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Impact of Abdominal Muscle-Induced Fatigue on Hip Muscle Performance and Functional Balance in Healthy Adults

5 de mayo de 2026 actualizado por: Ahmed Samir Abdellatif, Cairo University

The study is based on the theory that the abdominal muscles contribute to transverse and frontal plane torques that complement hip abductor torque, as both muscle groups act in the same counterclockwise direction within the proposed biomechanical model. Through their role in trunk and pelvic stabilization, the abdominal muscles help optimize the mechanical environment in which the hip abductors operate, potentially enhancing their effective torque production during functional tasks.

This shared torque direction suggests a functional interdependence between core and hip musculature, whereby deficits or fatigue in the abdominal muscles may compromise hip abductor performance and load distribution at the hip joint. Clinically, this relationship supports the integration of abdominal muscle assessment and targeted core rehabilitation into the evaluation and management of hip-related injuries, with the potential to improve movement control, reduce injury risk, and enhance treatment outcomes. A quasi-experimental, within-subject study conducted at the Isokinetic Laboratory, Faculty of Physical Therapy, Cairo University, to examine the effect of abdominal muscle-induced fatigue on hip muscle strength, endurance, and functional balance. Seventy healthy male college students aged 20-25 years will be assessed before and after an isokinetic abdominal fatigue protocol using an isokinetic dynamometer. Outcome measures include isokinetic hip muscle strength and endurance, as well as balance assessed by the Single Leg Stance Test and Star Excursion Balance Test. The study procedure consists of participant preparation, baseline assessment, abdominal muscle fatigue induction, and immediate post-fatigue reassessment. Sample size was determined using G*Power to ensure adequate statistical power, and data will be analyzed using one-way within-subject MANOVA with significance set at p < 0.05. This study holds critical importance for advancing both biomechanical theory and clinical practice by directly investigating a key, yet under-quantified, link in the human kinetic chain: the specific impact of abdominal muscle fatigue on hip muscle performance and functional balance. By employing instrumented (Isokinetic dynamometer, star excursion balance test and single leg stance test)., pre- and post-fatigue measurements in a healthy non-athletic population, it will generate novel empirical evidence clarifying how core endurance directly influences proximal stability and distal function. Clinically, the outcomes promise to transform assessment and rehabilitation paradigms-shifting focus from isolated hip treatment toward integrated core-hip strategies-ultimately informing more effective injury prevention programs, optimizing movement efficiency, and enhancing rehabilitation outcomes for both athletic and general populations.

Descripción general del estudio

Tipo de estudio

De observación

Inscripción (Estimado)

70

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: Ahmed Samir Abdel Latif, MSc in Biomechanics
  • Número de teléfono: 01222832888
  • Correo electrónico: ahmedsamir9430@gmail.com

Ubicaciones de estudio

    • Giza Governorate
      • Giza, Giza Governorate, Egipto, 12534
        • Degla Palms
        • Contacto:
          • Ahmed Samir Abdel Latif, MSc in Biomechanics
          • Número de teléfono: 01222832888
          • Correo electrónico: ahmedsamir9430@gmail.com

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

Método de muestreo

Muestra no probabilística

Población de estudio

The study population consists of 70 healthy, non-athletic students aged between 20 and 25 years. These participants were specifically selected to maintain homogeneity in the data, ensuring they possess the necessary physical capacity to perform the required isokinetic contractions and manual muscle tests while remaining free from recent injury, musculoskeletal pain, or neurological conditions that could compromise the accuracy of the balance and strength assessments.

Descripción

Inclusion Criteria:

  • Healthy colleague male students aged 20-25 years (Cerda et al., 2018).
  • No history of low back, hip, knee or pelvic surgery in past year (Hietamo et al., 2021).
  • Physically able to perform isokinetic contractions against isokinetic dynamometer (Babiloni et al., 2025).
  • Body mass index (BMI) from 18 to 25 (Milanese et al., 2025).
  • Abdominal and Hip manual muscle test of 4 or above (Ciesla et al.,2011).

Exclusion Criteria:

  • Current musculoskeletal pain in trunk, hip, or lower limb (Hietamo et al., 2021).
  • Neurological disorders affecting balance (e.g vertebra basilar insufficiency) or muscle performance (Pongmala et al., 2024).
  • Recent participation (48-72 h) in strenuous trunk/hip exercise that might confound fatigue measures (Foucher et al., 2021).
  • Participation in athletic activities (Elliott et al., 2021).

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

Cohortes e Intervenciones

Grupo / Cohorte
Intervención / Tratamiento
Study Group
Seventy healthy colleague students aged from 20 to 25 will participate in this study, they will all be placed in one group that will be tested before and after the abdominal muscle fatigue protocol for their hip muscle strength, endurance using Isokinetic dynamometer and functional balance using star excursion test and single leg balance test
To assess physical performance, this study utilizes three specialized tools to measure strength, endurance, and balance. The isokinetic dynamometer serves as the clinical "gold standard" for quantifying muscle performance, providing highly standardized and sensitive data to induce abdominal muscle fatigue and evaluate the strength and endurance of the hip musculature. For balance assessment, the study uses the Star Excursion Balance Test (SEBT) to measure dynamic postural control; by recording the maximum distance a participant can reach while standing on one leg, it identifies sensorimotor deficits and provides a reliable index of stability. Complementing this is the Single Leg Stance (SLS) test, a validated, straightforward method for evaluating static balance by measuring the duration a participant can maintain a barefoot, one-legged position. Together, these tools provide a comprehensive evaluation of both strength-based fatigue and multi-directional stability.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Hip Abductors Muscle Strength
Periodo de tiempo: One week
Assess hip Abductor muscle strength using Isokinetic Dynamometer after fatiguing the abdominal muscles Unite: N.m
One week
Hip Extensor Muscle Strength
Periodo de tiempo: One week
Assess hip Extensor muscle strength using Isokinetic Dynamometer after fatiguing the abdominal muscles Unite: N.m
One week
Hip Flexor Muscle Strength
Periodo de tiempo: One Week
Assess hip Abductor muscle strength using Isokinetic Dynamometer after fatiguing the abdominal muscles Unite: N.m
One Week
Hip Adductor Muscle Strength
Periodo de tiempo: One Week
Assess hip Abductor muscle strength using Isokinetic Dynamometer after fatiguing the abdominal muscles Unite: N.m
One Week

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Hip Abductor Endurance Test
Periodo de tiempo: One Week
Assess hip Abductor muscle endurance using Isokinetic Dynamometer after fatiguing the abdominal muscles Measured by Fatigue Index
One Week
Hip Extensor Endurance Testing
Periodo de tiempo: One Week
Assess hip Extensor muscle endurance using Isokinetic Dynamometer after fatiguing the abdominal muscles Measured by Fatigue Index
One Week
Hip Flexor Endurance Testing
Periodo de tiempo: One Week
Assess hip Flexor muscle endurance using Isokinetic Dynamometer after fatiguing the abdominal muscles Measured by Fatigue Index
One Week
Hip Adductor Endurance Testing
Periodo de tiempo: One Week
Assess hip Adductor muscle endurance using Isokinetic Dynamometer after fatiguing the abdominal muscles Measured by Fatigue Index
One Week
Balance Testing Using Star Excursion test
Periodo de tiempo: One week
Balance testing after abdominal muscle fatigue using star excursion test Unite: Seconds
One week
Balance Testing Using Single Leg Stance Test
Periodo de tiempo: One Week
Balance testing after abdominal muscle fatigue using Single Leg Stance Test Unite: Seconds
One Week

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 (Estimado)

1 de mayo de 2026

Finalización primaria (Estimado)

31 de diciembre de 2026

Finalización del estudio (Estimado)

30 de enero de 2027

Fechas de registro del estudio

Enviado por primera vez

26 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

5 de mayo de 2026

Publicado por primera vez (Actual)

8 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

8 de mayo de 2026

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

5 de mayo de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • P.T.REC/012/006299

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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