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Clinical Trials/NCT05574322
NCT05574322
Recruiting
Not Applicable

Efficacy of a Foot Strengthening Protocol on Sport Performance Kinetics

Centre Hospitalier Universitaire de Saint Etienne1 site in 1 country72 target enrollmentFebruary 3, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy Athletes
Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Enrollment
72
Locations
1
Primary Endpoint
maximal isometric joint flexion muscle strength MTP (in N)
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

This randomized controlled trial aims to explore the effect of a foot strengthening protocol on toe flexion strength, foot deformation and morphology as well as kinetics during sprinting, cutting and jumping in healthy athletes (18-40 completed years). The study consists of a 4 weeks control period, followed by 8 weeks intervention period and 4 weeks follow up

Detailed Description

During the first period participants are unaware of their allocation, while in the intervention period they will be allocated to a train intervention or a control group (habits maintenance). The primary outcome is the toes maximal voluntary isometric plantarflexion. The treatment effectiveness estimand is the same as in a pretest-posttest case control study, considering the end of the control period as pre-point. An estimation of the individual variability in response to the treatment will be provided.

Registry
clinicaltrials.gov
Start Date
February 3, 2023
End Date
May 2026
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

maximal isometric joint flexion muscle strength MTP (in N)

Time Frame: Change from baseline to Week 18

It will be measured using an ergometer composed of a 3-dimensional force sensor (Nano 25, ATI Industrial Automation, Garner, NC) during the 3 periods of the randomized controlled trial (control, intervention and follow-up) and repeatedly each week during the intervention protocol.

Secondary Outcomes

  • Foot posture(Change from baseline to Week 18)
  • propulsion impulse during jumps(Change from baseline to Week 18)
  • Morphology of the foot muscles(Change from baseline to Week 18)
  • general stiffness of the foot-ankle complex(Change from baseline to Week 18)
  • propulsion impulse during direction changes(Change from baseline to Week 18)
  • Foot deformity(Change from baseline to Week 18)
  • propulsion impulse during sprinting(Change from baseline to Week 18)

Study Sites (1)

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