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Clinical Trial Summary

the aim of the study is to determine whether a scapular strength exercise program combined with a conventional exercise program in epicondylar region in patients with lateral epicondylalgia produces statistically significant improvements in pain in the short and medium term compared to a conventional exercise program.


Clinical Trial Description

It is a single-blind clinical trial design, with third-party evaluation. There are two groups, the control group and the experimental group. In the control group, only the conventional exercise program for epicondylar muscles will be performed and the experimental group will also perform a scapular exercise program. Group assignment is randomized using the G* POWER software program, following the inclusion and exclusion criteria. Variables related to pain, functionality, pressure pain threshold, prehensile strength and quality of life will be measured. The study will last 7 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05373056
Study type Interventional
Source University of Alcala
Contact Alejandro AY Ayuso Pablo, Msc
Phone 647396334
Email aayusopablo@gmail.com
Status Recruiting
Phase N/A
Start date February 28, 2022
Completion date July 30, 2022

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