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Measurement of the Strength of the Posterior Tibial Muscle by Hand-held Dynamometer

Validation of the Measurement of the Strength of the Posterior Tibial Muscle by Hand-held Dynamometer Against a Reference Isokinetic Dynamometer

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04673669
Acronym
TPHHD
Enrollment
46
Registered
2020-12-17
Start date
2021-03-23
Completion date
2022-03-11
Last updated
2025-12-23

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

Conditions

Valgus Foot Deformity

Keywords

Posterior tibial, hand-held dynamometer, isokinetics, isokinetics, measurement validation

Brief summary

Adult flat foot valgus is a degenerative pathology that causes damage to the ligaments of the hindfoot as well as dysfunction of the tendon of the posterior tibial muscle. Currently, there is a lack of a tool allowing a standardized, reliable, reproducible and validated measurement of the strength of the tendon of the posterior tibial muscle in consultation of foot surgery. The hand-held dynamometer could be that tool. The study would consist in measuring the strength of the tendon of the posterior tibial muscle in healthy subjects with a hand-held dynamometer (MicroFET2) by two examiners and compared to isometric reference measurements (CON-TREX CMV Multi-Joint) to validate the reliability of the measurement and its reproducibility.

Interventions

DIAGNOSTIC_TESTPosterior tibial tendon strength mesure

Posterior tibial tendon strength is assessed with a hand-held dynamometer by two independent observer and with an isometric dynamometer by one observer.

Sponsors

University Hospital, Lille
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients from physical medicine and rehabilitation department hospitalized for pathologies other than neurological or osteo-articular pathologies affecting the lower limbs, * Having no neurological or osteo-articular pathology affecting the lower limbs f one year, * No history of surgery on the rear foot and ankle, * Written informed consent from person, * Socially insured patient person, * Person willing to comply with all study procedures and study duration.

Exclusion criteria

* Neurological or osteo-articular pathologies affecting the lower limbs, * Known pathologies of the tendon of the posterior tibialis muscle, * Deformations of the foot (flat foot, hollow foot), * History of hindfoot or ankle surgery, * Pregnant or breastfeeding woman, * Inability to receive information, consent and participate in the whole study, * Person under judicial protection or deprived of liberty, * Person participating in another clinical trial, * No social insurance cover, * No written consent.

Design outcomes

Primary

MeasureTime frameDescription
Intra-class correlation coefficient of the inversion force (or supination measured in Newton) of the foot between the measurement made with the hand dynamometer and the measurement made with the isokinetic dynamometer (gold standard).on the day of first evaluation (at day 1)Validity of the measurement of the tendon strength of the posterior tibial muscle with a hand-held dynamometer (MicroFET2) compared to the gold standard (CON-TREX CMV Multi-Joint) in subjects.

Secondary

MeasureTime frameDescription
Intra-class correlation coefficient of the inversion force of the foot between two measurements made by the same observer with the hand dynamometer (intra-observer reproducibility).on the day of first evaluation (At day 1) and on the day of second evaluation (at day 2)the inversion force (or supination measured in Newton). The two measurements will be performed during two consultations one day apart.
Intra-class correlation coefficient of the inversion force of the foot between measurements made by two different observers with the hand dynamometer (intra-observer reproducibility).on the day of first evaluation (At day 1) and on the day of second evaluation (at day 2)the inversion force (or supination measured in Newton)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026