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Clinical Trials/NCT05814978
NCT05814978
Completed
Not Applicable

Effects of Scapular Therapeutic Exercise on Essential Biomechanical and Neurophysiological Parameters in Shoulder Pain Conditions With Scapular Impairments

Polytechnic Institute of Porto1 site in 1 country20 target enrollmentApril 20, 2023
ConditionsShoulder Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Shoulder Pain
Sponsor
Polytechnic Institute of Porto
Enrollment
20
Locations
1
Primary Endpoint
Change in shoulder pain
Status
Completed
Last Updated
last year

Overview

Brief Summary

Shoulder pain is a prevalent and recurrent condition. After a period of shoulder pain, some adaptations could be found, as in scapular muscles and kinematics and/or in nervous system.

It seems important to assess several biomechanical and neurophysiological outcomes to better characterize shoulder pain conditions and to program an intervention plane.

Therapeutic exercise is one of the treatments used for shoulder pain, however there are still doubts and controversial findings regarding exercise focusing the scapular musculature. Thus, the present study aims to assess the effects of an intervention protocol based on scapular therapeutic exercise.

Detailed Description

The study only started after approval of the protocol

Registry
clinicaltrials.gov
Start Date
April 20, 2023
End Date
August 31, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Polytechnic Institute of Porto
Responsible Party
Principal Investigator
Principal Investigator

Ana Melo

Principal Investigator - PhD grant student

Polytechnic Institute of Porto

Eligibility Criteria

Inclusion Criteria

  • 18 to 65 years old
  • Chronic (more than 3 months), continuously or intermittently, non-specific or associated with a diagnostic (except if mentioned in the exclusion criteria) shoulder pain of, at least, moderate intensity
  • Presenting scapular alterations as scapular dyskinesis (identified at rest or during motion)

Exclusion Criteria

  • History of shoulder fracture, dislocation, tears, infection or neoplasm
  • Shoulder surgery
  • Cervical and/or thoracic pathologies or pain associated with active movements of these regions
  • Neurological disease
  • Body mass index out of the range 18,5-30 kg/m2 and muscular skinfold higher than 20mm
  • Inability to perform the exercises
  • Current practice of competitive/high-level exercise/sport focusing the upper limb

Outcomes

Primary Outcomes

Change in shoulder pain

Time Frame: Baseline and one week after intervention

The intensity of pain will be measured with a self-reported 11-point scale (Numerical Rating Pain Scale), with scores ranging from 0 (no pain) to 10 (maximum pain)

Change in movement quality through time variables

Time Frame: Baseline and one week after intervention

Movement quality will be assessed considering time to peak acceleration and task completion time, calculated according to the data recorded with inertial sensors

Change in kinematics

Time Frame: Baseline and one week after intervention

Scapular kinematics and scapulohumeral rhythm, during shoulder analytical movements and during a functional task, will be measured by inertial sensors and described in degrees (°)

Change in movement quality through smoothness

Time Frame: Baseline and one week after intervention

Smoothness will be calculated by jerk logarithm of data recorded with inertial sensors

Change in shoulder function

Time Frame: Baseline and one week after intervention

Shoulder functional status will be measured with a self-reported 13 items scale (SPADI), which ranges from 0 (fully functional) to 100 (maximum degree of disability).

Change in scapular muscles activity levels

Time Frame: Baseline and one week after intervention

Scapular muscles activity levels, during shoulder analytical movements and during a functional task, will be recorded superficially by a wireless electromyographic signal detector system

Change in movement quality through trunk compensation

Time Frame: Baseline and one week after intervention

Movement quality will be also assessed considering the trunk motion, calculated according to the data recorded with inertial sensors

Change in scapular muscles ratio

Time Frame: Baseline and one week after intervention

Ratio between scapular muscles activity levels, during shoulder analytical movements and during a functional task, will be calculated considered the superficially eletromyographic data measured by a wireless electromyographic signal detector system.

Secondary Outcomes

  • Change in pain-related fear(Baseline and one week after intervention)
  • Change in muscle stiffness(Baseline and one week after intervention)
  • Change in pressure pain threshold(Baseline and one week after intervention)
  • Self-impression of change(One week after intervention)
  • Change in pain catastrophization(Baseline and one week after intervention)

Study Sites (1)

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