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N/A Completed N=40 Treatment

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

Source: ClinicalTrials.gov NCT06568250 ↗
Enrolled (actual)
40
Serious AEs
0.0%
Results posted
Feb 2026
Primary outcomePrimary: Participants Recruited — 40 Participants

Summary

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.

Outcome Measures

OutcomeResultp-value
PRIMARY
Participants Recruited
40
PRIMARY
Female Participants Recruited
21
PRIMARY
Racial/Ethnic Minoritized Participants Recruited
22
PRIMARY
Participant Satisfaction
26
PRIMARY
Participant Engagement
27
PRIMARY
Fidelity of Intervention Delivery
6
PRIMARY
Survey Response Rate
30

Eligibility Criteria

Inclusion Criteria

  • Veteran participants must be rural dwelling
  • Patient's Veterans Affairs (VA) primary care provider is in the Southeast region of the US
  • Email address in the VA electronic health record (EHR)
  • Report pain at least most days in the past 3 months
  • Brief Pain Inventory (BPI) Pain Interference subscale score of 4 or greater
  • Willingness and ability to complete study activities including meeting remotely via videoconferencing when program sessions are held

Exclusion Criteria

  • Participation in a prior project conducted by the study team on mindfulness for pain (NCT0456158) or an engagement activities advisor for the current project
  • Current enrollment in a research study for pain
  • Current enrollment in a similar facilitated, multi-week, multi-modal CIH program
  • 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)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT06568250). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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