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

30 de abril de 2026 actualizado por: 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.

Descripción general del estudio

Descripción detallada

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 de estudio

Intervencionista

Inscripción (Actual)

9

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

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

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Niño

Acepta Voluntarios Saludables

Sí

Descripción

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.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Otro
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in 60-m Sprint Time
Periodo de tiempo: 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.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in Sprint Split Times
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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.

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

  • 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.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

1 de julio de 2022

Finalización primaria (Actual)

1 de julio de 2022

Finalización del estudio (Actual)

30 de agosto de 2022

Fechas de registro del estudio

Enviado por primera vez

30 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

30 de abril de 2026

Publicado por primera vez (Actual)

6 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

6 de mayo de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

30 de abril de 2026

Última verificación

1 de abril de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • TdeA-HPT-Sprint-Youth-2026

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan 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.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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