation Facilitation to work toward long term opioid therapy dose reduction. Pain CHAMP is a patient-level randomized hybrid II effectiveness-implementation trial comparing TCM vs. TCM + COPES on the primary composite outcome of pain interference and OUD/misuse symptoms.

Pain Care at Home to Amplify Function (Pain CHAMP)

Pain Care at Home to Amplify Function (Pain CHAMP)

Condition
Opioid Use Disorder
Intervention / Treatment

-

Contacts and Locations

Little Rock

Little Rock VAMC, Little Rock, Arkansas, United States, 72205

Aurora

Eastern Colorado HCS, Aurora, Colorado, United States, 80045

West Haven

VA Connecticut HCS, West Haven, Connecticut, United States, 06516

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Engaged in TCM intervention (with or without COPES)
  • * Engaged with a participating study site
  • * Not engaged in TCM intervention
  • * Not engaged with a participating study site

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Yale University,

William Becker, MD, PRINCIPAL_INVESTIGATOR, Yale University

Study Record Dates

2027-12-15