Mymobility Knee ROM

Zimmer Biomet

Status: Enrolling

Conditions: Knee Range of Motion

Study type: Observational

Funder types: Industry

Identifiers

NCT06863428

CSU2024-28TDS

Details and patient eligibility

About

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.

Enrollment: 41 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

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.)

Trial design

41 participants in 1 patient group

Group 1

Description:

This group will have their knee range of motion measured three times. Once with the mymobility app, and twice using a goniometer by two separate assessors. Each assessor will be blinded to the other assessor's measurements.