RECRUITING

M2VA Pain Care Pathway

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 goal of this 2-cohort, cluster randomized, type 2 hybrid trial is to test the effectiveness, cost-effectiveness and patient-level effects of an implementation facilitation strategy in helping M2VA case managers adopt a Military2VA Pain Care Pathway (M2VAPCP) intervention. The main questions it aims to answer are: Will adding implementation facilitation to training-as-usual for M2VAPCP result in a higher proportion of Veterans who receive M2VAPCP compared to training-as-usual alone? Will adding implementation facilitation to training-as-usual for M2VAPCP result in better adherence to the M2VAPCP protocol compared to training-as-usual alone? Will implementation facilitation improve Veterans' clinical outcomes (pain, risky substance use) and increase the number of non-pharmacological pain treatments used compared to training-as-usual alone?

Official Title

Implementation Facilitation of Screening, Brief Intervention, and Referral to Treatment for Pain Management for Veterans Separating From Military Service

Quick Facts

Study Start:2024-09-18
Study Completion:2028-07
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06526143

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. * Study enrollment is within one year of ending military service
  2. * Has filed a service-connection claim for an MSD (back, neck, knee, or shoulder condition)
  3. * Lives within the catchment area of a participating site
  1. * Reports being unable to complete planned study assessments because of anticipated incapacity, incarceration, or other reason
  2. * Does not have a landline or cell phone to complete study assessments
  3. * Is unable to provide informed consent
  4. * Still on active duty

Contacts and Locations

Study Contact

Christina Lazar, MPH
CONTACT
203-932-5711
christina.lazar@yale.edu

Principal Investigator

Marc Rosen, MD
PRINCIPAL_INVESTIGATOR
Yale University

Study Locations (Sites)

VA Connecticut Healthcare System (VACHS)
West Haven, Connecticut, 06516
United States

Collaborators and Investigators

Sponsor: Yale University

  • Marc Rosen, MD, PRINCIPAL_INVESTIGATOR, Yale 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 Date2024-09-18
Study Completion Date2028-07

Study Record Updates

Study Start Date2024-09-18
Study Completion Date2028-07

Terms related to this study

Keywords Provided by Researchers

  • case management
  • SBIRT

Additional Relevant MeSH Terms

  • Pain
  • Substance Use
  • Opioid Misuse
  • Quality of Life