Lower extremity fractures prescribed partial weight bearing.
Conditions
Interventions
Group 1: The study has 2 arms.
The first arm includes healthy subjects, the second arm includes patients.
The study's objective is to test the measurement method on healthy volunteers first, and if th
Sponsors
Klinikum Stuttgart
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Inclusion criteria were sufficient upper-body coordination and strength to perform partial weight bearing with crutches and a minimum age of 18 years.
Exclusion criteria
Exclusion criteria: foot malformations, acute or chronic injuries or diseases, gait disorders due to muscle weakness, shoe sizes outside the measuring sole size (EU size 36–46), underweight (BMI 30.0) individuals.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| A measurement lasts for approximately 30 minutes. Running a course without and then with biofeedback is one type of measurement. The primary end point is the ending of the intervention group's run. This applies to both arms. | — |
Secondary
| Measure | Time frame |
|---|---|
| Only the second arm contains the secondary endpoint. It is defined as the primary endpoint's conclusion plus two years. Patients will be contacted for a final exam, which will serve as the secondary endpoint. Clinical indicators like pain and range of motion are noted. The second endpoint is the conclusion of this study. | — |
Countries
Germany
Contacts
Public ContactTobias Merkle
Klinikum Stuttart
Outcome results
None listed