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Correlation Between Toilet Sitting Position, Ankle Range of Motion, and Lower Limb Strength in Children

4 de mayo de 2026 actualizado por: Riphah International University

Correlation Of Different Toilet Sitting On Ankle Range Of Motion, Constipation And Lower Limb Strength In School Going Children

This study investigates the relationship between different toilet sitting styles (squat vs. western) and their effects on ankle range of motion (ROM), constipation symptoms, and lower limb strength in school-going children aged 6-12 years. With increasing urbanization, the shift from traditional squat toilets to sitting toilets may influence children's musculoskeletal development and bowel health. Squatting involves greater ankle dorsiflexion and muscle activation, which may contribute to better lower limb strength and improved bowel function compared to sitting postures.

A comparative cross-sectional design will be used, including participants from public and private schools. Data on toilet usage habits will be collected along with demographic information. Ankle ROM will be measured using a goniometer, lower limb strength will be assessed through the 1-minute sit-to-stand test and standing long jump, and constipation symptoms will be evaluated using the PAC-SYM questionnaire. Data analysis will be conducted using SPSS version 26. Ethical approval will be obtained from the Research Ethics Committee of Riphah International University, Lahore.

Descripción general del estudio

Estado

Reclutamiento

Condiciones

Descripción detallada

This study aims to explore the correlation between different toilet sitting styles and their effects on ankle range of motion (ROM), constipation symptoms, and lower limb strength in school going children. With modernization and urbanization, there has been a significant shift from traditional squat toilets to western-style sitting toilets, especially in schools and households.This change in toileting posture may have a direct impact on musculoskeletal development and gastrointestinal health in growing children. Prolonged use of sitting toilets might limit the natural ankle dorsiflexion used during squatting and reduce muscle activation in the lower limbs, potentially contributing to strength limitations and altered bowel habits. The study intends to investigate whether habitual use of squat toilets promotes better ankle flexibility, stronger lower limbs, and fewer constipation-related symptoms in comparison to sitting toilet users.

A comparative cross-sectional study design will be employed, targeting children aged 6 to 12 years from selected public and private schools. After obtaining informed consent from guardians and assent from children, demographic data will be collected along with their toilet usage history. Ankle ROM will be measured using a goniometer, while lower limb strengthwill be assessed using the 1 minute sit-to-stand test and estimated long standing jump testing.Constipation symptoms will be evaluated using the Patient Assessment of Constipation Symptoms (PAC-SYM) questionnaire. Data will be analyzed through SPSS version26.0.Descriptive statistics will be used to determine the association between toilet type and the selected outcome variables. The synopsis will be presented to the Research Ethical committee of Riphah International University, Lahore, for ethical approval to conduct this study.

Tipo de estudio

De observación

Inscripción (Estimado)

191

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

  • Nombre: Muhammad Asif Javed, MS-PT
  • Número de teléfono: 923224209422
  • Correo electrónico: a.javed@riphah.edu.pk

Ubicaciones de estudio

    • Punjab Province
      • Lahore, Punjab Province, Pakistán, 54000
        • Reclutamiento
        • City District High School Lahore
        • Contacto:
        • Contacto:
          • Muhammad Asif Javed, MS-PT
          • Número de teléfono: 923224209422
          • Correo electrónico: a.javed@riphah.edu.pk

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

Acepta Voluntarios Saludables

No

Método de muestreo

Muestra no probabilística

Población de estudio

The study population will consist of school-going children aged 6 to 12 years enrolled in selected public schools. Both boys and girls will be included. Participants will be grouped based on their habitual toilet usage (squat toilet users and western-style sitting toilet users).Only children who are healthy, ambulatory, and able to perform physical tests will be included. Children with neurological conditions, musculoskeletal deformities, recent lower limb injuries, congenital abnormalities, or known gastrointestinal disorders (other than functional constipation) will be excluded.

Informed consent will be obtained from parents or guardians, along with assent from the children before participation.

Descripción

Inclusion Criteria:

  • Students age group: 6-12 year.
  • Both male and female groups
  • Normal developing children
  • Children who have been using either sitting or squatting toilet type .
  • Children's who are willing to participate and perform functional tasks.

Exclusion Criteria:

Children with abdominal surgery

  • Children with lower limb surgery
  • Children with acute or chronic disease like irritable bowel syndrome
  • Children using both toilet postures
  • Children with neurological or developmental delays affecting toilet independence like Cerebral Palsy and autism.
  • Children on medications that affect bowel movement (e.g., laxatives, opioid)

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

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Goniometer
Periodo de tiempo: Baeline
A goniometer is a reliable tool used to measure ankle range of motion (ROM), including dorsiflexion and plantarflexion. The axis is placed at the lateral malleolus, with arms aligned along the fibula and fifth metatarsal. Assessment is done in a seated or supine position** with the knee flexed or extended.
Baeline
1 Minute Sit-to-Stand Test
Periodo de tiempo: Baeline
1-minute Sit-to-Stand Test (1-MSTST) is a simple and reliable test to assess lower limb strength and endurance in children. The participant sits on a standard chair with arms crossed and performs maximum sit-to-stand repetitions in 60 seconds. Each full stand and return to sitting is counted as one repetition. The total number of repetitions is recorded, showing **high reliability in pediatric populations.
Baeline
Standing Long Jump
Periodo de tiempo: Baeline
The Standing Long Jump (SLJ), also known as the standing broad jump, is a field test used to evaluate explosive lower-limb power in children and adolescents. Participants start with both feet together just behind a marked line, execute a countermovement by flexing the knees and hips, swing their arms, and leap forward as far as possible, landing on both feet without falling backward. The distance from the take-off line to the back of the heel nearest the line is measured in centimeters. No shoes or minimal footwear are allowed to ensure consistency .Each participant performs two trials, and the longest valid jump is recorded as their score .Research including large pediatric samples confirms that the SLJ test exhibits excellent test-retest reliability.
Baeline
Patient Assessment of Constipation Symptoms (PAC-SYM) Questionnaire
Periodo de tiempo: Baeline
The PAC-SYM (Patient Assessment of Constipation Symptoms) is a validated questionnaire used to assess constipation severity over the past two weeks. It includes 12 items covering abdominal, stool, and rectal symptoms, rated on a 5-point Likert scale (0-4). Scores indicate severity ranging from minimal to very severe symptoms.
Baeline

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Ayisha Sana, MS-PT, Riphah International University

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)

13 de abril de 2026

Finalización primaria (Estimado)

10 de julio de 2026

Finalización del estudio (Estimado)

30 de agosto de 2026

Fechas de registro del estudio

Enviado por primera vez

4 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

4 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

4 de mayo de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • REC/RCR&AHS/AYISHASANA

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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