Q66.6
Conditions
Interventions
Group 1: After a physician diagnoses pes planovalgus, the patient is referred to a medical supply store for orthotic treatment based on the doctor’s recommendation. The type of treatment is determined
Sponsors
RPTU Kaiserslautern - Landau
Eligibility
Sex/Gender
All
Age
6 Years to 17 Years
Inclusion criteria
Inclusion criteria: Pes planovalgus
Exclusion criteria
Exclusion criteria: - All diseases potentially affecting sensorimotor control (e.g. diabetes mellitus, neurological disorders). - No acute injury potentially effecting habitual walking was al-lowed. - Children with previous experience wearing foot orthoses were not included.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The endpoint for all participants is the 4-week intervention period (T3, shoes + foot orthoses). However, baseline (T1; only shoes) and immediate (T2, shoes + foot orthoses) measurements must first be taken on the first day of treatment. At all test time points, only the hindfoot angle is measured. Consequently, at the end of the study, the hindfoot angles at T1, T2, and T3 are available for the randomly assigned treatment (SMFO or BMFO). | — |
Countries
Germany
Contacts
Public ContactStephan Becker
RPTU Kaiserslautern - Landau
Outcome results
None listed