RECRUITING

Tele-Collaborative Outreach to Rural Patients with Chronic 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

This is a randomized controlled trial comparing the effectiveness of a remotely delivered collaborative care intervention for chronic pain versus a minimally enhanced control group. The specific aims of the study are: (1) compare the effectiveness of tele-collaborative pain care vs. minimally enhanced usual care to improve pain interference over 12 months of follow-up, and (2) oversample women and rural veterans of minoritized race/ethnicity to test heterogeneity of treatment effects across birth sex and race/ethnicity.

Official Title

Tele-Collaborative Outreach to Rural Patients with Chronic Pain: the CORPs Trial

Quick Facts

Study Start:2023-10-02
Study Completion:2027-09
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06091202

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. * U.S. Veteran
  2. * Rural Residence based on Rural Urban Commuting Area codes
  3. * High Impact Chronic pain, determined through a phone screening
  4. * Access to landline or cell phone
  5. * English Speaking
  1. * Cognitive impairment that would impact participation in the study
  2. * Plans to move in the next 3 months
  3. * Surgery in the past 3 months
  4. * In long-term inpatient or hospice care
  5. * Terminal illness (defined as life expectancy of less than 12 months)
  6. * Active participation in another pain intervention study

Contacts and Locations

Study Contact

Natassja Pal, BS
CONTACT
503-220-8262
natassja.pal@va.gov

Principal Investigator

Travis Lovejoy, PhD, MPH
PRINCIPAL_INVESTIGATOR
Oregon Health & Science University, VA Portland Health Care System
Benjamin Morasco, PhD
PRINCIPAL_INVESTIGATOR
Oregon Health & Science University, VA Portland Health Care System

Study Locations (Sites)

VA Minneapolis Health Care System
Minneapolis, Minnesota, 55417
United States
VA Portland Health Care System
Portland, Oregon, 97239
United States
VA Tennessee Valley Health Care System
Nashville, Tennessee, 37212
United States
VA North Texas Health Care System
Dallas, Texas, 75216
United States

Collaborators and Investigators

Sponsor: Oregon Health and Science University

  • Travis Lovejoy, PhD, MPH, PRINCIPAL_INVESTIGATOR, Oregon Health & Science University, VA Portland Health Care System
  • Benjamin Morasco, PhD, PRINCIPAL_INVESTIGATOR, Oregon Health & Science University, VA Portland Health Care System

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 Date2023-10-02
Study Completion Date2027-09

Study Record Updates

Study Start Date2023-10-02
Study Completion Date2027-09

Terms related to this study

Keywords Provided by Researchers

  • Rural
  • Pain
  • CIH
  • Veteran

Additional Relevant MeSH Terms

  • Chronic Pain