- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07665138
Sequence-Dependent Performance Adaptations Following Myofascial Chain Training in Youth Football Players
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.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
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.
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
Mersin
-
Mersin, Mersin, Türkei (türkiye), 33343
- Mersin University
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Kind
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Beschreibung
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
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Sonstiges
- Zuteilung: Zufällig
- Interventionsmodell: Crossover-Aufgabe
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: 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.
|
|
Experimental: 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.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Countermovement Jump (CMJ) Height
Zeitfenster: 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)
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Dynamic Balance - YBT
Zeitfenster: 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)
|
Mitarbeiter und Ermittler
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Andere Studien-ID-Nummern
- MEU-SBF-IK-01
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Beschreibung des IPD-Plans
IPD-Sharing-Zeitrahmen
IPD-Sharing-Zugriffskriterien
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
Klinische Studien zur Posterior chain myofascial training
-
Dow University of Health SciencesAbgeschlossenSchmerzen im unteren RückenPakistan
-
Universidad de AlmeriaNoch keine Rekrutierung
-
Kanuni Sultan Suleyman Training and Research HospitalNoch keine RekrutierungDranginkontinenzTürkei (türkiye)