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A Study on the Effects of Dry Needling in Multiple Sclerosis Patients With Spasticity: Protocol of a Randomized Waitlist-Controlled Trial Publisher Pubmed



Motamedzadeh O1, 2 ; Ansari NN1, 2, 3 ; Naghdi S1, 2 ; Azimi A4 ; Mahmoudzadeh A5 ; Calvo S6 ; Herrero P7
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Authors Affiliations
  1. 1. Sports Medicine Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Department of Physiotherapy, School of Rehabilitation, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Research Center for War-affected People, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. MS Research Center, Neurosciences Institute, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Musculoskeletal Research Center, Faculty of Rehabilitation Sciences, Isfahan University of Medical Sciences, Isfahan, Iran
  6. 6. iPhysio Research Group, Universidad San Jorge. Villanueva de Gallego, Zaragoza, Spain
  7. 7. Department of Physiatry and Nursing, Faculty of Health Sciences, University of Zaragoza, Zaragoza, Spain

Source: JAMS Journal of Acupuncture and Meridian Studies Published:2021


Abstract

Background: Spasticity is a common symptom in multiple sclerosis (MS). Dry needling (DN) has been considered a useful method for the treatment of spasticity; however, there are no studies on the effects of DN on spasticity in patients with MS. We propose a study protocol aiming to investigate the effects of DN on spasticity in patients with MS. Methods: MS patients with plantar flexor spasticity will be recruited. Participants will be randomly assigned to the DN group, where they will be receiving a single session of DN, one minute for each head of gastrocnemius muscle, or to the waiting list control group with no intervention. Primary outcome measures are the Modified Ashworth Scale (MAS) for gastrocnemius spasticity, passive resistive torque, and podography for foot pressure distribution. The ankle active and passive range of dorsiflexion and Timed Up and Go tests are the secondary outcome measures. All outcomes will be measured at baseline, immediately after the intervention, and one week later. A mixed-model, general linear model, and two-way repeated-measures ANOVA will be used to compare the quantitative variables between groups and within groups at the measurement time points. The MAS ordinal measure of spasticity will be compared between groups using the Kruskal-Wallis test, and both the Friedman test and Wilcoxon test will be used for within-group changes. Discussion: This study will provide primary evidence on the effects of DN on gastrocnemius muscle spasticity and gait in patients with MS. © 2021 Korean Pharmacopuncture Institute. All rights reserved.
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