Effectiveness of a Group Intervention for the Treatment of Shoulder Pathologies
- 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
-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).
- 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
Group Intervention Description Intervention Physiotherapy exercises guideline The intervention group received 6 sessions of shoulder exercises controlled by a physiotherapist. Control Physiotherapy exercises guideline The 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
Name Time Method Constant Murley Test before/after intervention ( 6 weeks) This test assesses daily activities.
- Secondary Outcome Measures
Name Time Method Quick-DASH Test before/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 force before/after intervention ( 6 weeks) Average force: Measurement was assessed in newtons
Trial Locations
- Locations (1)
Miguel Hernández de Elche
🇪🇸San Juan, Alicante, Spain