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Dry Needling and Exercises in Shoulder Pain

Not Applicable
Completed
Conditions
Shoulder Pain
Interventions
Other: exercise program
Other: TrP-DN
Registration Number
NCT02338908
Lead Sponsor
Universidad Rey Juan Carlos
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
50
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Control groupexercise programPatients will be asked to perform an eccentric loading exercise program for the shoulder musculature, particularly the supraspinatus and infraspinatus muscles, to be performed on an individual basis twice every day. The therapeutic protocol will be applied for 5 weeks.
Experimental groupexercise programPatients will be asked to perform an eccentric loading exercise program for the shoulder musculature, particularly the supraspinatus and infraspinatus muscles, to be performed on an individual basis twice every day. The therapeutic protocol will be applied for 5 weeks. In addition, within the second and fourth sessions, they will receive TrP-DN over active TrPs in the shoulder muscles
Experimental groupTrP-DNPatients will be asked to perform an eccentric loading exercise program for the shoulder musculature, particularly the supraspinatus and infraspinatus muscles, to be performed on an individual basis twice every day. The therapeutic protocol will be applied for 5 weeks. In addition, within the second and fourth sessions, they will receive TrP-DN over active TrPs in the shoulder muscles
Primary Outcome Measures
NameTimeMethod
Changes in disability between baseline and follow-up periodsBaseline, 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 Outcome Measures
NameTimeMethod
Changes in shoulder pain between baseline and follow-up periodsBaseline, one week after the last intervention and 3, 6 and 12 months after the intervention

A 10-point Numerical Pain Rating Scale (NPRS; 0: no pain, 10: maximum pain) will be used to assess the patients' current level of shoulder pain and the worst level of pain experienced in the preceding week in the shoulder area.

Trial Locations

Locations (1)

César Fernández-de-las-Peñas

🇪🇸

Alcorcon, Madrid, Spain

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