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

Sponsor
Polytechnic Institute of Porto (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05814978
Collaborator
School of Health of Polytechnic Institute of Porto (Other), Center for Rehabilitation Research - Human Movement System (Re)habilitation Area (Other), Research Centre in Physical Activity, Health and Leisure, Faculty of Sport, University of Porto (Other), Porto Biomechanics Laboratory (Other), Center for Interdisciplinary Applied Research in Health, Health School of the Setubal, Polytechnic Institute (Other)
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Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Experimental Scapular Therapeutic Exercise Group
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effects of Scapular Therapeutic Exercise on Essential Biomechanical and Neurophysiological Parameters in Shoulder Pain Conditions With Scapular Impairments
Actual Study Start Date :
Mar 27, 2023
Anticipated Primary Completion Date :
Jul 1, 2023
Anticipated Study Completion Date :
Jul 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental Scapular Therapeutic Exercise Group

Patients in this group will perform therapeutic exercises, recommended for subjects with shoulder pain and focusing the neuromuscular control, stretching and/or strengthening of the scapular muscles

Other: Experimental Scapular Therapeutic Exercise Group
All subjects will perform a program of scapular therapeutic exercises including: neuromuscular control/strength - scapular therapeutic exercises that leads to, at least, moderate muscular activity levels; and stretching exercises. The intervention period will be of 8 weeks, considering in-person and/or home sessions.

Outcome Measures

Primary Outcome Measures

  1. Change in shoulder pain [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)

  2. Change in shoulder function [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).

  3. Change in scapular muscles activity levels [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

  4. Change in scapular muscles ratio [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.

  5. Change in kinematics [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 (°)

  6. Change in movement quality through time variables [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

  7. Change in movement quality through trunk compensation [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

  8. Change in movement quality through smoothness [Baseline and one week after intervention]

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

Secondary Outcome Measures

  1. Change in muscle stiffness [Baseline and one week after intervention]

    Scapular muscles stiffness will be assessed by myotonometry (using a digital palpation device)

  2. Change in pressure pain threshold [Baseline and one week after intervention]

    An assessment point in the shoulder area will be assessed by the application of a mechanical pressure by an algometer

  3. Change in pain-related fear [Baseline and one week after intervention]

    Assessed with self-reported scales - Tampa Scale for Kinesiophobia, which ranges from 13 (best) to 52 (worst)

  4. Change in pain catastrophization [Baseline and one week after intervention]

    Assessed with a self-reported scale - Pain Catastrophizing Scale, which ranges from 0 (better) to 52 (worst)

  5. Self-impression of change [One week after intervention]

    The patient's individual perspective about his/her condition and changes felt considering the intervention received will be assessed by a self-reported scale - Patient global impression of change scale, which range from 0 [no change (or condition has got worse)] to 7 (a great deal better, and a considerable improvement that has made all the difference)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Center for Rehabilitation Research, School of Health, Polytechnic of Porto Porto Portugal 4200 - 072

Sponsors and Collaborators

  • Polytechnic Institute of Porto
  • School of Health of Polytechnic Institute of Porto
  • Center for Rehabilitation Research - Human Movement System (Re)habilitation Area
  • Research Centre in Physical Activity, Health and Leisure, Faculty of Sport, University of Porto
  • Porto Biomechanics Laboratory
  • Center for Interdisciplinary Applied Research in Health, Health School of the Setubal, Polytechnic Institute

Investigators

  • Principal Investigator: Ana Melo, Polytechnic Institute of Porto

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ana Melo, Principal Investigator - PhD grant student, Polytechnic Institute of Porto
ClinicalTrials.gov Identifier:
NCT05814978
Other Study ID Numbers:
  • CE0108C
  • SFRH/BD/140874/2018
  • UIDB/05210/2020
First Posted:
Apr 18, 2023
Last Update Posted:
Apr 19, 2023
Last Verified:
Apr 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ana Melo, Principal Investigator - PhD grant student, Polytechnic Institute of Porto
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 19, 2023