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Rotator Cuff Surgery in Athletes: From Rehabilitation to Return to Sport — RCR-SPORT  

Rotator Cuff Tears Clinical Trial

Official title:
Rotator Cuff Surgery in Athletes: From Rehabilitation to Return to Sport

Clinical Trial Summary

The main goal of this project is to study and define a rehabilitative flow-chart for athletes' rehabilitation and return to sport made by a set of objective shoulder evaluation indicators that are easy to use in clinical context. Enrolled patients will undergo supervised rehabilitation treatment for rotator cuff repair according to a standardized protocol (5 days/week) and will undergo four evaluation at different times. Healthy subjects will undergo evaluations with the same timing as patients.

Clinical Trial Description

Clinical, kinematic and shoulder muscle strength assessments to collect data useful to define objective criteria for progression between rehabilitation phases will be performed according to the following times: - T1 - 4-6 weeks after surgery: PROM assessment, pain assessment at rest and during PROM, Constant-Murley score (CMS). - T2 - 6-12 weeks after surgery: AROM assessment (flexion in scapular plane, abduction, external and internal rotation), pain assessment at rest and during PROM and AROM tasks, scapular humeral rhythm, CMS. - T3 - 12-16 weeks after surgery: AROM assessment (flexion in scapular plane, abduction, external and internal rotation), pain assessment at rest and during PROM and AROM tasks, scapular humeral rhythm, isometric strength assessment, CMS; joint proprioception assessment (joint position sense). - T4 - 16-24 weeks after surgery: AROM assessment (flexion in scapular plane, abduction, external and internal rotation), scapular humeral rhythm, isometric strength assessment, CMS, joint proprioception assessment (joint position sense), movement speed and smoothness. Enrolled patients will undergo supervised rehabilitation treatment for rotator cuff repair according to a standardized protocol (5 days/week) and will undergo the evaluations. Healthy subjects will undergo evaluations with the same timing as patients. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05232773
Study type Observational
Source Campus Bio-Medico University
Contact Marco Bravi, Dott.
Phone 0622541624
Email m.bravi@policlinicocampus.it
Status Recruiting
Phase
Start date January 31, 2022
Completion date July 30, 2023
View Details
See also
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