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Isokinetic Knee Strength, Bilateral Muscle Balance, and Anaerobic Performance in Adolescent Athletes (ISOK-WAnT)

2 de noviembre de 2026 actualizado por: Assoc. Prof. Dr. Özgür EKEN, Inonu University

Relationship of Isokinetic Knee Strength and Bilateral Muscle Balance With Anaerobic Performance in Adolescent Athletes

This study looks at how strong the knee muscles are in adolescent athletes and how this strength relates to short-term, high-intensity (anaerobic) performance. Strong, well-balanced thigh muscles may help athletes produce more power during sport movements, but this has not been studied well in teenagers. Male athletes aged 15-16 years will be measured on two separate days. On the first day, their height and body weight will be measured and the strength of the muscles at the front (quadriceps) and back (hamstrings) of both thighs will be tested on a special strength-testing machine. On the second day, they will do a 30-second all-out cycling test to measure anaerobic power. The study will compare the right and left legs and will examine whether knee muscle strength and the balance between the front and back thigh muscles are linked to power output during the cycling test. No treatment or intervention will be given. The results may help coaches and sports scientists understand the physical development of adolescent athletes.

Descripción general del estudio

Descripción detallada

Lower-limb strength and anaerobic power are important parts of the physical profile of adolescent athletes in high-intensity sports such as wrestling. Isokinetic dynamometry allows knee extensor (quadriceps) and flexor (hamstring) strength and the balance between these muscle groups to be measured objectively, while the 30-second Wingate Anaerobic Test (WAnT) is a widely used laboratory test of anaerobic performance. Evidence on how these measures relate to each other in adolescent athletes is limited.

This is a cross-sectional, correlational observational study. Twenty-one male adolescent athletes aged 15-16 years will be recruited in Malatya, Turkey. Written informed consent will be obtained from parents or legal guardians, and assent from participants. Testing will take place on two separate days to limit fatigue. Participants will avoid heavy exercise for 48 hours and caffeine for 12 hours before testing.

Day 1: Height and body mass are measured and body mass index is calculated. Concentric knee extension and flexion are then tested bilaterally on a HUMAC NORM isokinetic dynamometer at 60, 120 and 180 degrees per second (three practice repetitions followed by five maximal repetitions at each speed; 45 seconds of rest between speeds and 10 minutes between limbs). Peak torque is recorded for the quadriceps and hamstrings of each limb, and the conventional hamstring-to-quadriceps (H/Q) ratio is calculated.

Day 2: Participants complete a 30-second WAnT on a mechanically braked cycle ergometer (Monark 874E) with a braking load of 0.075 kg per kg of body mass, after a standardized warm-up. Peak power, mean power and fatigue index are recorded.

Differences between the right and left limbs will be examined with paired-samples t-tests (with 95% confidence intervals and Cohen's dz). Associations between isokinetic variables and WAnT outcomes will be examined with Pearson correlation. The sample size (minimum 19) was calculated with G*Power for a correlation of r = 0.60 (alpha = 0.05, power = 0.80); 21 participants are planned to allow for possible data loss.

Tipo de estudio

De observación

Inscripción (Estimado)

21

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

  • Nombre: Ozgur Eken, PhD, Associate Professor
  • Número de teléfono: +90 553 213 27 95
  • Correo electrónico: ozgur.eken@inonu.edu.tr

Copia de seguridad de contactos de estudio

Ubicaciones de estudio

    • Malatya
      • Malatya, Malatya, Turquía (Türkiye), 44280
        • Department of Physical Education and Sport Teaching, Faculty of Sports Sciences, Inonu University,
        • Contacto:
        • Contacto:
        • Investigador principal:
          • Özgür Eken, PhD, Assoc. Prof
        • Sub-Investigador:
          • Denizhan Caliskan, Dr.

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

15 años a 16 años (Niño)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Masculino

Método de muestreo

Muestra no probabilística

Población de estudio

Male adolescent athletes aged 15-16 years who actively wrestle and train regularly in Malatya, Turkey. Participants are healthy athletes recruited from local clubs on a voluntary basis.

Descripción

Inclusion Criteria:

  • Actively practicing wrestling in Malatya, Turkey
  • Male, aged 15-16 years
  • At least 2 years of regular training (at least 2 days per week)
  • No lower-extremity injury or surgery in the last 6 months
  • No musculoskeletal, cardiometabolic, or neurological condition that could prevent testing
  • Willing to participate in all planned tests
  • Written informed consent signed by parent or legal guardian, and assent from the participant

Exclusion Criteria: * Younger than 15 or older than 16 years

  • Lower-extremity injury or surgery within the last 6 months
  • Musculoskeletal, cardiometabolic, or neurological condition that could prevent testing
  • Open wound, varicose veins, acute inflammation, or history of thrombosis
  • Regular use of analgesic or anti-inflammatory medication or ergogenic supplements in the last 3 months
  • Unable to attend all planned testing sessions
  • Unwilling to follow the pre-test rules (no heavy exercise for 48 hours, no caffeine for 12 hours, usual training and diet)
  • Withdrawal during the study due to non-compliance, incomplete sessions, serious injury or illness, or participant request

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

  • Modelos observacionales: COHORT
  • Perspectivas temporales: CROSS_SECTIONAL

Cohortes e Intervenciones

Grupo / Cohorte
Intervención / Tratamiento
Adolescent Athletes

Male adolescent athletes aged 15-16 years who regularly train and compete. All participants complete anthropometric measurements, bilateral isokinetic knee strength testing, and the Wingate Anaerobic Test on separate days.

Bilateral concentric knee extension and flexion tested on an isokinetic dynamometer at 60, 120, and 180 degrees per second. Peak torque and the conventional hamstring-to-quadriceps ratio are recorded.

A 30-second all-out cycling test on a mechanically braked cycle ergometer with a braking load of 0.075 kg per kg of body mass. Peak power, mean power, and fatigue index are recorded.

Otros nombres:
  • WAnT

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Isokinetic Peak Torque of the Knee Extensors and Flexors
Periodo de tiempo: Day 1 of testing (single measurement session)

Peak torque (N·m) of the quadriceps and hamstrings, measured separately for the right and left limbs at 60, 120, and 180 degrees per second on an isokinetic dynamometer (highest value across five maximal concentric repetitions). Right-to-left differences and associations with Wingate Anaerobic Test outcomes are analyzed.

Day 1 of testing (single measurement session)
Wingate Anaerobic Test Peak Power
Periodo de tiempo: Day 2 of testing (single measurement session)

Highest power output (W) achieved during the 30-second Wingate Anaerobic Test performed on a mechanically braked cycle ergometer with a braking load of 0.075 kg per kg of body mass.

Day 2 of testing (single measurement session)

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Conventional Hamstring-to-Quadriceps (H/Q) Strength Ratio
Periodo de tiempo: Day 1 of testing

Concentric hamstring peak torque divided by quadriceps peak torque, multiplied by 100 (%), calculated for each limb at 60, 120, and 180 degrees per second.

Day 1 of testing
Wingate Anaerobic Test Mean Power
Periodo de tiempo: Day 2 of testing

Average power output (W) maintained across the 30-second Wingate Anaerobic Test.

Day 2 of testing
Wingate Anaerobic Test Fatigue Index
Periodo de tiempo: Day 2 of testing

Percentage decline from peak power to the lowest power output during the test: [(peak power - minimum power) / peak power] × 100.

Day 2 of testing

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Investigador principal: Özgür Eken, PhD, Assoc. Prof., Inonu University, Faculty of Sport Sciences
  • Director de estudio: Denizhan Çalışkan, Dr., Eskisehir Provincial Directorate of Youth and Sports, Eskisehir, Türkiye

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.

Publicaciones Generales

  • Aagaard, P., Simonsen, E. B., Magnusson, S. P., Larsson, B., & Dyhre-Poulsen, P. (1998). A new concept for isokinetic hamstring:quadriceps muscle strength ratio. The American Journal of Sports Medicine, 26(2), 231-237. Alemdaroğlu, U. (2012). The relationship between muscle strength, anaerobic performance, agility, sprint ability and vertical jump performance in professional basketball players. Journal of Human Kinetics, 31, 149-158. Chaabene, H., Negra, Y., Bouguezzi, R., Capranica, L., Franchini, E., Prieske, O., Hbacha, H., & Granacher, U. (2017). Physical and physiological attributes of wrestlers: An update. Journal of Strength and Conditioning Research, 31(5), 1411-1442. Iossifidou, A., Baltzopoulos, V., & Giakas, G. (2005). Isokinetic knee extension and vertical jumping: Are they related? Journal of Sports Sciences, 23(9), 1121-1127.

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)

28 de diciembre de 2026

Finalización primaria (Estimado)

28 de enero de 2027

Finalización del estudio (Estimado)

28 de enero de 2027

Fechas de registro del estudio

Enviado por primera vez

2 de noviembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

2 de noviembre de 2026

Publicado por primera vez (Actual)

6 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

6 de noviembre de 2026

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

2 de noviembre de 2026

Última verificación

1 de noviembre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • INONU-ISOKINETIC-2026-01
  • IKINETIK-WAnT-2026 (Otro identificador: Inonu University)

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 shared, because participants are minors and the consent forms state that data will be used only for the purposes of this research and kept confidential. Aggregate results will be published.

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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