Q66.5
Conditions
Interventions
Group 1: Therapy group 1: supportive insole
Group 2: Therapy group 2: sensorimotor insole
Group 3: Control group: Placebo insole
Sponsors
Klinik und Poliklinik für Orthopädie, Universitätsmedizin Rostock
Eligibility
Sex/Gender
All
Age
6 Years to 16 Years
Inclusion criteria
Inclusion criteria: patients with flat foot agreement to participate in the study readiness for follow up examinations Age from 6 until 16 Years
Exclusion criteria
Exclusion criteria: - Inability to recognize the scope of therapy - Lack of willingness to wear insoles - Lack of consent - Rheumatic disease - Neuropathy of any genesis - Acute trauma - High arch - Rigid flat foot - Structural deformity of the lower extremity
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The aim is to compare the muscle activation of the lower leg muscles by the insoles. For this purpose, a surface EMG of the lower leg musculature is performed at the time of recruitment, after 6 and after 12 months, the measurement is performed at all time points barefoot, in the shoe and in the shoe with insole. | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation of clinical effects using the footprint, valgus index, pain level on a VAS, and questionnaire (FADI). | — |
Countries
Germany
Contacts
Public ContactKira-Henriette Liebau
Klinik und Poliklinik für Orthopädie, Universitätsmedizin Rostock
Outcome results
None listed