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Clinical Trials/ACTRN12624000798561
ACTRN12624000798561
Not yet recruiting
未知

Comparison of the effectiveness of an individualized exercise program in overhead sports athletes with symptoms of unilateral shoulder impingement syndrome: a randomized clinical trial.

niversidad Europea de Madrid0 sites40 target enrollmentJune 27, 2024

Overview

Phase
未知
Intervention
Not specified
Conditions
Shoulder impingement
Sponsor
niversidad Europea de Madrid
Enrollment
40
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 27, 2024
End Date
TBD
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversidad Europea de Madrid

Eligibility Criteria

Inclusion Criteria

  • Men and women.
  • \- Between 18\-40 years.
  • \- Shoulder pain lasting at least 3 months.
  • \- At least 2 positive tests out of 5, according to the diagnostic criteria for shoulder impingement
  • \- Subjects who practice CrossFit®.

Exclusion Criteria

  • \- History of surgical interventions (History of fracture of the clavicle, scapula and/or humerus; glenohumeral arthritis; inflammatory arthritis; adhesive capsulitis), congenital disorders already diagnosed that may affect the shoulder joint complex, rotator cuff tendinopathy, partial\-total tears of the rotator cuff and signs of glenohumeral instability.
  • \- Currently carrying out physiotherapy treatment.
  • \- Evidence of structural injury in structures of the shoulder joint complex and in tendon structures such as partial or complete ruptures of rotator cuff tendons.
  • \- Metabolic, neurological, autoimmune or cardiovascular diseases that may affect the shoulder region.
  • \- Inability to understand the oral and written language of the study protocol, as well as cognitive disorders.
  • \- Taking analgesic or anti\-inflammatory medication a week prior to the measurement or during the intervention.
  • \- Participants who present a moderate\-intense level of physical activity according to the IPAQ questionnaire.

Outcomes

Primary Outcomes

Not specified

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