Dry needling in addition to standard physical therapy treatment for sub-acromial pain syndrome: a randomized controlled trial protocol
| Autor: | Joshua A. Cleland, Suzanne J. Snodgrass, Daniel I. Rhon, Ben R. Hando |
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| Rok vydání: | 2018 |
| Předmět: |
medicine.medical_specialty
Clinical Trial Protocol Psychological intervention Acupuncture Therapy Physical Therapy Sports Therapy and Rehabilitation law.invention 03 medical and health sciences 0302 clinical medicine Randomized controlled trial law Shoulder Pain Outcome Assessment Health Care medicine Humans Orthopedics and Sports Medicine Exercise Physical Therapy Modalities Pain Measurement Protocol (science) 030222 orthopedics Dry needling Pain syndrome business.industry Rehabilitation Consolidated Standards of Reporting Trials Trigger Points Exercise Therapy Physical therapy Observational study Manual therapy business 030217 neurology & neurosurgery |
| Zdroj: | Brazilian journal of physical therapy. 23(4) |
| ISSN: | 1809-9246 |
| Popis: | Background Trigger point dry needling interventions are utilized by physical therapists to manage shoulder pain. Observational studies have shown positive short-term outcomes in patients with subacromial pain syndrome receiving trigger point dry needling. However, little research has been done to evaluate the long-term effectiveness of trigger point dry needling specifically as it compares to other commonly utilized interventions such as exercise and manual therapy. The purpose of this study is to assess the additive short and long-term effectiveness of trigger point dry needling to a standard physical therapy approach of manual therapy and exercise for patients with subacromial pain syndrome. Methods This multicenter randomized trial with 3 arms was designed following the standard protocol items for randomized interventional trials. Results will be reported consistent with the consolidated standards of reporting trials guidelines. 130 participants will be randomized to receive standard PT interventions alone (manual therapy and exercise), standard PT and trigger point dry needling or standard PT and sham trigger point dry needling. The primary outcome measures will be the Shoulder Pain and Disability Index and Patient Reported Outcomes Measurement Information Systems (PROMIS-57) scores collected at baseline, 6-weeks, 6-months and one year. Healthcare utilization will be collected for 12 months following enrollment and groups analyzed for differences. Discussion It is not known if trigger point dry needling provides long-term benefit for individuals with subacromial pain syndrome. This study will help determine if this intervention provides additive benefits over those observed with the commonly applied interventions of exercise and manual therapy. Trial registration Identifier: NCT03442894 ( https://clinicaltrials.gov/ct2/show/NCT03442894 ) on 22 February 2018. |
| Databáze: | OpenAIRE |
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