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Scientific accompanying evaluation of an innovative process chain to ensure work ability after total joint replacement

Not Applicable
Recruiting
Conditions
M16
M17
Z96.6
Z96.8
Coxarthrosis [arthrosis of hip]
Gonarthrosis [arthrosis of knee]
Presence of orthopaedic joint implants
Presence of other specified functional implants
Registration Number
DRKS00029630
Lead Sponsor
Deutsche Rentenversicherung Rheinland
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
845
Inclusion Criteria

First implantation of a total hip or knee arthroplasty due to chronic degenerative joint disease (ICD-10: M 16 & M 17 [Z 96.6 & Z 96.8]),
- employment,
- Insurance at a regional institution of the German Pension Insurance and
- Fulfilment of the insurance requirements for follow-up treatment.

Exclusion Criteria

- total arthroplasty replacement and
- total arthroplasty after accident/acute trauma

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Outcome evaluation: functionality at work (scales for assessing functionality at work (SE-FFB); Mueller et al., 2014); time points: preoperative (baseline), 12, 24, and 48 weeks after the start of rehabilitation.
Secondary Outcome Measures
NameTimeMethod
- Outcome evaluation: activities, participation<br>- Process evaluation: Complications in the course of rehabilitation, acceptance, satisfaction, and feasibility of the process chain from different perspectives (quantitative questionnaires and qualitative guided interviews and focus groups with patients, doctors, therapists, social services, funders)<br>
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