Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07541599

Reaching Rural Veterans: Applying Mind-Body Skills for Pain Using a Whole Health Telehealth Intervention - UH3

Led by Minneapolis Veterans Affairs Medical Center · Updated on 2026-04-21

500

Participants Needed

1

Research Sites

139 weeks

Total Duration

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AI-Summary

What this Trial Is About

The goal of the RAMP mind-body program is to provide Veterans with information and tools that can help them manage their pain. The program explores the important connection between our bodies and minds, and how to use this special connection to manage pain more effectively.

CONDITIONS

Official Title

Reaching Rural Veterans: Applying Mind-Body Skills for Pain Using a Whole Health Telehealth Intervention - UH3

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years of age or older
  • Living in a rural area based on U.S. Health Services Research Administration criteria
  • Chronic pain with two qualifying pain diagnoses in the same category at least 90 days apart within the last 2 years
  • Self-reported pain on most days during the past 3 months
  • Brief Pain Inventory Interference subscale score of 4 or higher out of 10
  • Access to a device with internet connection
  • Willingness to participate in remote online sessions
  • Having an email address listed in the electronic health record
Not Eligible

You will not qualify if you...

  • Severe, poorly controlled psychiatric or substance use disorder
  • Active members of advisory panels for this study
  • Currently enrolled in another pain-related research study
  • Participation in a similar study
  • Participation in a similar multi-week, multi-modal complementary and integrative health program

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Minneapolis VAMC

Minneapolis, Minnesota, United States, 55417

Actively Recruiting

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Research Team

D

Diana Burgess, PhD

CONTACT

L

Lee Cross, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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