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Clinical Trial Summary

The purpose of this study is to verify the immediate effects of Tissue Flossing on knee flexion range of motion


Clinical Trial Description

After completing the questionnaire, 58 healthy participants will be randomly divided into two groups named Intervention Group (IG) (n=29) and Control Group (CG) (n=29). In the first assessment (M0), knee flexion ranges will be measured using a goniometer. Then the control group (n=29), without Tissue Flossing and intervention group (n=29) with Tissue Flossing around the knee joint will be subjected to passive and then active mobilization of the knee joint. Immediately after the intervention/control, the two groups will be assessed again (M1). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06205069
Study type Interventional
Source University Fernando Pessoa
Contact
Status Completed
Phase N/A
Start date February 15, 2024
Completion date March 29, 2024

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