endoprosthetic
Conditions
Interventions
Group 1: As part of the study, a digital system is being developed that supports patients in carrying out selected physiotherapeutic exercises by specifying a reference movement and analyzing the exec
Sponsors
Ostfalia Hochschule für angewandte Wissenschaften
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with upcoming or already completed hip or knee replacement
Exclusion criteria
Exclusion criteria: Subjects: existing skeletal disease, pain in the back or lower extremities as well as serious illnesses with associated reduced general condition. Patients: Patients who received both a hip and a knee implant at the same time or within a very short space of time as well as patients in whom special complications are to be expected or have already occurred are excluded. In addition, persons incapable of giving consent are excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Agreement between patients identified by the system who are recommended to be re-presented in the clinic and patients identified manually by physicians or physiotherapists using the target variables sensitivity, specification and AUROC | — |
Secondary
| Measure | Time frame |
|---|---|
| - User satisfaction with the system based on a suitable scale (e.g. uMARS) - qualitative agreement of the corrections and movement sequences suggested by the system with the corrections suggested by physiotherapists | — |
Countries
Germany
Contacts
Public ContactCarsten Meyer
Ostfalia Hochschule für angewandte Wissenschaften
Outcome results
None listed