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Sequence-Dependent Performance Adaptations Following Myofascial Chain Training in Youth Football Players

24 juin 2026 mis à jour par: Inci Kesilmis, Mersin University

Sequence-Dependent Performance Adaptations Following Myofascial Chain Training in Youth Football Players: An Integrated Statistical and Knowledge Graph Approach

This study looked at whether the order of two different types of muscle-and-connective-tissue ("myofascial chain") training affects how young football players improve their jumping power and balance.

Forty male football players, aged 15 to 16, took part. Players were split into two groups by chance. One group did "posterior chain" training first, then switched to "spiral chain" training. The other group did the trainings in the opposite order. Each training phase lasted six weeks, and players kept doing their normal team practice at the same time.

Jumping power and balance were measured four times: before training started, after the first six weeks, after the second six weeks, and again four weeks after training ended.

The goal was to find out if starting with one type of training instead of the other leads to bigger, faster, or longer-lasting improvements. This information may help coaches design better training programs for young athletes.

Aperçu de l'étude

Description détaillée

Myofascial chains are interconnected lines of muscle and connective tissue that transmit force across body segments, contributing to movement efficiency, joint stability, and elastic energy storage. Among the chains described in fascial anatomy literature, the posterior chain is considered a primary contributor to explosive force production, while the spiral chain contributes to rotational control and dynamic balance. Despite growing interest in fascia-informed training approaches, no prior study has examined whether the sequence in which these chains are trained influences the magnitude, time-course, or persistence of performance adaptations in youth athletes.

To address this gap, the study employed a randomized crossover design. Participants were randomly allocated in a 1:1 ratio to one of two sequence groups: the Posterior Chain First Group (PCFG) or the Spiral Chain First Group (SCFG). Both groups continued their regular club training throughout the entire study period.

The intervention consisted of two consecutive six-week training blocks separated by a mid-test assessment. In the first block, each group performed their assigned myofascial chain protocol; following the crossover, groups switched protocols for the second block. Each training session lasted 30 minutes and was completed in addition to routine club practice. Outcomes were assessed at four time points - baseline, after the first block, after the second block, and at a four-week follow-up - to capture both the progression and persistence of adaptations.

The primary aim was to determine whether initiating training with the posterior chain versus the spiral chain produces differential adaptation trajectories, which may inform evidence-based sequencing decisions in youth athlete development programs.

Type d'étude

Interventionnel

Inscription (Réel)

40

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Enfant
  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Oui

La description

IInclusion Criteria:

  • Male, aged 15-16 years (U15-U16 category)
  • Holding an active football player license and currently competing with a club team
  • Regularly participating in routine club training sessions
  • Free from any injury or musculoskeletal condition that could affect performance testing at the time of enrollment
  • Parental/legal guardian consent and participant assent obtained

Exclusion Criteria:

  • Presence of any musculoskeletal injury, recent surgery, or medical condition affecting lower-limb function within the past 6 months
  • Inability to attend the required training sessions or assessment time points
  • Unwillingness or inability of parents/legal guardians to provide informed consent

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Autre
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation croisée
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: PCFG (Posterior Chain First)
Participants performed a posterior chain-focused myofascial training protocol during the first 6-week period, followed by a spiral chain-focused protocol during the second 6-week period, in addition to routine club training.
A 6-week, twice-weekly structured training protocol targeting the posterior myofascial chain, consisting of a warm-up, five functional exercises, and a cool-down phase, delivered in addition to routine club training.
A 6-week, twice-weekly structured training protocol targeting the spiral myofascial chain, consisting of a warm-up, five functional exercises, and a cool-down phase, delivered in addition to routine club training.
Expérimental: SCFG (Spiral Chain First)
Participants performed a spiral chain-focused myofascial training protocol during the first 6-week period, followed by a posterior chain-focused protocol during the second 6-week period, in addition to routine club training.
A 6-week, twice-weekly structured training protocol targeting the posterior myofascial chain, consisting of a warm-up, five functional exercises, and a cool-down phase, delivered in addition to routine club training.
A 6-week, twice-weekly structured training protocol targeting the spiral myofascial chain, consisting of a warm-up, five functional exercises, and a cool-down phase, delivered in addition to routine club training.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Countermovement Jump (CMJ) Height
Délai: Measured at baseline (pre-test), 6 weeks (mid-test), 12 weeks (post-test), and 4 weeks post-test (follow-up)
Lower-limb explosive power was assessed using the countermovement jump, measured with a photocell device (SE-JP1). Each participant performed three non-consecutive jumps with hands on hips, and the mean of the three trials was used for analysis.
Measured at baseline (pre-test), 6 weeks (mid-test), 12 weeks (post-test), and 4 weeks post-test (follow-up)

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Dynamic Balance - YBT
Délai: Measured at baseline (pre-test), 6 weeks (mid-test), 12 weeks (post-test), and 4 weeks post-test (follow-up)
Dynamic balance was assessed using the Y-Balance Test with the right/left leg as the stance leg, measuring reach distance (cm) in the anterior, posteromedial, and posterolateral directions, normalized to leg length.
Measured at baseline (pre-test), 6 weeks (mid-test), 12 weeks (post-test), and 4 weeks post-test (follow-up)

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

5 mai 2025

Achèvement primaire (Réel)

1 septembre 2025

Achèvement de l'étude (Réel)

22 décembre 2025

Dates d'inscription aux études

Première soumission

18 juin 2026

Première soumission répondant aux critères de contrôle qualité

18 juin 2026

Première publication (Réel)

24 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

29 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

24 juin 2026

Dernière vérification

1 juin 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • MEU-SBF-IK-01

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

OUI

Description du régime IPD

De-identified individual participant data underlying the results reported in this article (CMJ and Y-Balance Test scores at all four assessment time points), along with the study protocol.

Délai de partage IPD

Beginning 3 months and ending 5 years after article publication

Critères d'accès au partage IPD

Investigators who provide a methodologically sound proposal, for use in achieving the aims of the approved proposal. Requests should be directed to the corresponding author.

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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