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

Completed

• Conditions: ACL reconstruction; knee osteoarthritis; patellar tendinopathy; 10043237

• Registration Number: NL-OMON39785
• Lead Sponsor: niversitair Medisch Centrum Groningen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 150

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

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.

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The objective of the present study is to determine validity, test-retest<br /><br>reliability and discriminant ability of the Mr Cube. The terms of study<br /><br>parameters/endpoints are not applicable in this type of research.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Not applicable.</p><br>