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Does Wearing Compression Garments Affect Sleep in Soccer Players

30 de agosto de 2026 actualizado por: Wael Daab, Universite de Picardie Jules Verne

Does Wearing Compression Garments Affect Sleep in Soccer Players? A Randomized-controlled Cross-over Study From a Professional Soccer Club Academy

This study investigated the effects of nocturnal compression garments on sleep quantity and quality in young elite male soccer players. Eighteen players participated in a randomized controlled crossover protocol conducted over four consecutive weeks. During the first week, participants completed a control condition without wearing compression garments. During the following three weeks, they completed three experimental conditions in randomized order: full compression leggings, compression calf sleeves, and non-compressive placebo garments. Each condition was performed for seven consecutive nights. Objective sleep parameters were assessed using actigraphy, while subjective sleep quality was evaluated using validated self-report measures. Training load, perceptual factors, pre-sleep nutrition, and nocturnal thermal conditions were monitored and controlled to limit potential confounding factors. The primary objective was to determine whether nocturnal compression garment use affects sleep quantity and quality in young elite soccer players.

Descripción general del estudio

Estado

Terminado

Condiciones

Descripción detallada

This randomized controlled crossover study was conducted in young elite male soccer players from a professional soccer club academy to investigate the effects of nocturnal compression garments on sleep quantity and quality.

The study was conducted over four consecutive weeks. During the first week, all participants completed a baseline control condition without wearing any garment during the night. This baseline condition was always performed first and was not randomized. During the following three weeks, participants completed three garment conditions in a randomized order: full-length compression leggings, compression calf sleeves, and non-compressive placebo garments. Each condition was maintained for seven consecutive nights.

Participants were instructed to put on the assigned garment approximately two hours before bedtime, wear it throughout the night, and remove it after waking. The placebo garment was designed to provide a similar wearing experience without applying meaningful compression.

Sleep was assessed objectively using wrist actigraphy and subjectively using self-reported sleep measures. Objective sleep variables included total sleep time, time in bed, sleep latency, sleep efficiency, and the number of nocturnal awakenings.

To limit potential confounding factors, external and internal training loads, perceived stress, fatigue and muscle soreness, pre-sleep nutritional intake, and nocturnal thermal conditions were monitored throughout the experimental period. The study was conducted under standardized living and training conditions within the professional soccer academy environment.

Tipo de estudio

Intervencionista

Inscripción (Actual)

18

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

      • Avion, Francia, 62210
        • Centre technique et sportif de la Gaillette Gervais Martel

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
  • Adulto

Acepta Voluntarios Saludables

Sí

Descripción

Inclusion Criteria:

  • Residence at the professional soccer academy throughout the study period.
  • Abstinence from tobacco and alcohol throughout the study period.
  • No caffeine intake within 12 hours before bedtime.
  • Absence of sleep deficit at inclusion.
  • Absence of illness at inclusion.

Exclusion Criteria:

  • Sustaining an injury during the study period.
  • Exposure to a training load substantially different from that of the rest of the group.
  • Development or presence of a sleep deficit during the study period.
  • Failure to consume the standardized evening meal provided at the academy cafeteria.
  • Consumption of caffeine, tobacco, or alcohol during the study period.
  • Removal of the assigned garment or actigraphy device during the night.

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 cruzada
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Sequence 1: Leggings - Calf Sleeves - Placebo
Participants wore fullcompression leggings from approximately two hours before bedtime until waking for seven consecutive nights.
Participants wore compression calf sleeves from approximately two hours before bedtime until waking for seven consecutive nights.
Participants wore visually similar non-compressive placebo garments from approximately two hours before bedtime until waking for seven consecutive nights.
Experimental: Sequence 2: Calf Sleeves - Placebo - Leggings
Participants wore fullcompression leggings from approximately two hours before bedtime until waking for seven consecutive nights.
Participants wore compression calf sleeves from approximately two hours before bedtime until waking for seven consecutive nights.
Participants wore visually similar non-compressive placebo garments from approximately two hours before bedtime until waking for seven consecutive nights.
Experimental: Sequence 3: Placebo - Leggings - Calf Sleeves
Participants wore fullcompression leggings from approximately two hours before bedtime until waking for seven consecutive nights.
Participants wore compression calf sleeves from approximately two hours before bedtime until waking for seven consecutive nights.
Participants wore visually similar non-compressive placebo garments from approximately two hours before bedtime until waking for seven consecutive nights.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Total Sleep Time
Periodo de tiempo: Assessed nightly during each 7-night condition
Assessed nightly during each 7-night condition
Time in Bed
Periodo de tiempo: Assessed nightly during each 7-night condition
Assessed nightly during each 7-night condition
Sleep Latency
Periodo de tiempo: Assessed nightly during each 7-night condition
Assessed nightly during each 7-night condition
Mean Sleep Efficiency Assessed by Wrist Actigraphy
Periodo de tiempo: Measured nightly and averaged across the 7 consecutive nights of each condition
Sleep efficiency was assessed by wrist actigraphy and calculated as the percentage of time in bed spent asleep. Nightly sleep efficiency values were averaged across the seven consecutive nights of each experimental condition. Higher values indicate greater sleep efficiency.
Measured nightly and averaged across the 7 consecutive nights of each condition
Number of Nocturnal Awakenings
Periodo de tiempo: Assessed nightly during each 7-night condition
Assessed nightly during each 7-night condition
Subjective Sleep Quality Assessed Using the Sleep Item of the Hooper Questionnaire
Periodo de tiempo: Assessed nightly during each 7-night condition
Subjective sleep quality was assessed using the sleep-quality item of the Hooper Questionnaire (Hooper et al., 1995). Participants rated the quality of the previous night's sleep on a 7-point Likert-type scale ranging from 1 (very, very good) to 7 (very, very bad), with higher scores indicating poorer perceived sleep quality.
Assessed nightly during each 7-night condition

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)

2 de noviembre de 2025

Finalización primaria (Actual)

14 de diciembre de 2025

Finalización del estudio (Actual)

14 de diciembre de 2025

Fechas de registro del estudio

Enviado por primera vez

25 de agosto de 2026

Primero enviado que cumplió con los criterios de control de calidad

30 de agosto de 2026

Publicado por primera vez (Actual)

3 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

3 de septiembre de 2026

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

30 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • UPJV-COMP-SLEEP-01
  • 2024-10-1/2024-46 (Otro identificador: Comité d'éthique pour les recherches non interventionnelles (CERNI), Université de Picardie Jules Verne)

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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