Dry needling in addition to standard physical therapy treatment for sub-acromial pain syndrome: a randomized controlled trial protocol

Ben R Hando; Daniel I Rhon; Joshua A Cleland; Suzanne J Snodgrass

doi:10.1016/j.bjpt.2018.10.010

Dry needling in addition to standard physical therapy treatment for sub-acromial pain syndrome: a randomized controlled trial protocol

Braz J Phys Ther. 2019 Jul-Aug;23(4):355-363. doi: 10.1016/j.bjpt.2018.10.010. Epub 2018 Nov 6.

Authors

Ben R Hando¹, Daniel I Rhon², Joshua A Cleland³, Suzanne J Snodgrass⁴

Affiliations

¹ Wilford Hall Ambulatory Surgical Center, Joint Base San Antonio, Lackland, TX, United States; Discipline of Physiotherapy, The University of Newcastle, Callaghan, NSW, Australia. Electronic address: benjaminhando@gmail.com.
² Baylor University, Doctoral Program in Physical Therapy, Waco, TX, United States; Discipline of Physiotherapy, The University of Newcastle, Callaghan, NSW, Australia.
³ Department of Physical Therapy, Franklin Pierce University, Manchester, NH, United States.
⁴ Discipline of Physiotherapy, The University of Newcastle, Callaghan, NSW, Australia.

Abstract

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.

Keywords: Dry-needling; Manual therapy; Physical therapy; Shoulder pain; Subacromial impingement syndrome; Subacromial pain syndrome.

Publication types

Randomized Controlled Trial

MeSH terms

Acupuncture Therapy*
Exercise
Exercise Therapy / methods*
Humans
Outcome Assessment, Health Care
Pain Measurement
Physical Therapy Modalities
Shoulder Pain / physiopathology*
Trigger Points

Associated data

ClinicalTrials.gov/NCT03442894