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

Not Applicable
Recruiting
Conditions
Chronic Pain
Registration Number
NCT06568250
Lead Sponsor
Minneapolis Veterans Affairs Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria

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

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Number of Participants Recruited;Percentage of Female and Racial/Ethnic Minoritized Participants Recruited;Percentage of Participants Who Report Being Somewhat Satisfied or Very Satisfied with the Program on a 7-point Scale;Percentage of Participants Who Attend/Engage with Recommended Number of Sessions;Intervention Fidelity Based on Observation By Trained Raters;Percentage of Participants Who Complete Post-Treatment Data Collection
Secondary Outcome Measures
NameTimeMethod
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