Whole Health Options and Pain Education (wHOPE): A Pragmatic Trial Comparing Whole Health Team vs Primary Care Group Education to Promote Nonpharmacological Strategies to Improve Pain, Functioning, and Quality of Life in Veterans

TitleWhole Health Options and Pain Education (wHOPE): A Pragmatic Trial Comparing Whole Health Team vs Primary Care Group Education to Promote Nonpharmacological Strategies to Improve Pain, Functioning, and Quality of Life in Veterans
Publication TypeJournal Article
Year of Publication2020
AuthorsSeal, KH, Becker, WC, Murphy, JL, Purcell, N, Denneson, LM, Morasco, BJ, Martin, AM, Reddy, K, Van Iseghem, T, Krebs, EE, Painter, JM, Hagedorn, H, Pyne, JM, Hixon, J, Maguen, S, Neylan, TC, Borsari, B, DeRonne, B, Gibson, C, Matthias, MS, Frank, JW, Krishnaswamy, A, Li, Y, Bertenthal, D, Chan, A, Nunez, A, McCamish, N
JournalPain Med
Volume21
IssueSuppl 2
PaginationS91-S99
Date Published2020 Dec 12
ISSN1526-4637
KeywordsChronic Pain, Humans, Primary Health Care, Quality of Life, United States, United States Department of Veterans Affairs, Veterans
Abstract

BACKGROUND: The Whole Health model of the U.S. Department of Veterans Affairs (VA) emphasizes holistic self-care and multimodal approaches to improve pain, functioning, and quality of life. wHOPE (Whole Health Options and Pain Education) seeks to be the first multisite pragmatic trial to establish evidence for the VA Whole Health model for chronic pain care.

DESIGN: wHOPE is a pragmatic randomized controlled trial comparing a Whole Health Team (WHT) approach to Primary Care Group Education (PC-GE); both will be compared to Usual VA Primary Care (UPC). The WHT consists of a medical provider, a complementary and integrative health (CIH) provider, and a Whole Health coach, who collaborate with VA patients to create a Personalized Health Plan emphasizing CIH approaches to chronic pain management. The active comparator, PC-GE, is adapted group cognitive behavioral therapy for chronic pain. The first aim is to test whether the WHT approach is superior to PC-GE and whether both are superior to UPC in decreasing pain interference in functioning in 750 veterans with moderate to severe chronic pain (primary outcome). Secondary outcomes include changes in pain severity, quality of life, mental health symptoms, and use of nonpharmacological and pharmacological therapies for pain. Outcomes will be collected from the VA electronic health record and patient-reported data over 12 months of follow-up. Aim 2 consists of an implementation-focused process evaluation and budget impact analysis.

SUMMARY: This trial is part of the Pain Management Collaboratory, which seeks to create national-level infrastructure to support evidence-based nonpharmacological pain management approaches for veterans and military service personnel.

DOI10.1093/pm/pnaa366
Alternate JournalPain Med
PubMed ID33313734
PubMed Central IDPMC7825011
Grant ListUH3 AT009765 / AT / NCCIH NIH HHS / United States
UG3 AT009765 / AT / NCCIH NIH HHS / United States
UL1 TR001863 / TR / NCATS NIH HHS / United States
U24 AT009769 / AT / NCCIH NIH HHS / United States
IK2 HX001914 / HX / HSRD VA / United States