The Fibromyalgia Transcutaneous Electrical Nerve Stimulation in Physical Therapy Study Protocol: A Multisite Embedded Pragmatic Trial

Author:

Post Andrew A1ORCID,Dailey Dana L12,Bayman Emine O345,Chimenti Ruth L1ORCID,Costigan Michele3,Franck Carla6,Huff Trevis3,Johnson Elizabeth7,Koepp Maxine3,Lafontant David-Erick34,McCabe Megan E34,Neill-Hudson Tina3,Vance Carol G T1,Van Gorp Barb1,Zimmerman Bridget M3,Ecklund Dixie3,Crofford Leslie J7,Sluka Kathleen A1ORCID

Affiliation:

1. Department of Physical Therapy and Rehabilitation Science, The University of Iowa Roy J and Lucille A Carver College of Medicine , Iowa City, Iowa , USA

2. Physical Therapy Department, St. Ambrose University , Davenport, Iowa , USA

3. The University of Iowa Clinical Trials Statistical and Data Management Center , Iowa City Iowa , USA

4. Department of Biostatistics, The University of Iowa , Iowa City, Iowa , USA

5. Department of Anesthesia, The University of Iowa , Iowa City, Iowa , USA

6. Kepros Physical Therapy , Cedar Rapids, Iowa , USA

7. Vanderbilt University Medical Center, Division of Rheumatology and Immunology , Nashville, Tennessee , USA

Abstract

Abstract Objectives Transcutaneous electrical nerve stimulation (TENS) is a nonpharmacological intervention that provides an electrical current through the skin to produce analgesia. The primary purpose of this study is to examine if the addition of TENS to routine physical therapy improves movement-evoked pain in individuals with fibromyalgia in a physical therapy clinical setting. Methods Fibromyalgia TENS in Physical Therapy Study is a phase III embedded pragmatic clinical trial funded through the National Institutes of Health Helping to End Addiction Long-Term Initiative. This trial will utilize a randomized cluster design that includes more than 110 physical therapists in 24 to 30 physical therapy clinics within 6 health care systems and 7 states. Clinics will be randomized to TENS or No-TENS, stratified by health care system and clinic size. The plan is to enroll 600 participants, with all participants completing physical therapy as prescribed by their physical therapist. Participants at TENS clinics will utilize TENS for a minimum of 2-hour per day while at the physical therapy clinic and at home when active. The primary outcome is reduction in movement-evoked pain from baseline to day 60 on an 11-point numeric rating scale when participants sit and stand 5 times (Sit and Stand Test). Secondary outcomes include resting pain and fatigue, pain interference, fibromyalgia disease activity, movement-evoked fatigue, multidimensional assessment of fatigue, rapid assessment of physical activity, patient global impression of change, and common data elements shared across studies supported through the Helping to End Addiction Long-Term Initiative. Impact The findings from this study will provide effectiveness data on TENS for individuals with fibromyalgia for health care policymakers, clinicians, and insurers. Data from this study will also inform future pragmatic trials for nonpharmacological interventions and chronic musculoskeletal pain conditions.

Funder

National Institutes of Health

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Management of Pain to Reduce Opioid Prescribing Resource Coordinating Center

Publisher

Oxford University Press (OUP)

Subject

Physical Therapy, Sports Therapy and Rehabilitation

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