AzTrials
AzTrials

Flatfoot, FlexibleNCT07884162

Plyometric vs. Intrinsic Foot Muscle Training in Pediatric Flatfoot

A study testing Plyometric Training in people with Flatfoot, Flexible, run by Faculty of Medicine, Sousse at 1 site in Tunisia.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The purpose of this study is to investigate how the order of exercises in a training program affects foot mechanics and physical performance in children with flexible flatfoot. Flexible flatfoot is common in children and can affect how weight is distributed on the foot, balance, and athletic abilities. Read more about this study

Who is it for?
Ages 9 to 12 years, men only
Conditions the study is for
Flatfoot, Flexible
What is being tested?
Plyometric Training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
36 participants
Where
1 siteTunisia
Study dates
15 Nov 2025to 15 May 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 9 to 12 years
  • Men only
  • No healthy volunteers
  • Child

Who may be able to join

  • Participants were required to be actively practising youth football players aged between 9 and 12 years with a clinically and podographically confirmed diagnosis of bilateral flexible flatfoot according to the study's predefined diagnostic criteria.

Who cannot join

  • Participants were excluded if they presented any history of lower limb orthopaedic surgery, a musculoskeletal injury within the preceding six months, or a diagnosed neurological disorder.

Trial locations and contacts

1 site in 1 country.

Tunisia1 site
  • Research Laboratory (LR19ES09), Exercise Physiology and Pathophysiology, Faculty of Medicine of Sousse, University of Sousse

    Sousse, 4002

Other trials in Tunisia

About this study

Official title: Plyometric-First Versus Intrinsic Foot Muscle-First Training in Children With Flexible Flatfoot: Effects on Plantar Loading and Athletic Performance

The purpose of this study is to investigate how the order of exercises in a training program affects foot mechanics and physical performance in children with flexible flatfoot. Flexible flatfoot is common in children and can affect how weight is distributed on the foot, balance, and athletic abilities. While both foot-strengthening exercises and jump training (plyometrics) are helpful, it is not known which one should be done first to get the best results.

In this study, thirty-six young male football players with flexible flatfoot were divided into three groups. The first group performed jump training followed by foot muscle strengthening. The second group did the foot muscle strengthening first, followed by jump training. The third group served as a control group and did not change their usual training. The researchers measured changes in foot pressure, balance, jumping height, muscle force, and sprint speed before and after the training to find out which exercise order is most effective for improving athletic performance and foot loading.

Read the detailed description

This study evaluates the impact of exercise sequencing within a combined training program for young athletes with flexible flatfoot. Participants are block-randomized into three distinct parallel arms to compare different training structures over the intervention period:

  • Group P1-R2: Participants undergo plyometric training in the first phase, followed by intrinsic foot muscle (IFM) strengthening in the second phase.
  • Group R1-P2: Participants undergo intrinsic foot muscle (IFM) strengthening in the first phase, followed by plyometric training in the second phase.
  • Control Group (CG): Participants maintain their habitual football training schedule without any additional specific foot or plyometric interventions.

All participants undergo a comprehensive testing battery at baseline (pre-intervention) and immediately following the completion of the training protocol (post-intervention). The assessments include static and dynamic baropodometric analyses to measure peak plantar pressure, postural tracking to evaluate balance, countermovement jump (CMJ) tests for neuromuscular mechanics, eccentric rate of force development (RFD) evaluations, and 20-meter timed sprints to quantify locomotor performance.

Being tested
Plyometric Training
Keywords
Intrinsic foot muscles; Plyometric training; Postural stability; Exercise sequencing; Paediatric biomechanics
Medical subject headings
Flatfoot

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Plyometric TrainingBehavioural

    Jump and plyometric exercises performed 3 times per week for a total duration of 4 weeks. This intervention is implemented during Phase 1 for Group P1-R2 and during Phase 2 for Group R1-P2.

Study groups in NCT07884162
Study groupRoleWhat they receive
Group P1-R2ExperimentalPediatric football players with flexible flatfoot who undergo a combined training program consisting of 4 weeks of plyometric training (Phase 1) followed by 4 weeks of intrinsic foot muscle strengthening (Phase 2), performed 3 times per week for a total of 8 weeks.
Receives: Behavioral: Plyometric Training
Group R1-P2ExperimentalA separate group of pediatric football players with flexible flatfoot who undergo the inverse sequence: 4 weeks of intrinsic foot muscle strengthening (Phase 1) followed by 4 weeks of plyometric training (Phase 2), performed 3 times per week for a total of 8 weeks.
Receives: Behavioral: Plyometric Training
Control GroupNo interventionA third separate group of pediatric football players with flexible flatfoot who maintain their habitual football training schedule without participating in any specific plyometric or foot muscle strengthening protocols during the 8-week study period.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Peak Plantar Pressure

    Static and dynamic peak plantar pressure assessed using baropodometric analysis to evaluate changes in plantar loading.

    Measured: Baseline (before the intervention) and post-intervention (after 8 weeks of training).

Secondary outcomes (1)
  1. Postural Balance Tracking

    Postural stability tracking parameters evaluated under static and dynamic conditions.

    Measured: Baseline (before the intervention) and post-intervention (after 8 weeks of training).

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Oct 2026
  2. Study start15 Nov 2025
  3. Primary completion26 Jan 2026
  4. Study completion15 May 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Single group
Model description
This study utilizes a three-arm parallel group design to investigate the effects of exercise sequencing within a combined training program. Although the experimental groups are named after the order of their training components (plyometric-first vs. intrinsic foot muscle-first), participants remain within their randomly assigned group for the entire 8-week duration. The total intervention is structurally divided into two consecutive 4-week phases for both experimental arms, while the control group concurrently maintains habitual training, ensuring a direct parallel comparison of the two distinct sequences against a control baseline.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
36 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07884162
Sponsor's protocol ID
CEFMSo_0160_2025
Status last verified
Nov 2025
First submitted
13 Oct 2026
Last updated
20 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data will not be shared outside of the research team to maintain participant confidentiality, as explicit consent for public data repository sharing was not obtained from the legal guardians at the time of enrollment.

Questions about this trial

What is this clinical trial studying?

A study testing Plyometric Training in people with Flatfoot, Flexible, run by Faculty of Medicine, Sousse at 1 site in Tunisia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 20 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Tunisia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Peak Plantar Pressure (time frame: Baseline (before the intervention) and post-intervention (after 8 weeks of training).). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Oct 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in