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A Study on the Effects of Instability Resistance Training on Dynamic Balance and Rapid Change-of-Direction Ability in College Basketball Recruits

6 de julio de 2026 actualizado por: Richen Sun

The Effects of Unstable Resistance Training on Dynamic Balance and Rapid Change-of-Direction Ability in Male College Basketball Players: A Randomized Controlled Trial

This experiment aims to investigate the effects of unstable resistance training on the dynamic balance ability and rapid directional change mobility of college basketball majors, while comparing it with traditional resistance training to analyze the statistical differences between the two in enhancing the dynamic balance ability and rapid directional change mobility of the majors-Parazacco spilurus subsp. spilurus-and to explore the underlying reasons, thereby opening new research avenues for improving the dynamic balance ability and rapid directional change mobility of college majors.

Descripción general del estudio

Descripción detallada

All participants completed a 12-week training program, training three times per week with at least a 48-hour interval between consecutive training sessions. Depending on their group assignment, participants performed either unstable resistance training (experimental group) or traditional resistance training on a stable surface (control group). Both groups followed the same training frequency, training volume, exercise sequence, and rest intervals between sets; the only difference was the training surface. During training, the experimental group used unstable equipment such as BOSU balls, balance pads, and Swiss balls, while the control group performed the corresponding exercises on a stable floor. All training sessions were uniformly supervised by researchers to ensure proper form and training adherence.

Each training session began with a standardized warm-up, including 5 minutes of light jogging and dynamic stretching, followed by exercise-specific warm-up movements. Prior to the formal training, participants completed one set of adaptation exercises at approximately 50% of the formal training load. Rest periods between exercises were 30 seconds, while rest periods between sets were controlled at 45-60 seconds depending on the training phase.

The experimental group's training program was divided into three cycles. Weeks 1 through 4 constituted the basic adaptation phase, with training consisting of BOSU ball elbow plank (40 s × 4 sets), squats on a balance pad (10 reps × 4 sets), back-against-Swiss-ball squats with ball between the knees (40 s × 4 sets), and swan-pose balance on the BOSU ball (30 s × 4 sets), with 45 s of rest between sets. Weeks 5 through 8 constitute the enhancement phase, with training consisting of weighted squats on a balance pad (15 reps × 4 sets), weighted deadlifts on a balance pad (10 reps × 4 sets), alternating lunges on a BOSU ball (15 reps × 4 sets), and medicine ball lunge twists with toss and catch (with the front leg on the BOSU ball) (12 reps × 4 sets), with a 45-second rest between sets. Weeks 9 through 12 constitute the consolidation phase, with training consisting of weighted single-leg deadlifts on a balance pad (12 reps × 4 sets), weighted crunches on a BOSU ball (12 reps × 4 sets), weighted Russian twists on the BOSU ball (12 reps × 4 sets), and weighted Bulgarian split squats on the BOSU ball (12 reps × 4 sets), with 60 s of rest between sets.

The control group underwent traditional resistance training on a stable surface, with the same training cycle and training volume as the experimental group. Weeks 1 through 4 consisted of elbow plank (40 s × 4 sets), single-leg lifts on a flat surface (10 reps × 4 sets), static squats with a ball held against a wall (40 s × 4 sets), and swan pose balance on the floor (30 s × 4 sets); Weeks 5 through 8: squats (15 reps × 4 sets), weighted single-leg lifts (10 reps × 4 sets), weighted alternating lunges (15 reps × 4 sets), and medicine ball lunge twists with toss and catch (12 reps × 4 sets); Weeks 9 through 12 consisted of weighted squats (12 reps × 4 sets), weighted crunches (12 reps × 4 sets), weighted Russian twists (12 reps × 4 sets), and weighted Bulgarian split squats (12 reps × 4 sets), with rest intervals of 45 s and 60 s between sets, respectively. The experimental instruments and their models used during the experiment were as follows: stopwatch (PC2810, China), measuring tape (JGW-5m, China) , a whistle (PE-001, China), marker cones (KS-TC23, China), a Y Balance Test Kit™ (USA), a BOSU ball (SH-BOSU58, China), a balance mat (SH-BP34, China), 5 kg dumbbells (SH-DB5, China), a 5 kg medicine ball (SH-MB5, China), barbell plates (SH-WP5, China), and 65 cm Swiss balls (SH-GB65, China).

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

    • Guangdong
      • Guangzhou, Guangdong, Porcelana, 510630
        • Guangzhou Sports University Indoor Basketball Gymnasium

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
  • Adulto Mayor

Acepta Voluntarios Saludables

Sí

Descripción

Inclusion Criteria:

  • Students in the specialized basketball class.
  • No history of sports-related injuries in the past six months.
  • No history of serious injuries or illnesses that would affect participation in this experiment.
  • Willing to participate in the experiment and have signed an informed consent form.

Exclusion Criteria:

  • History of surgery on the upper or lower limbs or other parts of the body within the past six months.
  • History of severe sports injuries or physical illnesses.

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 paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Unstable Resistance Training Group
Unstable Resistance Training Intervention. The training program primarily consists of unstable resistance squats and unstable planks. Depending on the participants' fitness levels and safety considerations, the program is supplemented with auxiliary exercises and sport-specific warm-ups. During training, relevant information such as compliance, number of sets, number of repetitions, subjective effort perception, attendance, and adverse events is recorded.
Unstable Resistance Training Intervention. The training program primarily consists of unstable resistance squats and unstable planks. Depending on the participants' fitness levels and safety considerations, the program is supplemented with auxiliary exercises and sport-specific warm-ups. During training, relevant information such as compliance, number of sets, number of repetitions, subjective effort perception, attendance, and adverse events is recorded.
Otro: Traditional Resistance Training Group
Traditional resistance training. This primarily involves exercises such as squats and planks, without the use of equipment like stability balls that promote instability.
Traditional resistance training. This primarily involves exercises such as squats and planks, without the use of equipment like stability balls that promote instability.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change from baseline in normalized Y-Balance Test composite score after 12 weeks of training
Periodo de tiempo: Day 0, Day 74
The Y-Balance Test will be used to evaluate lower-limb dynamic balance. Reach distances in the anterior, posteromedial, and posterolateral directions will be measured for both the left and right limbs. All reach distances will be normalized to limb length, and a composite score will be calculated for each limb. The primary reported value will be the change in normalized composite score from baseline to 12 weeks. Higher values represent better dynamic balance ability.
Day 0, Day 74

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change from baseline in Illinois Agility Test completion time after 12 weeks of training
Periodo de tiempo: Day 0, Day 74
The Illinois Agility Test will be used to assess change-of-direction speed and agility performance. Participants will complete the standardized Illinois Agility Test course consisting of straight-line sprinting and multiple changes of direction around cones. Completion time will be recorded in seconds using a stopwatch. Two trials will be performed, and the fastest completion time will be used for analysis. The primary reported outcome will be the change in completion time from baseline to 12 weeks. Lower completion times indicate better change-of-direction performance.
Day 0, Day 74
Change from baseline in Pro Agility Test completion time after 12 weeks of training
Periodo de tiempo: Day 0, Day 74
The Pro Agility Test (5-10-5 shuttle run) will be used to assess multidirectional change-of-direction speed and agility. Participants will sprint 5 m to one side, change direction to sprint 10 m in the opposite direction, and then change direction again to sprint 5 m back through the starting line. Completion time will be recorded in seconds using a stopwatch. Two trials will be performed, and the fastest completion time will be used for analysis. The primary reported outcome will be the change in completion time from baseline to 12 weeks. Lower completion times indicate better change-of-direction performance.
Day 0, Day 74
Change from baseline in Nebraska Agility Test completion time after 12 weeks of training
Periodo de tiempo: Day 0, Day 74
The Nebraska Agility Test will be used to assess multidirectional agility, change-of-direction speed, and body control. Participants will complete the standardized Nebraska Agility Test course, which includes sprinting, lateral shuffling, backward running, turning, and rapid directional changes around designated cones. Completion time will be recorded in seconds using a stopwatch. Two trials will be performed, and the fastest completion time will be used for analysis. The primary reported outcome will be the change in completion time from baseline to 12 weeks. Lower completion times indicate better agility and change-of-direction performance.
Day 0, Day 74
Change from baseline in Three-Second Zone Multi-directional Movement Test completion time after 12 weeks of training
Periodo de tiempo: Day 0, Day 74
The Three-Second Zone Multi-directional Movement Test will be used to assess basketball-specific multidirectional movement ability, including sprinting, lateral shuffling, backward running, and rapid changes of direction. Participants will complete the standardized movement course within the basketball three-second zone. Completion time will be recorded in seconds using a stopwatch. Two trials will be performed, and the fastest completion time will be used for analysis. The primary reported outcome will be the change in completion time from baseline to 12 weeks. Lower completion times indicate better multidirectional movement and change-of-direction performance.
Day 0, Day 74
Change from baseline in T-Test completion time after 12 weeks of training
Periodo de tiempo: Day 0, Day 74
The T-Test will be used to assess agility, multidirectional movement, and change-of-direction speed. Participants will complete the standardized T-Test course, which includes forward sprinting, lateral shuffling to both directions, and backward running. Completion time will be recorded in seconds using a stopwatch. Two trials will be performed, and the fastest completion time will be used for analysis. The primary reported outcome will be the change in completion time from baseline to 12 weeks. Lower completion times indicate better agility and change-of-direction performance.
Day 0, Day 74

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Director de estudio: Hengtong Wang, Ph.D., Professor, Guangzhou sport univeristy

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.

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 marzo de 2025

Finalización primaria (Actual)

30 de junio de 2025

Finalización del estudio (Actual)

30 de junio de 2025

Fechas de registro del estudio

Enviado por primera vez

25 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

6 de julio de 2026

Publicado por primera vez (Actual)

10 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

10 de julio de 2026

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

6 de julio de 2026

Última verificación

1 de julio de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • 2024LCLL-149

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

Due to the need to protect the privacy of the study participants, the experimental data will not be made public; however, if necessary, please contact the author for reasonable use.

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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