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Cluster Training With Blood Flow Restriction in Competitive 200-m Freestyle Swimmers (BFR-CLUSTER-SW)

24 de agosto de 2026 actualizado por: Saif Rasheed Ghanim

Cluster Training With Blood Flow Restriction and 200-m Freestyle Performance, FGF-2, and VEGF-A Responses in Competitive Swimmers: A Matched Controlled Study

This study evaluated whether adding blood flow restriction (BFR) to cluster-based training could improve swimming performance and selected physiological responses in competitive swimmers. Twenty competitive swimmers were assigned using a matched, non-randomized design to either an experimental group performing cluster training combined with BFR or a control group performing the same cluster training without BFR. The intervention lasted 8 weeks, with five training sessions per week. The primary outcome was 200-m freestyle performance time. Secondary outcomes included serum concentrations of fibroblast growth factor-2 (FGF-2) and vascular endothelial growth factor-A (VEGF-A), standing long jump performance, mean 50-m split time during a 150-m swimming test, and repetitions completed during a cadence-controlled Burpee test. The study was designed to determine whether BFR provided additional performance and physiological benefits beyond cluster training alone.

Descripción general del estudio

Estado

Terminado

Condiciones

Intervención / Tratamiento

Descripción detallada

Blood flow restriction (BFR) training is a training method in which pneumatic cuffs are applied proximally to the limbs to partially restrict vascular flow during exercise. Cluster training divides traditional exercise sets into smaller clusters of repetitions separated by short intra-set recovery periods. Combining these two approaches may increase the physiological stimulus of training while allowing repeated high-quality exercise efforts.

This controlled, non-randomized matched-intervention study included 20 competitive 200-m freestyle swimmers. Participants were matched according to baseline 200-m freestyle performance, sex, and standing long jump distance and were assigned to one of two groups. The experimental group completed cluster training combined with BFR, whereas the control group completed cluster training without BFR.

The training intervention lasted 8 weeks and consisted of five 90-minute training sessions per week. Sessions included a standardized warm-up, a main training component, and a cool-down. Overall cardiovascular training intensity was prescribed relative to individual maximal heart rate, and cluster-based resistance exercises incorporated short intra-set recovery intervals.

BFR was applied only in the experimental group during selected dry-land cluster exercises using pneumatic cuffs positioned proximally on the upper arms and thighs. The cuffs remained inflated during exercise execution and short intra-set recovery periods and were deflated during the main inter-set recovery periods.

The primary outcome was change in 200-m freestyle performance time from baseline to the end of the 8-week intervention. Secondary outcomes included serum FGF-2 and VEGF-A concentrations, standing long jump distance, mean 50-m split time during a maximal 150-m swimming test, and performance in a cadence-controlled Burpee test. Blood samples were collected under standardized resting conditions to assess serum FGF-2 and VEGF-A concentrations.

The main objective was to determine whether the addition of BFR to cluster training was associated with greater improvements in swimming performance, selected physical-performance outcomes, and serum angiogenesis-related biomarkers compared with cluster training alone.

Tipo de estudio

Intervencionista

Inscripción (Actual)

20

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

    • Muhafazat Salah ad Din
      • Samarra, Muhafazat Salah ad Din, Irak, 34010
        • Samarra Olympic Swimming Pool

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:

Competitive 200-m freestyle swimmers aged 17-20 years. At least 2 years of structured swimming training experience. Free from musculoskeletal injury for at least 6 months before enrollment. No previous regular experience with blood flow restriction training. Willing and able to complete the 8-week training intervention and all study assessments.

Exclusion Criteria:

History of cardiovascular, metabolic, thrombotic, or other vascular conditions that could contraindicate blood flow restriction exercise.

Current use of medications known to affect vascular tone or blood coagulation. Musculoskeletal injury or medical condition preventing participation in maximal swimming or dry-land training.

Attendance below 85% of the scheduled intervention sessions.

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

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Cluster Training With Blood Flow Restriction
Participants in this arm completed an 8-week cluster-training program combined with blood flow restriction (BFR). Training was performed five sessions per week. Pneumatic cuffs were applied proximally to the upper arms and thighs during selected dry-land cluster exercises and intra-set recovery periods, and were deflated during the main inter-set recovery periods.
An 8-week cluster-training program performed five sessions per week, with blood flow restriction applied during selected dry-land cluster exercises using pneumatic cuffs positioned proximally on the upper arms and thighs.
Comparador activo: Cluster Training Alone
Participants in this arm completed the same 8-week cluster-training program and overall training schedule as the experimental group, but without blood flow restriction. Training was performed five sessions per week.
An 8-week cluster-training program performed five sessions per week without blood flow restriction.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in 200-m Freestyle Performance Time
Periodo de tiempo: Baseline and post-intervention at 8 weeks
Performance was assessed during a maximal 200-m freestyle swim in a standard 50-m pool using an electronic timing system with a precision of 0.01 s. Lower values indicate faster performance. The primary outcome was the change in performance time from baseline to the end of the 8-week intervention.
Baseline and post-intervention at 8 weeks

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 (Actual)

15 de enero de 2026

Finalización primaria (Actual)

19 de marzo de 2026

Finalización del estudio (Actual)

15 de junio de 2026

Fechas de registro del estudio

Enviado por primera vez

21 de agosto de 2026

Primero enviado que cumplió con los criterios de control de calidad

21 de agosto de 2026

Publicado por primera vez (Actual)

25 de agosto de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

26 de agosto de 2026

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

24 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • SRG-BFR-SWIM-2026-01

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. .