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Effects of Different High-Intensity Interval Training Protocols on Physiological and Skeletal Muscle Adaptations in Healthy Young Men

4 de noviembre de 2026 actualizado por: Gdansk University of Physical Education and Sport

This study investigated the effects of different high-intensity interval training protocols on physical fitness and physiological adaptations in healthy young men.

Participants underwent a two-week exercise training program consisting of six sessions performed three times per week. Four training protocols were investigated, differing in exercise intensity, duration of exercise bouts, and recovery periods.

The primary outcome was the change in maximal oxygen uptake (VO2max), an indicator of aerobic fitness. Additional assessments included cognitive performance, measured using tests of attention, processing speed, and inhibitory control, as well as selected physiological and skeletal muscle adaptations.

The study aimed to improve understanding of how different high-intensity interval training protocols influence aerobic fitness and other physiological responses over a short training period.

Descripción general del estudio

Descripción detallada

High-intensity interval training (HIIT) and sprint interval training (SIT) are exercise strategies characterized by repeated bouts of vigorous or maximal exercise interspersed with recovery periods. These training approaches may induce physiological adaptations within relatively short intervention periods. However, the effects of different combinations of exercise duration, intensity, and recovery time on aerobic fitness, cognitive performance, and skeletal muscle adaptations require further investigation.

This interventional study examined physiological responses to four cycling-based high-intensity training protocols in healthy young men. Participants completed six training sessions over two weeks, with three sessions performed each week.

The investigated protocols included:

SIT10:1: Repeated 10-second maximal cycling sprints separated by 60-second recovery periods.

SIT10:4: Repeated 10-second maximal cycling sprints separated by 240-second recovery periods.

HIIT90:180: Six 90-second cycling intervals performed at 80% of maximal aerobic power, separated by 180-second passive recovery periods.

Wingate-SIT: Repeated 30-second all-out cycling sprints using a Wingate-based protocol.

The primary outcome was the change in maximal oxygen uptake (VO2max), assessed using incremental exercise testing before and after the intervention. Additional assessments included cognitive performance using the Stroop Color-Word Test, Trail Making Test, and Digit Span Test, as well as selected measures of exercise performance and skeletal muscle metabolic adaptations.

Skeletal muscle biopsies were collected from subsets of participants before and after training to investigate exercise-induced adaptations in muscle tissue. Stored biopsy samples were subsequently used for exploratory proteomic analyses.

The study was designed to characterize short-term physiological and skeletal muscle responses to different high-intensity interval exercise protocols.

Tipo de estudio

Intervencionista

Inscripción (Actual)

50

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

    • Pomeranian
      • Gdansk, Pomeranian, Polonia, 80-336
        • Gdansk University of Physical Education and Sport

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

18 años a 35 años (Adulto)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Masculino

Descripción

Inclusion Criteria:

Healthy adult males. Physically active individuals. Ability to perform high-intensity cycling exercise. Willingness to participate in the two-week training intervention and complete the required assessments.

Provision of written informed consent.

Exclusion Criteria:

Known cardiovascular, respiratory, metabolic, or neurological disorders that could affect exercise performance or participant safety.

Musculoskeletal injuries or conditions preventing participation in high-intensity cycling exercise.

Medical contraindications to maximal exercise testing or sprint interval training.

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: Ciencia básica
  • Asignación: No aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: SIT10:1 - Short-Recovery Sprint Interval Training

Participants completed a two-week cycling sprint interval training program comprising six sessions (three sessions per week). The protocol involved repeated 10-second maximal cycling sprints separated by 60-second recovery intervals.

A two-week cycling sprint interval training intervention consisting of six sessions performed three times per week. Participants performed repeated 10-second maximal cycling sprints interspersed with 60-second recovery intervals.

Experimental: SIT10:4 - Long-Recovery Sprint Interval Training

Participants completed a two-week cycling sprint interval training program comprising six sessions (three sessions per week). The protocol involved repeated 10-second maximal cycling sprints separated by 240-second recovery intervals.

A two-week cycling sprint interval training intervention consisting of six sessions performed three times per week. Participants performed repeated 10-second maximal cycling sprints interspersed with 240-second recovery intervals.

Experimental: HIIT90:180 - High-Intensity Interval Training

Participants completed a two-week high-intensity interval cycling program consisting of six supervised training sessions (three sessions per week). Each session included six 90-second cycling bouts performed at 80% of maximal aerobic power, separated by 180-second passive recovery intervals. Exercise cadence was maintained at approximately 60 revolutions per minute.

A two-week cycling high-intensity interval training intervention comprising six supervised sessions performed three times per week. Each session consisted of six 90-second exercise bouts at 80% of maximal aerobic power, separated by 180-second passive recovery intervals. Cycling cadence was approximately 60 revolutions per minute.

Experimental: Wingate-SIT - Wingate-Based Sprint Interval Training

Participants completed a two-week sprint interval training program comprising six cycling sessions (three sessions per week). The intervention consisted of repeated 30-second all-out cycling sprints performed using a Wingate-based protocol, with recovery periods between successive efforts.

A two-week cycling sprint interval training intervention comprising six sessions performed three times per week. Participants performed repeated 30-second all-out cycling sprints using a Wingate-based protocol, with recovery intervals between successive sprints.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in Maximal Oxygen Uptake (VO2max)
Periodo de tiempo: Baseline and after the 2-week training intervention

Change in maximal oxygen uptake (VO2max), expressed in mL/kg/min, assessed using an incremental exercise test before and after the two-week training intervention.

Baseline and after the 2-week training intervention

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in Cognitive Performance
Periodo de tiempo: Baseline and after the 2-week training intervention

Changes in cognitive performance assessed using the Stroop Color-Word Test (inhibitory control), Trail Making Test (processing speed and executive function), and Digit Span Test (working memory), before and after the two-week training intervention.

Baseline and after the 2-week training intervention
Change in Skeletal Muscle Oxidative Enzyme Activity
Periodo de tiempo: Baseline and after the 2-week training intervention

Changes in skeletal muscle oxidative enzyme activity assessed in biopsy samples collected before and after the two-week training intervention. Muscle biopsies were performed in a subset of participants who provided additional informed consent for the procedure.

Baseline and after the 2-week training intervention

Colaboradores e Investigadores

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

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)

10 de febrero de 2013

Finalización primaria (Actual)

17 de abril de 2018

Finalización del estudio (Actual)

30 de diciembre de 2018

Fechas de registro del estudio

Enviado por primera vez

4 de noviembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

4 de noviembre de 2026

Publicado por primera vez (Actual)

9 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

9 de noviembre de 2026

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

4 de noviembre de 2026

Última verificación

1 de noviembre de 2026

Más información

Términos relacionados con este estudio

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 made publicly available due to participant confidentiality considerations and the absence of a data-sharing plan in the original study protocol.

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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