OBJECTIVE: The purpose of this study was to identify exercise protocols incorporating isometric contractions that provide pain relief in women with fibromyalgia. DESIGN: A before-after trial. SETTING: A physical therapy department in an academic setting. PARTICIPANTS: Fifteen women (mean ± SD, 52±11y) with fibromyalgia. INTERVENTIONS: Subjects completed 4 sessions: 1 familiarization and 3 experimental. The following randomized experimental sessions involved the performance of isometric contractions with the elbow flexor muscles that varied in intensity and duration: (1) 3 maximal voluntary contractions (MVCs), (2) 25% MVC held to task failure, and (3) 25% MVC held for 2 minutes. MAIN OUTCOME MEASURES: Experimental pain (pain threshold and pain rating), Fibromyalgia Impact Questionnaire, and fibromyalgia pain intensity (visual analog scale). RESULTS: After all 3 isometric contractions, there was considerable variability between subjects in the pain response. Based on the changes in experimental pain, subjects were divided into 3 groups (increase, decrease, no change in pain). Multiple regression analysis revealed that age, baseline experimental pain, and change in fibromyalgia pain intensity were significant predictors of the experimental pain response after the isometric contractions. CONCLUSIONS: We identified subgroups of women with fibromyalgia based on how they perceived pain after isometric contractions. The greatest pain relief for women with fibromyalgia occurred at a younger age and in women with the greatest experimental pain before exercise. Additionally, we established a link between experimental and clinical pain relief after the performance of isometric contractions.
RCT Entities:
OBJECTIVE: The purpose of this study was to identify exercise protocols incorporating isometric contractions that provide pain relief in women with fibromyalgia. DESIGN: A before-after trial. SETTING: A physical therapy department in an academic setting. PARTICIPANTS: Fifteen women (mean ± SD, 52±11y) with fibromyalgia. INTERVENTIONS: Subjects completed 4 sessions: 1 familiarization and 3 experimental. The following randomized experimental sessions involved the performance of isometric contractions with the elbow flexor muscles that varied in intensity and duration: (1) 3 maximal voluntary contractions (MVCs), (2) 25% MVC held to task failure, and (3) 25% MVC held for 2 minutes. MAIN OUTCOME MEASURES: Experimental pain (pain threshold and pain rating), Fibromyalgia Impact Questionnaire, and fibromyalgia pain intensity (visual analog scale). RESULTS: After all 3 isometric contractions, there was considerable variability between subjects in the pain response. Based on the changes in experimental pain, subjects were divided into 3 groups (increase, decrease, no change in pain). Multiple regression analysis revealed that age, baseline experimental pain, and change in fibromyalgia pain intensity were significant predictors of the experimental pain response after the isometric contractions. CONCLUSIONS: We identified subgroups of women with fibromyalgia based on how they perceived pain after isometric contractions. The greatest pain relief for women with fibromyalgia occurred at a younger age and in women with the greatest experimental pain before exercise. Additionally, we established a link between experimental and clinical pain relief after the performance of isometric contractions.
Authors: José V Pardo; Robert C Larson; Rachel J Spencer; Joel T Lee; Jeffrey D Pasley; Carolyn J Torkelson; Alice A Larson Journal: Clin J Pain Date: 2019-05 Impact factor: 3.442
Authors: Kevin Pacheco-Barrios; Anna Carolyna Gianlorenço; Roberto Machado; Marcos Queiroga; Huiyan Zeng; Emad Shaikh; Yiling Yang; Beatriz Nogueira; Luis Castelo-Branco; Felipe Fregni Journal: Princ Pract Clin Res Date: 2020-09-16
Authors: Angela J Busch; Sandra C Webber; Mary Brachaniec; Julia Bidonde; Vanina Dal Bello-Haas; Adrienne D Danyliw; Tom J Overend; Rachel S Richards; Anuradha Sawant; Candice L Schachter Journal: Curr Pain Headache Rep Date: 2011-10
Authors: Julia Bidonde; Angela J Busch; Candice L Schachter; Tom J Overend; Soo Y Kim; Suelen M Góes; Catherine Boden; Heather Ja Foulds Journal: Cochrane Database Syst Rev Date: 2017-06-21