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Comparison of Training Intensity Distribution Models in Recreational Distance Runners

6 de mayo de 2026 actualizado por: Luis Eduardo Ranieri, Universidad Rey Juan Carlos

Comparison of Polarized, Pyramidal, and Threshold Training Intensity Distribution on Physiological and Performance Outcomes in Recreational Distance Runners

This study aims to compare the effects of three different training intensity distribution (TID) models-polarized, threshold, and pyramidal-on physiological and performance adaptations in recreational distance runners. Twenty-four participants will be assigned to one of the three training interventions and will complete an 8-week structured running program based on the respective TID approach.

The primary objective is to determine whether different TID models elicit distinct changes in key physiological markers and endurance performance. The study seeks to answer whether a specific intensity distribution strategy provides superior adaptations in recreational runners when training is prescribed over a controlled intervention period.

Descripción general del estudio

Descripción detallada

This study adopts a parallel-group experimental design to compare the effects of three training intensity distribution (TID) models-polarized, threshold, and pyramidal-on physiological and performance adaptations in recreational distance runners.

Eligible participants are required to be recreational runners with a minimum training frequency of four sessions per week. Following enrollment, all participants complete a one-week pre-intervention phase dedicated to baseline assessments and familiarization with testing procedures.

During this phase, participants will performe a comprehensive physiological evaluation to determine key endurance-related variables. These include ventilatory thresholds (e.g., VT1 and VT2), running economy, and maximal oxygen uptake (VO₂max), assessed through an incremental exercise test under standardized laboratory conditions. In addition, participants perform a 5-km time trial on a standardized course or controlled conditions to assess endurance performance.

Based on the physiological assessment, individual training intensities are prescribed using a five-zone intensity model derived from ventilatory thresholds and maximal aerobic capacity. This approach allows for precise classification of training load and ensures consistency in the application of the three TID models across participants.

Following baseline testing, participants are allocated to one of the three intervention groups (polarized, threshold, or pyramidal) and complete an 8-week structured endurance training program. Each training model differs in the relative distribution of time spent across the five intensity zones, while overall training frequency and general structure are maintained comparable between groups.

Training sessions are monitored using participants' GPS-enabled sport watches, which record variables such as duration, distance, pace, and heart rate. These data are used to quantify training load and verify adherence to the prescribed intensity distribution. Participants are instructed to follow the assigned training program and upload their training data regularly for supervision and compliance tracking.

At the end of the 8-week intervention, all baseline assessments are repeated under the same conditions. This includes the physiological testing to reassess ventilatory thresholds, running economy, and VO₂max, as well as the 5-km time trial to evaluate changes in endurance performance.

The primary aim of the study is to examine whether different TID models induce distinct adaptations in physiological determinants and performance outcomes when applied in a controlled, prospective training intervention in recreational runners.

Tipo de estudio

Intervencionista

Inscripción (Actual)

24

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

    • Madrid
      • Fuenlabrada, Madrid, España, 28943
        • Cam. del Molino, 5, Fuenlabrada, Madrid

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

  • Adulto

Acepta Voluntarios Saludables

Sí

Descripción

Inclusion Criteria:

  • age ≥ 18 years;
  • a habitual training frequency of ≥ 4 sessions·week
  • running experience ≥ 2 years;
  • absence of musculoskeletal injuries in the preceding 3 months

Exclusion Criteria:

  • an official 10-km race time > 40:00 min:s for men and > 50:00 min:s for women
  • any cardiometabolic disease

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: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Polarized training Intensity Distribution
Participants assigned to the polarized training group perform an 8-week structured endurance training program characterized by a high proportion of low-intensity exercise and a smaller proportion of high-intensity exercise, with minimal time spent at moderate intensities. Training intensity is prescribed using an individualized five-zone model based on baseline physiological assessments. The majority of training is performed in the lowest intensity zones (Zones 1-2), while high-intensity sessions are conducted in the highest zones (Zones 4-5). Training load and adherence are monitored using GPS-enabled sport watches.
This intervention consists of an endurance training program based on a polarized intensity distribution model. Training intensity is prescribed using an individualized five-zone system derived from physiological assessments (e.g., ventilatory thresholds and maximal oxygen uptake). The model is characterized by a high proportion of training performed at low intensities (Zones 1-2) and a smaller but meaningful proportion at high intensities (Zones 4-5), with minimal time accumulated at moderate intensities (Zone 3). This distribution aims to maximize adaptations by combining extensive low-intensity volume with targeted high-intensity stimuli.
Otros nombres:
  • POL
Experimental: Threshold Training Intensity Distribution
Participants assigned to the threshold training group complete an 8-week structured endurance training program emphasizing a greater proportion of training at moderate-to-high intensities, particularly around the second ventilatory threshold. Training intensity is prescribed using an individualized five-zone model derived from baseline physiological assessments. A substantial portion of training is performed in intermediate zones (Zones 3-4), with comparatively less time spent at low (Zones 1-2) and high intensities (Zone 5). Training sessions are monitored via GPS-enabled sport watches to ensure adherence.
Participants assigned to the threshold training group complete an 8-week structured endurance training program emphasizing a greater proportion of training at moderate-to-high intensities, particularly around the second ventilatory threshold. Training intensity is prescribed using an individualized five-zone model derived from baseline physiological assessments. A substantial portion of training is performed in intermediate zones (Zones 3-4), with comparatively less time spent at low (Zones 1-2) and high intensities (Zone 5). Training sessions are monitored via GPS-enabled sport watches to ensure adherence.
Otros nombres:
  • THR
Experimental: Pyramidal training Intensity Distribution
Participants assigned to the pyramidal training group perform an 8-week structured endurance training program characterized by a progressive decrease in training volume from low to high intensities. Training intensity is prescribed using an individualized five-zone model based on baseline physiological assessments. Most training is accumulated in low-intensity zones (Zones 1-2), with moderate amounts in intermediate zones (Zone 3) and smaller proportions at higher intensities (Zones 4-5), forming a pyramidal distribution. Training load and compliance are monitored using GPS-enabled sport watches.
Participants assigned to the pyramidal training group perform an 8-week structured endurance training program characterized by a progressive decrease in training volume from low to high intensities. Training intensity is prescribed using an individualized five-zone model based on baseline physiological assessments. Most training is accumulated in low-intensity zones (Zones 1-2), with moderate amounts in intermediate zones (Zone 3) and smaller proportions at higher intensities (Zones 4-5), forming a pyramidal distribution. Training load and compliance are monitored using GPS-enabled sport watches.
Otros nombres:
  • Pyr

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Maximal Oxygen Uptake (VO₂max)
Periodo de tiempo: Baseline to 8 weeks
Assessment of changes in maximal oxygen uptake (VO₂max) obtained during an incremental exercise test. VO₂max is used as a measure of maximal aerobic capacity and cardiorespiratory fitness.
Baseline to 8 weeks
Ventilatory Thresholds and Associated Running Speeds
Periodo de tiempo: Baseline to 8 weeks
Assessment of changes in the first and second ventilatory thresholds (VT1 and VT2) and their corresponding running speeds, determined during an incremental exercise test. These variables reflect submaximal endurance capacity and physiological determinants of performance and their changes after intervention.
Baseline to 8 weeks
Running Economy
Periodo de tiempo: Baseline to 8 weeks
Assessment of changes in running economy, defined as the oxygen cost of running at a standardized submaximal speed during laboratory testing. This measure reflects the efficiency of movement during endurance exercise.
Baseline to 8 weeks
Changes in 5-km time trial performance
Periodo de tiempo: Baseline to 8 weeks
Assessment of changes in endurance performance measured as completion time in a 5-km time trial conducted under standardized conditions. Pre- to post-intervention differences are used to evaluate the effect of the training interventions on real-world running performance.
Baseline to 8 weeks

Colaboradores e Investigadores

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

Investigadores

  • Director de estudio: Arturo Casado, PhD, Universidad Rey Juan Carlos

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

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 abril de 2024

Finalización primaria (Actual)

30 de julio de 2024

Finalización del estudio (Actual)

20 de abril de 2026

Fechas de registro del estudio

Enviado por primera vez

27 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

27 de abril de 2026

Publicado por primera vez (Actual)

4 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

11 de mayo de 2026

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

6 de mayo de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • IND/22HUM-23661-1
  • IND/22HUM-23661 (Otro número de subvención/financiamiento: Comunidad Autonoma de Madrid)

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

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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