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Transcutaneous Electrical Nerve Stimulation Reduces Movementā€Evoked Pain and Fatigue: A Randomized, Controlled Trial

Authors :
Barbara A. Rakel
Ericka N. Merriwether
Katharine M. Geasland
M. Bridget Zimmerman
Meenakshi Golchha
Leslie J. Crofford
Kathleen A. Sluka
Jon M. Williams
Jennie Embree
Ruth L. Chimenti
Dana L. Dailey
Carol G.T. Vance
Source :
Arthritis & Rheumatology. 72:824-836
Publication Year :
2020
Publisher :
Wiley, 2020.

Abstract

OBJECTIVE Fibromyalgia (FM) is characterized by pain and fatigue, particularly during physical activity. Transcutaneous electrical nerve stimulation (TENS) activates endogenous pain inhibitory mechanisms. This study was undertaken to investigate if using TENS during activity would improve movement-evoked pain and other patient-reported outcomes in women with FM. METHODS Participants were randomly assigned to receive active TENS (n = 103), placebo TENS (n = 99), or no TENS (n = 99) and instructed to use it at home during activity 2 hours each day for 4 weeks. TENS was applied to the lumbar and cervicothoracic regions using a modulated frequency (2-125 Hz) at the highest tolerable intensity. Participants rated movement-evoked pain (primary outcome measure) and fatigue on an 11-point scale before and during application of TENS. The primary outcome measure and secondary patient-reported outcomes were assessed at baseline (time of randomization) and at 4 weeks. RESULTS After 4 weeks, a greater reduction in movement-evoked pain was reported in the active TENS group versus the placebo TENS group (group mean difference -1.0 [95% confidence interval -1.8, -0.2]; P = 0.008) and versus the no TENS group (group mean difference -1.8 [95% confidence interval -2.6, -1.0]; P < 0.0001). A reduction in movement-evoked fatigue was also reported in the active TENS group versus the placebo TENS group (group mean difference -1.4 [95% confidence interval -2.4, -0.4]; P = 0.001) and versus the no TENS group (group mean difference -1.9 [95% confidence interval -2.9, -0.9]; P =

Details

ISSN :
23265205 and 23265191
Volume :
72
Database :
OpenAIRE
Journal :
Arthritis & Rheumatology
Accession number :
edsair.doi.dedup.....24d08c7551c109eff23511885d4a4486