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Effects of Whole-Body Vibration on Heart Rate Variability During Post-Exercise Recovery (WBV-HRV)

6 de noviembre de 2026 actualizado por: Hamza Budak

Effects of Whole-Body Vibration Versus Passive Recovery on Frequency-Domain Heart Rate Variability Following High-Intensity Exercise: A Randomized Crossover Trial

This study aims to investigate the acute effects of whole-body vibration (WBV) and passive recovery on heart rate variability (HRV) following high-intensity intermittent exercise in male soccer players.

Ten male soccer players will participate in a randomized, two-period crossover study. Each participant will complete two experimental sessions separated by a seven-day washout period. During each session, participants will perform the Yo-Yo Intermittent Recovery Test Level 1 until exhaustion, followed by either 15 minutes of seated whole-body vibration or 15 minutes of seated passive recovery.

During the WBV condition, participants will remain seated with their knees flexed at approximately 90 degrees and their bare feet positioned on a vibration platform operating at 35 Hz with a peak-to-peak amplitude of 2 mm. During passive recovery, participants will remain seated without vibration.

Heart rate variability will be continuously recorded throughout the exercise test and the entire 15-minute recovery period using a chest-strap heart rate sensor. Frequency-domain HRV parameters, including very-low-frequency (VLF), low-frequency (LF), and high-frequency (HF) power, will be analyzed.

The study will compare the autonomic responses associated with the two recovery methods to determine whether seated whole-body vibration produces different short-term HRV responses compared with passive recovery.

Descripción general del estudio

Descripción detallada

This study is designed as a randomized, two-period crossover trial to examine the acute effects of whole-body vibration (WBV) and passive recovery on frequency-domain heart rate variability (HRV) following exhaustive intermittent exercise.

Ten male soccer players will participate in the study. Participants will be randomly assigned to one of two intervention sequences: WBV followed by passive recovery (AB) or passive recovery followed by WBV (BA). A seven-day washout period will separate the experimental sessions to minimize potential carryover effects.

At each experimental session, participants will complete the Yo-Yo Intermittent Recovery Test Level 1 until voluntary exhaustion. Following exercise, participants will undergo a 15-minute recovery intervention according to their assigned sequence.

During the WBV intervention, participants will sit on a chair with their knees flexed at approximately 90 degrees and their bare feet placed on a vertical vibration platform operating at 35 Hz with a peak-to-peak displacement of 2 mm. During the passive recovery intervention, participants will remain seated in a comparable position with their feet resting on the floor and without vibration exposure.

Heart rate variability will be recorded continuously throughout the exercise test and the complete 15-minute recovery period using a Polar H10 chest-strap sensor. HRV data will be processed using Kubios HRV software to obtain frequency-domain parameters, including VLF, LF, and HF power.

The primary objective is to compare frequency-domain HRV responses between WBV and passive recovery conditions. Statistical analyses will account for the paired crossover design and evaluate differences between recovery conditions.

The findings are expected to contribute to the understanding of acute autonomic responses to whole-body vibration as a post-exercise recovery intervention in soccer players.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

10

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.

Estudio Contacto

Ubicaciones de estudio

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 40 años (Adulto)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Masculino

Descripción

Inclusion Criteria:

  • Male soccer players within the predefined eligible age range.
  • Regular participation in soccer training.
  • Ability to complete the Yo-Yo Intermittent Recovery Test Level 1.
  • Willingness to participate in both experimental sessions.
  • Provision of written informed consent.

Exclusion Criteria:

  • Known cardiovascular, neurological, or musculoskeletal disorders that could affect exercise performance or heart rate variability.
  • Current injury or illness preventing maximal exercise.
  • Use of medications known to influence autonomic nervous system activity or heart rate variability.
  • Any contraindication to whole-body vibration exposure.

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: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación cruzada
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Sequence AB (WBV → Passive Recovery)

Participants assigned to Sequence AB will undergo whole-body vibration (WBV) recovery during the first experimental period, followed by passive recovery during the second period. A seven-day washout period will separate the two sessions. Both recovery interventions will last 15 minutes and will be performed in a seated position following the Yo-Yo Intermittent Recovery Test Level 1. During WBV recovery, participants will remain seated with their feet placed on the vibration platform, operating at 35 Hz and 2 mm peak-to-peak amplitude.

Participants assigned to the whole-body vibration (WBV) intervention will undergo a 15-minute recovery session immediately following the Yo-Yo Intermittent Recovery Test Level 1. During the intervention, participants will remain seated on a chair with their knees flexed at approximately 90 degrees and their bare feet placed on a vertical vibration platform. The platform will operate at a frequency of 35 Hz and a peak-to-peak amplitude of 2 mm. Heart rate variability will be continuously recorded throughout the 15-minute recovery period to evaluate autonomic nervous system responses.

Participants assigned to the passive recovery intervention will undergo a 15-minute seated recovery session immediately following the Yo-Yo Intermittent Recovery Test Level 1. During this period, participants will remain seated on a chair with their feet resting on the floor, without receiving whole-body vibration or any other active recovery intervention. Heart rate variability will be continuously recorded throughout the 15-minute recovery period to evaluate autonomic nervous system responses.

Experimental: Sequence BA (Passive Recovery → WBV)

Participants assigned to Sequence BA will undergo passive recovery during the first experimental period, followed by whole-body vibration (WBV) recovery during the second period. A seven-day washout period will separate the two sessions. Both recovery interventions will last 15 minutes and will be performed in a seated position following the Yo-Yo Intermittent Recovery Test Level 1. During passive recovery, participants will remain seated with their feet resting on the floor. During WBV recovery, participants will remain seated with their feet placed on the vibration platform, operating at 35 Hz and 2 mm peak-to-peak amplitude.

Participants assigned to the whole-body vibration (WBV) intervention will undergo a 15-minute recovery session immediately following the Yo-Yo Intermittent Recovery Test Level 1. During the intervention, participants will remain seated on a chair with their knees flexed at approximately 90 degrees and their bare feet placed on a vertical vibration platform. The platform will operate at a frequency of 35 Hz and a peak-to-peak amplitude of 2 mm. Heart rate variability will be continuously recorded throughout the 15-minute recovery period to evaluate autonomic nervous system responses.

Participants assigned to the passive recovery intervention will undergo a 15-minute seated recovery session immediately following the Yo-Yo Intermittent Recovery Test Level 1. During this period, participants will remain seated on a chair with their feet resting on the floor, without receiving whole-body vibration or any other active recovery intervention. Heart rate variability will be continuously recorded throughout the 15-minute recovery period to evaluate autonomic nervous system responses.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Very Low Frequency (VLF) Power
Periodo de tiempo: During the exercise test and the subsequent 15-minute recovery period in each experimental session.

Very low frequency (VLF) power is a frequency-domain parameter of heart rate variability (HRV), expressed in ms². HRV will be continuously recorded using a Polar H10 chest strap during the entire exercise test and the 15-minute recovery period. VLF power will be analyzed using Kubios HRV software to assess autonomic responses under whole-body vibration and passive recovery conditions.

During the exercise test and the subsequent 15-minute recovery period in each experimental session.
Low Frequency (LF) Power
Periodo de tiempo: During the exercise test and the subsequent 15-minute recovery period in each experimental session.

Low frequency (LF) power is a frequency-domain parameter of heart rate variability (HRV), expressed in ms². HRV will be continuously recorded using a Polar H10 chest strap during the entire exercise test and the 15-minute recovery period. LF power will be analyzed using Kubios HRV software to evaluate autonomic responses under whole-body vibration and passive recovery conditions.

During the exercise test and the subsequent 15-minute recovery period in each experimental session.
High Frequency (HF) Power
Periodo de tiempo: During the exercise test and the subsequent 15-minute recovery period in each experimental session.

High frequency (HF) power is a frequency-domain parameter of heart rate variability (HRV), expressed in ms², and is commonly used as an indicator of cardiac parasympathetic modulation. HRV will be continuously recorded using a Polar H10 chest strap during the entire exercise test and the 15-minute recovery period. HF power will be analyzed using Kubios HRV software to compare responses between whole-body vibration and passive recovery conditions.

During the exercise test and the subsequent 15-minute recovery period in each experimental session.

Colaboradores e Investigadores

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

Patrocinador

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 (Estimado)

17 de noviembre de 2026

Finalización primaria (Estimado)

24 de noviembre de 2026

Finalización del estudio (Estimado)

24 de noviembre de 2026

Fechas de registro del estudio

Enviado por primera vez

6 de noviembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

6 de noviembre de 2026

Publicado por primera vez (Actual)

12 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

12 de noviembre de 2026

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

6 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 and data protection considerations. Only aggregated and anonymized study results will be reported in scientific publications.

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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