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Clinical Trials/NCT02338908
NCT02338908
Completed
Not Applicable

Effectiveness of Dry Needling and Eccentric Exercises in Unspecific Shoulder Pain

Universidad Rey Juan Carlos1 site in 1 country50 target enrollmentJanuary 2015
ConditionsShoulder Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Shoulder Pain
Sponsor
Universidad Rey Juan Carlos
Enrollment
50
Locations
1
Primary Endpoint
Changes in disability between baseline and follow-up periods
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Shoulder pain is highly prevalent in the society. The role of muscle tissues in this pathology has received increasing interest. Some studies have proposed the role of myofascial trigger points in this population. The purpose of the current clinical trial is to compare the effects of physiotherapy treatment consisting of an eccentric exercise protocol versus the same physical therapy program plus the addition of trigger point dry needling (TrP-DN) on pain and function in patients suffering from unspecific shoulder pain.

Registry
clinicaltrials.gov
Start Date
January 2015
End Date
March 2016
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

César Fernández-de-las-Peñas

Proffesor

Universidad Rey Juan Carlos

Eligibility Criteria

Inclusion Criteria

  • Unilateral non-traumatic shoulder pain
  • Shoulder pain from at least 3 months
  • Shoulder pain of more than 4 points on a NPRS

Exclusion Criteria

  • bilateral shoulder symptoms
  • younger than 18 or older than 65 years
  • history of shoulder fractures or dislocation
  • cervical radiculopathy
  • previous interventions with steroid injections
  • fibromyalgia syndrome
  • previous history of shoulder or neck surgery
  • any type of intervention for the neck-shoulder area during the previous year

Outcomes

Primary Outcomes

Changes in disability between baseline and follow-up periods

Time Frame: Baseline, one week after the last intervention and 3, 6 and 12 months after the intervention

The Disabilities of the Arm, Shoulder and Hand (DASH) will be used to determine the disability induced by shoulder pain

Secondary Outcomes

  • Changes in shoulder pain between baseline and follow-up periods(Baseline, one week after the last intervention and 3, 6 and 12 months after the intervention)

Study Sites (1)

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