Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

Low-Load BFR vs. High-Load Training on Biceps Hypertrophy

2 de mayo de 2026 actualizado por: Huseyin Sahin UYSAL, Mehmet Akif Ersoy University

Bayesian Comparison of Low-Load Blood Flow Restriction and High-Load Resistance Exercise on Biceps Brachii Muscle Hypertrophy in Untrained Men

This study aimed to compare the effects of low-load blood flow restriction resistance exercise (BFR-RE) performed to voluntary failure with traditional high-load resistance exercise (HL-RE) and a control condition on biceps brachii muscle hypertrophy, muscle stiffness, and maximal strength in untrained young men.

Participants completed an 8-week training program, with exercise performed three times per week. Outcomes were assessed using ultrasound imaging, elastography, and one-repetition maximum (1RM) testing. The study evaluates whether low-load BFR training can produce adaptations comparable to high-load resistance training.

Descripción general del estudio

Descripción detallada

This study was designed to examine the efficacy of low-load blood flow restriction resistance exercise (BFR-RE) performed to voluntary failure compared with traditional high-load resistance exercise (HL-RE) in inducing muscular adaptations in untrained individuals. The experimental framework was structured to isolate the effects of mechanical load and metabolic stress by standardizing the selection of exercises and the training frequency across groups.

A controlled, single-blind, repeated-measures design was used, with participants allocated to BFR-RE, HL-RE, or a non-exercising control condition. The intervention period was set at 8 weeks to ensure sufficient exposure for hypertrophic and neuromuscular adaptations, while minimizing potential confounding effects of long-term training variability.

The BFR-RE protocol was developed to emphasize metabolic stress through low external loading (30% 1RM), partial vascular occlusion (60% limb occlusion pressure), and sets performed to volitional failure. In contrast, the HL-RE condition was structured to prioritize mechanical tension using moderate-to-high loading (70% 1RM) without vascular restriction. This contrast enables a mechanistic comparison of two distinct hypertrophic stimuli.

To reduce acute exercise-induced confounding factors, particularly transient muscle swelling, post-intervention assessments were complemented with a delayed follow-up measurement. This approach was incorporated better to reflect true morphological adaptations rather than short-term physiological responses.

The methodological approach integrates imaging-based and performance-based assessments to capture both structural and functional adaptations. The overall design enables evaluation of whether BFR-RE can provide a time-efficient and lower-load alternative to traditional resistance training while maintaining comparable adaptive outcomes.

Tipo de estudio

Intervencionista

Inscripción (Actual)

33

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

    • Karabük Province
      • Karabük, Karabük Province, Turquía (Türkiye), 78050
        • Karabük University Hasan Dogan Faculty of Sport Sciences

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:

Healthy male participants aged 18-30 years No prior history of structured or specialized resistance training targeting the biceps brachii muscle Normotensive (blood pressure <140/90 mmHg) Right-handed (to reduce variability related to limb dominance) Willing to provide written informed consent and comply with the study protocol

Exclusion Criteria:

History of orthopedic injury or musculoskeletal disorder affecting the upper extremities Diagnosis of hypertension (≥140/90 mmHg) or cardiovascular disease Any neurological condition affecting motor performance Current participation in any structured resistance training program Use of medications or supplements known to influence muscle metabolism or performance

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: No aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: BFR-RE
Participants performed low-load resistance exercise with blood flow restriction using 30% of one-repetition maximum (1RM) and 60% limb occlusion pressure. Exercises were performed to voluntary failure, three times per week for 8 weeks.
Resistance exercise was performed under partial vascular occlusion using a pneumatic cuff applied to the upper arm. Limb occlusion pressure was individually determined, and exercise was conducted at a relative intensity corresponding to a percentage of one-repetition maximum. Occlusion pressure was maintained during sets and released between exercises. Training load and repetition tempo were standardized and progressively adjusted throughout the intervention period.
Otros nombres:
  • Entrenamiento BFR
Comparador activo: HL-RE
Participants performed traditional high-load resistance exercise at 70% of one-repetition maximum (1RM) without blood flow restriction, three times per week for 8 weeks.
Participants performed resistance exercise using conventional loading strategies based on a percentage of one-repetition maximum. Training intensity, volume, and progression were standardized across sessions, with loads adjusted periodically according to performance assessments.
Otros nombres:
  • Traditional Resistance Training
Sin intervención: Control
Participants did not engage in any structured resistance training program and continued their normal daily activities throughout the 8-week study period.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Biceps Brachii Muscle Thickness
Periodo de tiempo: Baseline and 8 weeks (post-intervention), with an additional follow-up measurement at 1 week after the intervention
Muscle thickness of the biceps brachii was assessed using ultrasound imaging to evaluate hypertrophic adaptations following the intervention.
Baseline and 8 weeks (post-intervention), with an additional follow-up measurement at 1 week after the 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)

1 de junio de 2025

Finalización primaria (Actual)

3 de agosto de 2025

Finalización del estudio (Actual)

3 de agosto de 2025

Fechas de registro del estudio

Enviado por primera vez

24 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

24 de abril de 2026

Publicado por primera vez (Actual)

1 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

7 de mayo de 2026

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

2 de mayo de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • Mehmet Akif Ersoy Universitesi
  • BFR_HLRE_UntrainedMen (Identificador de registro: Bayesian Comparison of Low-Load Blood Flow Restriction and High-Load Resistance Exercise on Biceps Brachii Muscle Hyper)

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. .

Suscribir