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

24 giugno 2026 aggiornato da: 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.

Panoramica dello studio

Descrizione dettagliata

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.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

40

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino
  • Adulto
  • Adulto più anziano

Accetta volontari sani

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Altro
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione incrociata
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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.
Sperimentale: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Countermovement Jump (CMJ) Height
Lasso di tempo: 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)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Dynamic Balance - YBT
Lasso di tempo: 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)

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

5 maggio 2025

Completamento primario (Effettivo)

1 settembre 2025

Completamento dello studio (Effettivo)

22 dicembre 2025

Date di iscrizione allo studio

Primo inviato

18 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

18 giugno 2026

Primo Inserito (Effettivo)

24 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

29 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

24 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • MEU-SBF-IK-01

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

Descrizione del piano 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.

Periodo di condivisione IPD

Beginning 3 months and ending 5 years after article publication

Criteri di accesso alla condivisione 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.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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