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Comparison of sensorimotor and supportive insoles for children with flat feet, to the use of a neutral insole - a randomized, prospective, controlled survey

Comparison of sensorimotor and supportive insoles for children with flat feet, to the use of a neutral insole - a randomized, prospective, controlled survey

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00035374
Enrollment
105
Registered
2024-12-03
Start date
2025-09-18
Completion date
Unknown
Last updated
2026-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Q66.6

Interventions

Group 1: Children who meet the criteria for the presence of a flexible flat foot and who have presented at the Clinic for Orthopaedics at the UKSH Lübeck during the designated study period will be exa
these are numbered consecutively from the outside and may only be opened once the person interested in the study has confirmed his participation. The envelope contains the questionnaires, the examinat
these are numbered consecutively from the outside and may only be opened once the person interested in the study has confirmed his participation. The envelope contain

Sponsors

Klinik für Orthopädie UKSH Lübeck
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 12 Years

Inclusion criteria

Inclusion criteria: - Children with a flexible flat foot - Children from 5 - 12 years - Boys and girls - Neuromotoric healthy children

Exclusion criteria

Exclusion criteria: - Rigid flat foot - Other structural foot deformities (congenital/acquired) - Neurological, genetic underlying diseases - Foot injury, foot surgery in the last 6 months - Lack of consent to participate

Design outcomes

Primary

MeasureTime frame
How effective is sensorimotor and supportive insole therapy compared to a neutral insole for children with flat feet? This question is to be answered on the basis of subjective patient satisfaction, using questionnaires (OxAFQ-C, AOFAS) and objective criteria (range of motion of the foot and ankle, standing on one leg, tiptoeing, FPI, pedobarography, muscle activity measurement using adhesive electrodes). After 3 months, only the questionnaires are sent to the test subjects. After 6 and 12 months, in addition to answering the questionnaires, the objective criteria (see above) are determined.

Secondary

MeasureTime frame
Determination of foot malposition, foot function and complaints in all three groups using: - OxAFQ-C - FPI - AOFAS (midfoot, hindfoot) - clinical examination - pedobarography - muscle activity measurement

Countries

Germany

Contacts

Public ContactMartin Russlies

Orthopädie, UKSH Lübeck

sarah.hardt@uksh.de+49 451-500 41109

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 28, 2026