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Effects of Sustainable Exercise Habits in University Students (SUSTAIN-EX)

24 de junio de 2026 actualizado por: Yeditepe University

From Mind to Body: Evaluating the Effects of Sustainable Exercise Habits on Cognitive Awareness, Body Awareness, and Sleep Quality in University Students

This cross-sectional comparative study aims to evaluate the effects of sustainable exercise habits on cognitive awareness, body awareness, and sleep quality in university students.

The main hypotheses are:

H0: There is no difference in cognitive awareness, body awareness, and sleep quality between university students with sustainable exercise habits and those with a sedentary lifestyle.

H1: There is a difference in cognitive awareness, body awareness, and sleep quality between university students with sustainable exercise habits and those with a sedentary lifestyle.

Descripción general del estudio

Estado

Aún no reclutando

Intervención / Tratamiento

Descripción detallada

Healthy university students aged 18-25 who meet the inclusion criteria will be included in this comparative cross-sectional study to demonstrate the effects of sustainable exercise habits on cognitive awareness, body awareness, and sleep quality.

Participants will be divided into two different groups based on the International Physical Activity Questionnaire (IPAQ) results: the Sustainable Exercise Group and the Sedentary Group. The Sustainable Exercise Group will consist of students who have been performing at least 150 minutes of moderate-to-vigorous physical activity per week regularly for at least the last 6 months. The Sedentary Group will include individuals with a weekly physical activity duration of less than 60 minutes or those without a regular exercise habit for the last 6 months.

No intervention or experimental procedure will be applied to the participants. All assessments will be prepared as online questionnaires and sent to the participants via Google Forms.

Before the evaluation, participants will be informed about the study and their consent will be obtained online. Following this, the participants' sociodemographic characteristics, physical activity routines, and sedentary behaviors will be questioned with a structured evaluation form. The physical activity levels, body awareness, decision-making styles, critical thinking dispositions, and sleep quality of the participants will be evaluated using the International Physical Activity Questionnaire-Short Form, Body Awareness Questionnaire, Melbourne Decision Making Scale, Marmara Critical Thinking Dispositions Scale, and Pittsburgh Sleep Quality Index, respectively.

Tipo de estudio

De observación

Inscripción (Estimado)

140

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

Copia de seguridad de contactos de estudio

Ubicaciones de estudio

    • Istanbul
      • Istanbul, Istanbul, Turquía (Türkiye), 34755
        • Yeditepe University Faculty of Health 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

Método de muestreo

Muestra no probabilística

Población de estudio

This study will include healthy university students aged 18 to 25 who are currently studying at universities in Turkey. The study population is divided into two main groups based on their physical activity levels: a sustainable exercise group consisting of students who exercise regularly, and a sedentary group consisting of students who do not exercise regularly.

Descripción

Inclusion Criteria:

  • Being a university student aged between 18 and 25 years
  • Volunteering to participate in the study

Exclusion Criteria:

  • Having any diagnosed psychiatric disorder
  • Regularly using medications that affect sleep patterns or cognitive functions
  • Having been diagnosed with a sleep disorder
  • Having a history of substance or alcohol addiction
  • Having had an acute illness within the last 1 month
  • Having undergone surgery within the last 6 months

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
Sustainable Exercise Group
University students who have been performing at least 150 minutes of moderate-to-vigorous physical activity per week regularly for at least the last 6 months.
No pharmacological or physical intervention is applied. Participants are assigned to groups based on their self-reported physical activity habits. Assessment consists of an online survey battery to evaluate cognitive awareness, body awareness, and sleep quality.
Sedentary Group
University students with a weekly physical activity duration of less than 60 minutes or those without a regular exercise habit for the last 6 months.
No pharmacological or physical intervention is applied. Participants are assigned to groups based on their self-reported physical activity habits. Assessment consists of an online survey battery to evaluate cognitive awareness, body awareness, and sleep quality.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
International Physical Activity Questionnaire (IPAQ) - Short Form
Periodo de tiempo: 8-week period between April 2026 and May 2026
The IPAQ-Short Form will be used to determine the physical activity levels of the participants. This questionnaire consists of 7 questions and provides information about the duration of vigorous activity, moderate activity, walking, and sitting performed in the last 7 days. The data obtained will be calculated in MET-minutes/week. Based on the results, participants will be classified as physically inactive, having low activity level, or adequate activity level.
8-week period between April 2026 and May 2026

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Body Awareness Questionnaire
Periodo de tiempo: 8-week period between April 2026 and May 2026
This questionnaire will be used to measure individuals' awareness of their non-pathological bodily processes, such as sensitivity to bodily rhythms, abnormal changes, and variations in body functions. It consists of 18 items. A high total score indicates that the individual has a high level of body awareness.
8-week period between April 2026 and May 2026
Melbourne Decision Making Scale
Periodo de tiempo: 8-week period between April 2026 and May 2026
This scale will be used to evaluate participants' decision-making self-esteem and decision-making styles. The scale consists of two parts: the first part measures self-esteem in decision making, and the second part measures decision-making styles including careful, avoidant, procrastinating, and panic decision making. It includes a total of 22 items.
8-week period between April 2026 and May 2026
Marmara Critical Thinking Dispositions Scale
Periodo de tiempo: 8-week period between April 2026 and May 2026
This scale will be used to determine the critical thinking dispositions of the university students. It is a measurement tool consisting of 28 items that include sub-dimensions such as reasoning, searching, evidence gathering, and open-mindedness.
8-week period between April 2026 and May 2026
Pittsburgh Sleep Quality Index (PSQI)
Periodo de tiempo: 8-week period between April 2026 and May 2026
The PSQI will be used to evaluate the participants' sleep quality and sleep disturbance levels over the past month. The scale consists of 19 self-report questions evaluating 7 components: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication, and daytime dysfunction. A total score of 5 or higher is evaluated as poor sleep quality.
8-week period between April 2026 and May 2026

Colaboradores e Investigadores

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

Patrocinador

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

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)

10 de junio de 2026

Finalización primaria (Estimado)

27 de julio de 2026

Finalización del estudio (Estimado)

30 de julio de 2026

Fechas de registro del estudio

Enviado por primera vez

24 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

24 de junio de 2026

Publicado por primera vez (Actual)

30 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

30 de junio de 2026

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

24 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

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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