COMPLETED

Reaching Rural Veterans: Applying Mind-Body Skills for Pain Using a Whole Health Telehealth Intervention - UG3 Pilot Study

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 project addresses the significant challenge of providing evidence-based non-pharmacologic pain management to rural-dwelling Veterans in the VA healthcare system who have chronic pain. For this preparatory phase (UG3), the investigators will conduct a single-arm pilot study of 40 rural VA patients with chronic pain to assess study feasibility (recruitment and retention), intervention feasibility (fidelity of intervention delivery and participant engagement rates), acceptability, and effectiveness at addressing pre-defined capabilities, opportunities and motivations.

Official Title

Reaching Rural Veterans: Applying Mind-Body Skills for Pain Using a Whole Health Telehealth Intervention

Quick Facts

Study Start:2024-08-07
Study Completion:2025-03-24
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06568250

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. * Veteran participants must be rural dwelling
  2. * Patient's Veterans Affairs (VA) primary care provider is in the Southeast region of the US
  3. * Email address in the VA electronic health record (EHR)
  4. * Report pain at least most days in the past 3 months
  5. * Brief Pain Inventory (BPI) Pain Interference subscale score of 4 or greater
  6. * Willingness and ability to complete study activities including meeting remotely via videoconferencing when program sessions are held
  1. * Participation in a prior project conducted by the study team on mindfulness for pain (NCT0456158) or an engagement activities advisor for the current project
  2. * Current enrollment in a research study for pain
  3. * Current enrollment in a similar facilitated, multi-week, multi-modal CIH program
  4. * Severe, poorly controlled psychiatric or substance use disorder (based on chart review using structured checklists, conducted by trained staff who are trained and supervised by a clinical psychologist)

Contacts and Locations

Study Locations (Sites)

Minneapolis VAMC
Minneapolis, Minnesota, 55417
United States

Collaborators and Investigators

Sponsor: Minneapolis Veterans Affairs Medical Center

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 Date2024-08-07
Study Completion Date2025-03-24

Study Record Updates

Study Start Date2024-08-07
Study Completion Date2025-03-24

Terms related to this study

Keywords Provided by Researchers

  • chronic pain
  • mindfulness
  • complementary therapies
  • models, biopsychosocial
  • rural Veterans health

Additional Relevant MeSH Terms

  • Chronic Pain