Clinical Trials Directory

Trials / Unknown

UnknownNCT05232773

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

Status
Unknown
Phase
Study type
Observational
Enrollment
42 (estimated)
Sponsor
Campus Bio-Medico University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
PROCEDUREAssessmentEvaluation of clinical and kinematic parameters

Timeline

Start date
2022-01-31
Primary completion
2023-07-30
Completion
2023-07-30
First posted
2022-02-10
Last updated
2023-04-06

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT05232773. Inclusion in this directory is not an endorsement.