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Dry Needling and Functional Improvement

OverviewStructured DataIssuesContributors

Contents

clinicaltrials.gov/study/NCT02838394
Is a
‌
Clinical study
0

Clinical Study attributes

NCT Number
NCT028383940
Health Conditions in Trial
‌
Myofascial pain syndrome
0
Trial Recruitment Size
400
Trial Sponsor
Brigham Young University
Brigham Young University
0
Clinical Trial Start Date
2016
0
Primary Completion Date
2018
0
Study Completion Date
2018
0
Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Treatment0
Intervention Type
Other0
Procedure0
Intervention Name
Sham dry needling0
Dry needling0
Interventional Trial Phase
Not Applicable0
Official Name
Does Site-specific Trigger Point Dry Needling Evoke Segmental Neuromodulation in the Lower Extremity and if so, do These Changes Make an Impact on the Subject's Disability?0
Last Updated
January 18, 2018
0
Allocation Type
Randomized0
Intervention Model
Parallel Assignment0
Masking Type
Single0
Masked Party
Participant0
Study summary

Dry Needling (DN) is a skilled intervention that uses acupuncture filiform needles that are inserted into myofascial trigger points or other tissues underneath the skin. It is used to treat myofascial or neuromusculoskeletal pain and to improve movement impairments. Although more and more physical therapists add this treatment tool to their skill box, there is uncertainty about its working mechanism and its efficacy. The latter is partially due to the challenging task of finding and using a true control or sham treatment. The investigators will use blunted needles, which will not perforate the skin, as sham treatment. This study will assess if DN of a trigger point in the gluteal muscles increases pain pressure threshold in that muscle, in another muscle innervated by the same segment (L4/5) and in an area not supplied by the same segment (i.e. the ipsilateral posterior shoulder). In addition, this study will assess if functionality, as measured by the Oswestry Disability Index (ODI) and 15-point Global Rating of Change Scale (GRoC) questionnaires, improves after 2-3 treatments (1 week) of DN.

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