RecruitingNCT06863428
Mymobility Knee ROM
Concordance Between an App-based Range of Motion Measurement and Standard Goniometer.
Sponsor
Zimmer Biomet
Enrollment
41 participants
Start Date
Nov 21, 2025
Study Type
OBSERVATIONAL
Conditions
Summary
This prospective study aims to evaluate the agreement, also referred as concordance, of the mymobilty knee ROM with a clinician's assessment of knee ROM via goniometer.
Eligibility
Min Age: 18 Years
Inclusion Criteria2
- Patient is a minimum of 18 years of age
- Patient is willing and able to provide written Informed Consent by signing and dating the IRB-approved Informed Consent form
Exclusion Criteria3
- The patient is currently participating in any other study that would hinder the assessor's ability to measure knee ROM
- Complex primary knee pathology with significant restrictions on the range of motion per surgeon discretion
- Patient is pregnant or considered a member of a protected population (e.g. prisoner, mentally incompetent, etc.)
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Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06863428