Pain, Shoulder Pain, Scapular, Abdominal Muscles
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Both sexes; have a medical or physiotherapeutic diagnosis of subacromial pain; positivity in specific orthopedic tests (Neer, Hawkins-Kennedy, Jobe and painful arch); be physically independent.
Exclusion criteria
Exclusion criteria: Present clinical conditions or unstable disease that contraindicates the practice of supervised physical exercise; present range of motion of arm flexion less than 120°; have a history of trauma or surgery on the shoulder; have severe deformities in the thoracic spine (scoliosis or hyperkyphosis); be positive for clinical tests of glenohumeral instability.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of scapular kinematics (in degrees) obtained through isoinertial sensors. This assessment will be carried out at the beginning (before randomization) and at the end (after 8 weeks) of the intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain and disability assessment (score) obtained through the SPADI questionnaire. This assessment will be performed at the beginning (before randomization) and at the end (after 8 weeks) of the intervention.;Assessment of muscle strength and power of the shoulder's internal and external rotators (in N/m and Watts) obtained using an isokinetic dynamometer. This assessment will be performed at the beginning (before randomization) and at the end (after 8 weeks) of the intervention.;Assessment of upper limb stability (in touch per second) obtained through the Closed Kinetic Chain Upper Extremity Stability test. This assessment will be performed at the beginning (before randomization) and at the end (after 8 weeks) of the intervention.;Assessment of scapular positioning (in centimeters) obtained through the length of the pectoralis minor muscle and the shoulder-table distance. This assessment will be performed at the beginning (before randomization) and at the end (after 8 weeks) of the intervention.;Assessment of glenohumeral internal rotation deficit (in degrees) obtained through goniometry. This assessment will be performed at the beginning (before randomization) and at the end (after 8 weeks) of the intervention.;Evaluation of the isometric resistance of the trunk (in seconds) obtained by means of a stopwatch. This assessment will be performed at the beginning (before randomization) and at the end (after 8 weeks) of the intervention. | — |
Countries
Brazil