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Clinical Trial Summary

The purpose of this study is to compare scapular muscle endurance (SME), shoulder pain, and functionality of patients with rotator cuff related shoulder pain (RCRSP) with those in the age-gender matched healthy controls and to evaluate the relationship between SME with shoulder pain, and functional impairments in patients with RCRSP.


Clinical Trial Description

Patients with RCRSP (n:23), and age-gender matched healthy controls (n:23) were included in the study. SME were measured by a one-kilogram dynamometer while the shoulder and elbows are flexed 90°. Self-reported pain intensity (activity, night, after SME and FIT-HaNSA) was assessed visual analog scale (VAS). Functionality was also assessed using the Functional Impairment test-hand, neck, shoulder, and arm (FIT-HaNSA). ;


Study Design


Related Conditions & MeSH terms

  • Rotator Cuff Syndrome of Shoulder and Allied Disorders
  • Shoulder Pain

NCT number NCT03651401
Study type Observational [Patient Registry]
Source Gazi University
Contact
Status Completed
Phase
Start date December 2015
Completion date January 2018

See also
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Completed NCT05516186 - Effects of a Scapular-focused Exercise Protocol N/A
Recruiting NCT06078865 - FX Shoulder Prospective Clinical Study
Terminated NCT03245320 - Clinical Evaluation of the TITAN™ Total Shoulder System
Not yet recruiting NCT06449534 - The Effect of the Treatment Environment on Pain, Function, Self Efficacy and Satisfaction in RCRSP N/A
Not yet recruiting NCT06435494 - Cross-sectorial Use of Patient-Reported Outcomes in Chronic Degenerative Shoulder Conditions N/A
Active, not recruiting NCT03167138 - Micro-Fragmented Adipose Tissue (Lipogems®) Injection for Chronic Shoulder Pain in Persons With Spinal Cord Injury Early Phase 1
Recruiting NCT06077942 - FX Shoulder Solutions Retrospective / Prospective Clinical Study
Withdrawn NCT04361266 - Use of Nanoscaffold Augmentation in Rotator Cuff Repair: Clinical Outcome and Ultrasound Assessment of Healing Rates and Vascularity N/A