Mymobility Knee ROM

Not yet recruiting

• Conditions: Knee Range of Motion

• Registration Number: NCT06863428
• Lead Sponsor: Zimmer Biomet

Brief 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.

Detailed Description

Not available

Study Timeline

• Status Verified: 2025-03
• Study First Submitted: 2025-03-03
• Study First Submitted QC: 2025-03-06
• Last Update Submitted: 2025-03-06
• Study First Posted: 2025-03-07
• Last Update Posted: 2025-03-07
• Study Start: 2025-05-01
• Primary Completion: 2025-11-01
• Study Completion: 2026-05-01

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 41

Inclusion Criteria

• 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 Criteria

• 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.)

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Active knee flexion	Day 1 (Single Visit)	Patients will be asked to sit in a chair to measure full active knee flexion.
Active knee extension	Day 1 (Single Visit)	Patients will be asked to sit in a chair to measure full active knee extension.
Passive knee extension with overpressure	Day 1 (Single Visit)	Patients will be asked to sit in a chair to measure full passive knee extension while applying overpressure on their knee with their hands.