Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

Horizontal Plyometric Training and Sprint Mechanics in Early-Adolescent Track-and-Field Athletes (HPT-Sprint You)

30 aprile 2026 aggiornato da: Édison Andrés Pérez Bedoya, Federal University of Vicosa

Effects of Twelve Sessions of Horizontally Oriented Plyometric Training on Sprint-Related Temporal-Kinematic Outcomes in Early-Adolescent Track-and-Field Athletes: A Field-Based Exploratory Pre-Post Study

This field-based exploratory pre-post study examined the effects of a six-week horizontally oriented plyometric training program on sprint performance and sprint-related temporal-kinematic outcomes in early-adolescent male track-and-field athletes. Participants completed 12 supervised plyometric training sessions integrated into their regular athletics practice. Outcomes were assessed at baseline and after the intervention using field-based sprint testing, video-derived temporal-kinematic analysis, and horizontal jump performance measures.

The study was conducted in a low-resource community sport setting in Antioquia, Colombia. The intervention was designed according to the participants' age, training background, and usual sport practice demands, with progressive exercise exposure, supervision, adequate recovery, and safety monitoring throughout the training period.

Panoramica dello studio

Descrizione dettagliata

Horizontally oriented plyometric training may be relevant for sprint development because sprint acceleration and the transition toward maximal sprinting velocity require rapid force production and effective forward orientation of propulsive actions. However, evidence in early-adolescent track-and-field athletes remains limited, particularly in community-based sport contexts where coaches rely on accessible field tests and video-based kinematic procedures.

This exploratory single-arm intervention study evaluated pre-post changes after 12 sessions of horizontally oriented plyometric training in male early-adolescent track-and-field athletes aged 12-13 years. The training program was delivered over approximately six weeks and was integrated into the athletes' regular training routine. The intervention emphasized horizontally directed plyometric actions and was implemented with progressive exposure, technical supervision, adequate rest periods, and suspension criteria in case of pain, excessive fatigue, musculoskeletal discomfort, or any safety concern.

Sprint performance and sprint-related temporal-kinematic variables were assessed before and after the intervention. Field-based assessments included sprint time and video-derived sprint variables, complemented by horizontal jump performance. Because the study was conducted with minors and a small sport-specific sample, all data will be reported in aggregate form, and no individual participant data will be publicly shared.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

9

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

    • Antioquia
      • Guarne, Antioquia, Colombia, 054080
        • Tecnológico de Antioquia

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

Accetta volontari sani

Descrizione

Inclusion Criteria:

  • Male early-adolescent track-and-field athletes aged 12-13 years.
  • Active participation in a municipal or community-based athletics training program in Antioquia, Colombia.
  • Minimum recent experience in athletics training according to the records of the local training program.
  • Ability to complete sprint testing, jump testing, and the planned plyometric training sessions.
  • Written informed consent provided by a parent or legal guardian.
  • Written or documented assent provided by the minor participant.

Exclusion Criteria:

  • Current musculoskeletal injury, pain, or medical restriction that prevents sprinting, jumping, or participation in plyometric training.
  • Any cardiovascular, neurological, orthopedic, or other health condition contraindicating high-intensity physical exercise.
  • Failure to complete baseline or post-intervention assessments.
  • Absence from a substantial portion of the intervention sessions, according to the predefined adherence criteria.
  • Participation in another structured training or research intervention that could substantially affect the outcomes during the study period.

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: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Horizontal Plyometric Training
Participants completed a six-week horizontally oriented plyometric training program consisting of 12 supervised sessions integrated into their regular athletics training. The program emphasized horizontally directed jumping and bounding actions relevant to sprint acceleration and forward propulsion. Training exposure was adjusted according to participants' age, experience, and tolerance, with progressive loading, technical supervision, adequate rest intervals, and safety monitoring.
The intervention consisted of 12 supervised sessions of horizontally oriented plyometric exercises delivered over approximately six weeks. Exercises emphasized forward-directed explosive actions and horizontal force application through age-appropriate plyometric tasks. Sessions were conducted under supervision and incorporated warm-up, technical instruction, controlled progression of volume and intensity, rest periods, and monitoring for pain, excessive fatigue, or musculoskeletal discomfort.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in 60-m Sprint Time
Lasso di tempo: Baseline and within 48-72 hours after the final intervention session.
Total time to complete a 60-m sprint, measured in seconds under field-based conditions. Lower values indicate better sprint performance.
Baseline and within 48-72 hours after the final intervention session.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in Sprint Split Times
Lasso di tempo: Baseline and within 48-72 hours after the final intervention session.
Sprint segment times derived from field-based sprint testing. Segment times will be used to describe changes in sprint acceleration and sprint performance distribution across the sprint distance. Lower values indicate better segment performance.
Baseline and within 48-72 hours after the final intervention session.
Change in Video-Derived Sprint Temporal-Kinematic Variables
Lasso di tempo: Baseline and within 48-72 hours after the final intervention session.
Sprint-related temporal-kinematic variables derived from video analysis during sprint testing. These variables may include step-related temporal and spatial indicators according to the available video-based analysis protocol.
Baseline and within 48-72 hours after the final intervention session.
Change in Horizontal Jump Performance
Lasso di tempo: Baseline and within 48-72 hours after the final intervention session.
Horizontal jump performance assessed using a field-based jump test. Greater jump distance indicates better horizontal explosive performance.
Baseline and within 48-72 hours after the final intervention session.
Adverse Events During Training
Lasso di tempo: From the first intervention session to the final intervention session, approximately six weeks.
Any pain, musculoskeletal discomfort, excessive fatigue, or event requiring interruption, modification, or suspension of the training session will be recorded throughout the intervention.
From the first intervention session to the final intervention session, approximately six weeks.

Collaboratori e investigatori

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

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Pubblicazioni generali

  • McKay AKA, Stellingwerff T, Smith ES, Martin DT, Mujika I, Goosey-Tolfrey VL, Sheppard J, Burke LM. Defining training and performance caliber: A participant classification framework. International Journal of Sports Physiology and Performance. 2022;17(2):317-331.
  • Rumpf MC, Lockie RG, Cronin JB, Jalilvand F. Effect of different sprint training methods on sprint performance over various distances: A brief review. Journal of Strength and Conditioning Research. 2016;30(6):1767-1785.
  • Ramírez-Campillo R, Meylan C, Álvarez C, Henríquez-Olguín C, Martínez C, Cañas-Jamett R, Andrade DC, Izquierdo M. Effects of in-season low-volume high-intensity plyometric training on explosive actions and endurance of young soccer players. Journal of Strength and Conditioning Research. 2014;28(5):1335-1342.
  • Moran J, Sandercock GRH, Ramírez-Campillo R, Wooller JJ, Logothetis S, Schoenmakers PPJM, Parry DA. Maturation-related adaptations in running speed in response to sprint training in youth soccer players. Journal of Strength and Conditioning Research. 2017;31(2):347-352.
  • Lloyd RS, Oliver JL. The youth physical development model: A new approach to long-term athletic development. Strength and Conditioning Journal. 2012;34(3):61-72.

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)

1 luglio 2022

Completamento primario (Effettivo)

1 luglio 2022

Completamento dello studio (Effettivo)

30 agosto 2022

Date di iscrizione allo studio

Primo inviato

30 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

30 aprile 2026

Primo Inserito (Effettivo)

6 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

6 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

30 aprile 2026

Ultimo verificato

1 aprile 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • TdeA-HPT-Sprint-Youth-2026

Piano per i dati dei singoli partecipanti (IPD)

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

NO

Descrizione del piano IPD

Individual participant data will not be shared because the study involved minors and a small sport-specific sample, which may increase the risk of indirect identification. Results will be reported only in aggregate form. De-identified summary data may be made available upon reasonable request when compatible with the ethics approval, participant consent, and institutional data protection requirements.

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 .

Sottoscrivi