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Clinical Trial Summary

The objective of the study is to analyze whether observing the actions of a referent selected by the participants improves balance in asymptomatic individuals compared to those who observe a standard referent.


Clinical Trial Description

Design: Randomized controlled clinical trial. The primary endpoint of the study was the balance recorded by force platform (estatic) and Y balance test (dynamic). Setting: The participants will be healthy people in the province of Tarragona. Participants: They will be randomly assigned to one of three groups using a computerized randomized list: - Control Group (CG): Participants will watch a video of landscapes without human or animal movement. - Intervention Group with Referent (GIR): Participants will observe actions whose referent has been selected by themselves based on perceived similarity. - Standard Intervention Group (GIE): Participants will observe actions with a standard reference. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06206668
Study type Interventional
Source University Rovira i Virgili
Contact Tania López Hernández
Phone +34620438175
Email tania.lopez@urv.cat
Status Not yet recruiting
Phase N/A
Start date February 1, 2024
Completion date December 30, 2024

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