Coordination and proprioception of the knee joint - validity and reliability of the Mr Cube measurement system

Coordination and proprioception of the knee joint - validity and reliability of the Mr Cube measurement system - Validity and reliability of the Mr Cube

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON39785

Enrollment

150

Registered

2013-04-10

Start date

2013-05-01

Completion date

Unknown

Last updated

2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ACL reconstruction knee osteoarthritis patellar tendinopathy

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients following ACL reconstruction: - Age 18-50 years; - ACL reconstruction was performed 8 weeks until 1 year previously.;Patients with patellar tendinopathy: - Age 18-50 years;Patients with knee osteoarthritis: - Age 50-75 years; - Diagnosed with knee osteoarthritis, based on clinical signs and radiographs.;Healthy subject group: - Age 18-75 years.

Exclusion criteria

Exclusion criteria: Patients following ACL reconstruction - Neurologic or neuromuscular disorder; - Other lower extremity injury or disease that might interfere with the measurements; - Unable to fill in the questionnaire in the Dutch language.;Patients with patellar tendinopathy - Neurologic or neuromuscular disorder; - Other lower extremity injury or disease that might interfere with the measurements; - Unable to fill in the questionnaire in the Dutch language.;Patients with knee osteoarthritis - Inflammatory polyarthritis; - Total hip arthroplasty; - Total knee arthroplasty at the other knee; Neurologic or neuromuscular disorder; - Other lower extremity injury or disease that might interfere with the measurements; - Dementia; - Unable to fill in the questionnaire in the Dutch language.;Healthy subject group - Inflammatory polyarthritis; - Hip and/or knee osteoarthritis; - Total hip and/or total knee arthroplasty; - Neurologic or neuromuscular disorder; - Other lower extremity injury or disease that might interfere with the measurements; - Dementia; - Unable to fill in the questionnaire in the Dutch language.

Design outcomes

Primary

Measure	Time frame
The objective of the present study is to determine validity, test-retest reliability and discriminant ability of the Mr Cube. The terms of study parameters/endpoints are not applicable in this type of research.	—

Secondary

Measure	Time frame
Not applicable.	—

Countries

Netherlands

Outcome results