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Clinical Trial Summary

The goal of this clinical trial is to compare in participant population (patients with rotator cuff tendinopathy of the shoulder) the effect of a Global Postural Reeducation (GPR) program vs. a nonspecific therapeutic (aerobic) exercise program


Clinical Trial Description

Participants who meet the inclusion criteria will be randomly distributed between group 1 "GPR", group 2 "exercise", or group 3 "no physical therapy intervention". Group 1 participants will receive a physical therapy treatment using the GPR method for 6 weeks consisting of 1 weekly session lasting 40 min performing "frog on the ground" and "sitting" poses. Patients in this group will also perform self-postures at home daily for 10 minutes. Group 2 participants perform training for 6 weeks using non-specific aerobic exercise consisting of a daily 20-minute walk at a speed of 4-5 km/h. Group 3 participants will not receive any physical therapy treatment and will serve as a control group. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05613998
Study type Interventional
Source Universidad Francisco de Vitoria
Contact Javier Alvarez-González
Phone +34629483292
Email j.alvarezglez.prof@ufv.es
Status Recruiting
Phase N/A
Start date October 30, 2022
Completion date October 2023

See also
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