Status:

COMPLETED

Dry Needling for Sub Acromial Pain Syndrome

Lead Sponsor:

59th Medical Wing

Conditions:

Subacromial Impingement Syndrome

Eligibility:

All Genders

18-65 years

Phase:

NA

Brief Summary

This trial will investigate the benefit of trigger point dry needling (DN) for individuals with a common cause of shoulder pain - sub-acromial pain syndrome. Sub-acromial pain syndrome, also knowns as...

Detailed Description

STUDY PURPOSE: The purpose of this study is to assess the long-term additive effectiveness of dry needling (DN) therapy to a standard physical therapy (PT) approach of manual therapy and exercise for...

Eligibility Criteria

Inclusion

  • Age 18 to 65
  • Read and speak English well enough to provide informed consent, follow study instructions, and independently answer the questionnaires/surveys
  • Tricare beneficiary
  • Primary complaint of new episode of shoulder pain; defined as not having sought care for shoulder condition in 6 months prior
  • Available and willing to come in for treatment (\~10 sessions over 6 week period)
  • Meets criteria for SAPS from description below, by having 2 of the 4 following physical exam findings:
  • Impingement signs (Neer, Hawkins, or Jobe tests)
  • Painful arc
  • Pain with isometric resistance (ER/IR/ABD)
  • Rotator cuff weakness on the injured side in comparison to the opposite side

Exclusion

  • History of shoulder dislocation, subluxation, fracture, adhesive capsulitis of the glenohumeral joint, or cervical/shoulder/upper back surgery
  • Presence of cervical radiculopathy, radiculitis, or referral from cervical spine
  • Total baseline SPADI score less than 20% (to prevent a ceiling effect with treatment)
  • Anyone pending a medical evaluation board, discharge from the military for medical reasons, or pending or undergoing any litigation for an injury
  • Unable to give informed consent to participate in the study.
  • Pregnancy

Key Trial Info

Start Date :

March 6 2018

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

August 20 2022

Estimated Enrollment :

121 Patients enrolled

Trial Details

Trial ID

NCT03442894

Start Date

March 6 2018

End Date

August 20 2022

Last Update

July 24 2025

Active Locations (1)

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Wilford Hall Ambulatory Surgical Center

San Antonio, Texas, United States, 78236