ENDOprosthetic joint replacement – improving treatment by integrating Prehabilitation, Rehabilitation, Individualized Management and Educatio

Not Applicable

Recruiting

• Conditions: M16.0; M17.0; Primary coxarthrosis, bilateral; Primary gonarthrosis, bilateral

• Registration Number: DRKS00013521
• Lead Sponsor: Klinische StudieneinheitOrthopädische Klinik, Universität Würzburg

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2018-01-15
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Adult males and females (age = 18 years)
Established diagnosis of Osteoarthritis of the hip, knee or shoulder
Given medical indication for total joint replacement.

Exclusion Criteria

Acute (< 3 months) or non-consolidated fractures;
Planed implantation of a custom-made prosthesis

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Intraindividual development of osteoarthritis-associated health-limitations as measured by the WOMAC-Score before and 3/6/12 months after surgery

Secondary Outcome Measures

Name	Time	Method
- Patient Reported Outcome, quantified by standardized questionaires <br>- Type and frequency of perioperative untoward events<br>- Improvement of quality of life in everyday life (EuroQol, PID, LEFS, IPAQ, VAS, CES-D)<br>- Improvement of strength and flexibility/mobility (Chair-Rising-Test, 6-Minute Walk Test, Gait Speed, Short Physical Performance Battery)<br>- Grip strength with dynamometer<br>- Ground reaction force measurement (Leonardo plate) <br>- Body composition (Bioimpedance Analysis)<br>- Satisfaction with artificial joint