Test re-test reliability of a Functional Capacity Evaluation in an early osteoarthritis cohort

Completed

• Conditions: functional capacity; osteo-arthritis; 10023213

• Registration Number: NL-OMON31797
• Lead Sponsor: niversitair Medisch Centrum Groningen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 13 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 30

Inclusion Criteria

• Age: 45 -65 years
• Pain and / or stiffness of hip and / or knee

Exclusion Criteria

• Patients with inflammatory rheumatic diseases like rheumatoid arthritis and spondylitis ankylopoetica
• Patients with osteoarthritis Kellgren IV in one or more of the four joints (hips end knees)
• Patients with prostheses in one of the four joints
• Patients with serious comorbidity that makes physical assessment difficult or impossible or results in a much shorter life expectancy
• Patients who have had a tumour in the last 5 years (except for skin carcinomas without metastases)
• Patients who do not understand the dutch language in such a way that questionnaires can be filled in
• Patients who only have symptoms of local tendinitis and / or bursitis
• Patients with acute pain after a trauma or an accident
• Patients with radiculating pain in the knee and / or hip region

Study & Design

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

Primary Outcome Measures

Name	Time	Method
<p>Primary study parameters are the results on the items of the FCE. These are<br /><br>expressed in kilogrammes, newtons and seconds.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>not applicable</p><br>