Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ENROLLING_BY_INVITATION
400 participants
OBSERVATIONAL
2024-04-01
2027-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Total Knee Arthroplasty
Patients receiving a total knee arthroplasty
Return to Activity Battery
The main target parameters are muscle mass (sonography), muscle strength (isometric maximum strength measurement), neuromuscular activation (surface EMG), functionality (e.g. 6MWT, chair rising test), knee swelling and subjective assessment of everyday and leisure activities, quality of life (e.g. SF-36) and return to work
Interventions
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Return to Activity Battery
The main target parameters are muscle mass (sonography), muscle strength (isometric maximum strength measurement), neuromuscular activation (surface EMG), functionality (e.g. 6MWT, chair rising test), knee swelling and subjective assessment of everyday and leisure activities, quality of life (e.g. SF-36) and return to work
Eligibility Criteria
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Inclusion Criteria
* Ability to perform the return to activity battery
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University Hospital, Bonn
OTHER
Responsible Party
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Alexander Franz
Dr. med., B.Sc.
Locations
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Technical University Munich
Munich, Bavaria, Germany
University Hospital Bonn
Bonn, North Rhine-Westphalia, Germany
Countries
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Other Identifiers
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2024_I
Identifier Type: -
Identifier Source: org_study_id
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