Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Rotator Cuff Tear
Type
Interventional
Phase
Not Applicable
Design
Allocation: Non-RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: cross-sectional experimental multimodal (clinical, biomechanical, radiological) data collection with multiple conditions and a control groupMasking: None (Open Label)Masking Description: Blinding to the experimental condition is not possible because of the obvious differences between conditions (additional load). However, the person processing the data will be blinded to the condition.Primary Purpose: Diagnostic

Participation Requirements

Age
Between 45 years and 85 years
Gender
Both males and females

Description

This project is to test the overall hypothesis that rotator cuff tear affects glenohumeral translation and that this functional instability depends on additional load applied, on anatomical and morphological variations, and on type and severity of the injury. The study is to investigate the dose-res...

This project is to test the overall hypothesis that rotator cuff tear affects glenohumeral translation and that this functional instability depends on additional load applied, on anatomical and morphological variations, and on type and severity of the injury. The study is to investigate the dose-response relationship between load-induced muscle activation (liMA) and load-induced glenohumeral translation (liTr) in patients with rotator cuff tears and asymptomatic control subjects. Furthermore the study is to investigate the in vivo dose-response relationship between additional weight and glenohumeral translation, to understand the biological variation in liTr, the influence of disease pathology on the liTr, the potential compensation by muscle activation and muscle size, and the influence of liTr on patient outcomes. This study entails cross-sectional experimental multimodal (clinical, biomechanical, radiological) data collection with multiple conditions and a control group.

Tracking Information

NCT #
NCT04819724
Collaborators
Swiss National Science Foundation
Investigators
Principal Investigator: Annegret Mündermann, Prof. Dr. Department of Orthopaedics and Traumatology, University Hospital Basel