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Exercise Snacks and Muscular Fitness in Sedentary Young Women (ES)

2 de julio de 2026 actualizado por: Ziren Zhao, Chongqing Normal University

Effects of a 75-Minute Weekly Exercise Snack on Muscular Fitness in Sedentary Young Women

This randomized controlled study examined whether exercise snacks could improve skeletal muscle strength and related physical fitness in sedentary female university students. Eligible participants were sedentary women aged 18 to 25 years who were randomly assigned to an exercise snacks group, a regular exercise group, or a control group. The intervention lasted 8 weeks. The exercise snacks group accumulated short bouts of exercise across the day, while the regular exercise group completed more concentrated exercise sessions three times per week. The control group maintained their usual lifestyle. Muscle strength and related physical fitness were assessed before and after the intervention. The study aimed to evaluate the effectiveness, feasibility, and safety of exercise snacks in a university setting.

Descripción general del estudio

Descripción detallada

Sedentary behavior is common among university students and may contribute to reduced physical fitness and lower skeletal muscle function. Exercise snacks are short bouts of physical activity performed repeatedly throughout the day and may offer a time-efficient strategy for interrupting prolonged sitting.

This single-center randomized controlled study was conducted at Chongqing Normal University. Sedentary female university students aged 18 to 25 years were screened for eligibility. Participants completed baseline assessments and were randomly allocated to an exercise snacks group, a regular exercise group, or a control group.

The intervention lasted 8 weeks. The exercise snacks group performed short exercise bouts distributed throughout the day, with a total weekly exercise volume of approximately 75 minutes. The regular exercise group performed exercise three times per week, with each session lasting approximately 25 minutes. Both intervention groups received exercise guidance, reminders, adherence monitoring, and ratings of perceived exertion through the Tizhiyun mobile application. The control group maintained their usual study and lifestyle routines without additional study-prescribed exercise.

Primary outcomes included isokinetic muscle strength, surface electromyography, and mid-thigh isometric pull performance. Secondary outcomes included standing long jump, knee push-ups, and bodyweight squats to exhaustion. Outcome assessments were conducted at baseline and after the 8-week intervention. Adherence, perceived exertion, and exercise-related adverse events were recorded during the study period.

Tipo de estudio

Intervencionista

Inscripción (Actual)

90

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

    • Chongqing Municipality
      • Chongqing, Chongqing Municipality, Porcelana, 401331
        • Chongqing Normal University

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:

  • Female university students aged 18 to 25 years.
  • Daily sedentary time of at least 8 hours, assessed using a sedentary behavior questionnaire.
  • No contraindications to exercise based on the Physical Activity Readiness Questionnaire.
  • No regular exercise participation during the previous 3 months.

Exclusion Criteria:

  • Clinical conditions that make participation in exercise inappropriate.
  • Substantial body weight fluctuation during the previous 3 months.
  • Hypertension, cardiovascular or cerebrovascular disease, or use of related medications.

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: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Exercise Snacks Group
Participants received the exercise snacks intervention for 8 weeks. Exercise was accumulated through short bouts distributed across the day, with a total weekly exercise volume of approximately 75 minutes. Participants completed approximately 11 minutes of exercise on weekdays and 10 minutes on weekends. Exercise guidance, reminders, adherence monitoring, and ratings of perceived exertion were provided through the Tizhiyun mobile application.
Participants performed an 8-week exercise snacks program consisting of short bouts of physical activity distributed across the day. The program was performed 7 days per week, with approximately 75 minutes of exercise per week. Participants completed approximately 11 minutes of short exercise on weekdays and 10 minutes on weekends. Exercise guidance, reminders, adherence monitoring, and ratings of perceived exertion were provided through the Tizhiyun mobile application.
Comparador activo: Regular Exercise Group
Participants received a regular exercise intervention for 8 weeks. Exercise was completed three times per week, with each session lasting approximately 25 minutes.
Participants performed an 8-week regular exercise program. Exercise sessions were completed three times per week on Monday, Wednesday, and Friday, with each session lasting approximately 25 minutes. Exercise guidance, reminders, adherence monitoring, and ratings of perceived exertion were provided through the Tizhiyun mobile application.
Sin intervención: Usual Lifestyle Control Group
Participants maintained their usual study and lifestyle routines during the 8-week study period and did not receive additional study-prescribed exercise.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Isokinetic Muscle Strength
Periodo de tiempo: Baseline and Week 8
Isokinetic muscle strength was assessed using an isokinetic dynamometer during standardized testing. Change from baseline to post-intervention was evaluated.
Baseline and Week 8
Surface Electromyography Activity
Periodo de tiempo: Baseline and Week 8
Surface electromyographic activity was recorded during standardized muscle strength testing to evaluate neuromuscular activation.
Baseline and Week 8
Mid-Thigh Isometric Pull
Periodo de tiempo: Baseline and Week 8
Maximal force generated during a standardized mid-thigh isometric pull test was assessed to evaluate whole-body isometric strength.
Baseline and Week 8

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Standing Long Jump
Periodo de tiempo: Baseline and Week 8
Standing long jump distance was assessed using a standardized test of lower-body explosive performance.
Baseline and Week 8
Knee Push-Ups
Periodo de tiempo: Baseline and Week 8
The number of correctly completed knee push-up repetitions was assessed using a standardized muscular endurance test.
Baseline and Week 8
Bodyweight Squats to Exhaustion
Periodo de tiempo: Baseline and Week 8
The number of correctly completed bodyweight squats performed to volitional exhaustion was assessed as an indicator of lower-body muscular endurance.
Baseline and Week 8

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)

20 de abril de 2026

Finalización primaria (Actual)

25 de junio de 2026

Finalización del estudio (Actual)

25 de junio de 2026

Fechas de registro del estudio

Enviado por primera vez

2 de julio de 2026

Primero enviado que cumplió con los criterios de control de calidad

2 de julio de 2026

Publicado por primera vez (Actual)

9 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

9 de julio de 2026

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

2 de julio de 2026

Última verificación

1 de julio de 2026

Más información

Términos relacionados con este estudio

Términos MeSH relevantes adicionales

Otros números de identificación del estudio

  • CSK2026051

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

De-identified individual participant data will not be shared outside the research team because the current informed consent and data management plans limit the use of participant data to this study and do not include external data sharing.

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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