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Effectiveness of a Group Intervention for the Treatment of Shoulder Pathologies

Not Applicable
Completed
Conditions
Shoulder Pain
Interventions
Procedure: Physiotherapy exercises guideline
Registration Number
NCT02541279
Lead Sponsor
Universidad Miguel Hernandez de Elche
Brief Summary

The investigators determined the effectiveness of a group intervention for the treatment of shoulder pathologies.

Detailed Description

The investigators performed a two-armed prospective clinical trial study, analyzing a sample formed by 76 patients with shoulder pain. The patients were allocated to one group randomly (intervention or control group). The data was obtained in the San Juan de Alicante Hospital between November 2014 and July 2015.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
76
Inclusion Criteria

-Patients who came to the Rehabilitation Service of the San Juan de Alicante Hospital between November 2014 and July 2015 with one of the diagnosed diseases indicated in the 726.10 ICD-9-CM code (nontraumatic rotator cuff tear, bursitis, tendinitis, and medical diagnostics impingement syndrome of any severity depending stadiums Neer (1990) unilateral or bilateral joint balance with free or minimally limited internal rotation).

Exclusion Criteria
  • Patients who cannot perform the exercises correctly (example: psychiatry disorders)
  • Patients with Shoulder surgery
  • Patients whose shoulder pain is above 7 according VAS pain.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InterventionPhysiotherapy exercises guidelineThe intervention group received 6 sessions of shoulder exercises controlled by a physiotherapist.
ControlPhysiotherapy exercises guidelineThe control group received a paper explaining the same exercises which were performed by the intervention group. This group made the exercises at home.
Primary Outcome Measures
NameTimeMethod
Constant Murley Testbefore/after intervention ( 6 weeks)

This test assesses daily activities.

Secondary Outcome Measures
NameTimeMethod
Quick-DASH Testbefore/after intervention ( 6 weeks)

This test assesses functional limitation in upper limb musculoskeletal disorders.

Pain NRS (numeric rating scale)before/after intervention ( 6 weeks)

Instruct the patient to choose a number from 0 to 10 that best describes their current pain. 0 would mean 'No pain' and 10 would mean 'Worst possible pain'

Measurement of the average forcebefore/after intervention ( 6 weeks)

Average force: Measurement was assessed in newtons

Trial Locations

Locations (1)

Miguel Hernández de Elche

🇪🇸

San Juan, Alicante, Spain

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