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Clinical Trials/NCT02646306
NCT02646306
Completed
Not Applicable

A New Neurocognitive Interpretation of the Shoulder Position Sense During Reaching

University of Roma La Sapienza1 site in 1 country44 target enrollmentJuly 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Shoulder Impingement Syndrome
Sponsor
University of Roma La Sapienza
Enrollment
44
Locations
1
Primary Endpoint
Evaluation of the Visual Analogue Scale (VAS) at baseline
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The aim of the study focused on the creation of a rehabilitative measuring device (SRPT-shoulder proprioceptive rehabilitation tool) and the development of the examination methodology for assessing the proprioception of the glenohumeral joint respect to scapula abduction, within the movement of antepulsion on the sagittal plane both in healthy subjects and in patients with shoulder impingement syndrome.

Registry
clinicaltrials.gov
Start Date
July 2015
End Date
January 2016
Last Updated
10 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University of Roma La Sapienza
Responsible Party
Principal Investigator
Principal Investigator

Teresa Paolucci

Medical Director

University of Roma La Sapienza

Eligibility Criteria

Inclusion Criteria

  • Right-handed
  • Diagnosis of subacromial right impingement syndrome performed by the orthopedic specialist (nuclear magnetic resonance and/or ultrasound examination)
  • Neer stages 1, 2 and 3
  • Presence of pain 3 \<VAS\<8 at baseline
  • Age between 55 and 65 years.

Exclusion Criteria

  • Diabetes mellitus
  • Inflammatory systemic diseases
  • CNS and/or PNS diseases
  • Systemic infectious diseases
  • Neoplastic diseases
  • Assumption of antidepressants and/or anxiolytics and/or other medications that can affect attention and sensory
  • Visual problems not properly compensated
  • Previous surgery to the shoulder

Outcomes

Primary Outcomes

Evaluation of the Visual Analogue Scale (VAS) at baseline

Time Frame: baseline

It is an instrument that enables patients to express their pain intensity as a numerical value. Patients were asked to mark the point that corresponded to their perceived pain intensity on a 10-cm line, with 0 indicating the absence of pain and 10 reflecting the most severe pain

Secondary Outcomes

  • Evaluation of the short form of the Disabilities of the Arm, Shoulder and Hand questionnaire (Quick-DASH) at baseline(baseline)
  • Evaluation of the Constant-Murley shoulder outcome score at baseline(baseline)

Study Sites (1)

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