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Clinical Trial Summary

The purpose of this study is to ascertain whether 4 weeks of daily virtual-reality-based rehabilitation at home improves disability in the early stages of recovery from anterior cruciate ligament reconstruction surgery compared with standard care.


Clinical Trial Description

After being informed about the study and potential risks and benefits, patients giving written informed consent will be randomized to one of two groups in a 1:1 ratio. The treatment group will perform daily a 20-minute rehabilitation session in virtual reality, in which they will observe their virtual body performing a series of exercises they would otherwise be unable to perform in real life. Both groups will also undergo the standard rehabilitation protocol. The investigators will assess for differences between groups in self-reported disability, knee range of motion, and quadriceps strength at baseline, 4 weeks, 12 weeks and 9 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05080894
Study type Interventional
Source Institut d'Investigacions Biomèdiques August Pi i Sunyer
Contact
Status Completed
Phase N/A
Start date October 1, 2021
Completion date December 15, 2023

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