Knee Range of Motion
Conditions
Keywords
mymobility, range of motion, goniometer
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.
Interventions
None listed
Sponsors
Zimmer Biomet
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
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.)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 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. |
Countries
United States
Contacts
STUDY_DIRECTORHillary Overholser
Zimmer Biomet
Outcome results
None listed