Prehabilitation for patients with osteoarthritis of the hip or knee waiting for a total Joint replacement for hip or knee

Not Applicable

Recruiting

• Conditions: M16; M17; Coxarthrosis [arthrosis of hip]; Gonarthrosis [arthrosis of knee]

• Registration Number: DRKS00009239
• Lead Sponsor: Orthopädische Praxis Großhansdorf

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2015-10-14
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

osteoarthritis of the hip or knee

Exclusion Criteria

Alzheimer's disease, dementia, disability to speak and understand German, serious neurological disorders, disability to walk at least 3 m

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The knee and hip patients as well as the patients with and without training programme estimate their pain using the VAS before the intervention (and the beginning of the training programme) (t = 0), after the end of the training programme (t = 1) and after 6 weeks, 3 months and 6 months (t = 2, 3, 4) postal-surgically.<br>Two primary hypotheses are examined: comparison of the mean change of the pain sensation (t = 0 to t = 2) in the therapy (VAS20t) and the control group (VAS20k) for patients with hip TJR and for patients with knee TJR: <br>null hypothesis (H0): VAS20t = VAS20k <br>alternative hypothesis (H1): VAS20t ? VAS20k <br>

Secondary Outcome Measures

Name	Time	Method
Besides of the comparison of the pain reductions in two groups, the following research questions are examined: <br>1) Development of the values VAS (estimation of pain) over the time <br>2) Development of the ROM values (mobility of knee (extension und flexion) and hip (extension, flexion and abduction))<br>3) Investigation of the values of KOOS (questionnaire of knee specific quality of life), HOOS (questionnaire of hip specific quality of life), SF-36 (questionnaire of general quality of life), timed-up-and-go-test (mobility), chair stand test (strength of the legs) and 40 m (speed test) and 6 min walking tests (walking endurance)<br><br>Assessments are conducted before (t=0) and after ((t=1) the programme and 6 weeks (t=2), 3 (t=3) and 6 (t=4) months after surgery.