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Retro Walking With and Without Bosu Ball for Balance and Mobility in Hearing Impaired Children

5 de mayo de 2026 actualizado por: Riphah International University

Comparative Effects of Retro Walking With and Without Bosu Ball on Balance and Mobility in Children With Hearing Impairment

his randomized controlled trial aims to evaluate the effects of retro walking with and without BOSU ball training on balance and mobility in hearing-impaired children aged 8-12 years. A total of 24 participants will be divided into experimental and control groups. The experimental group will receive retro walking along with BOSU ball training, while the control group will perform retro walking only for 8 weeks. Balance and mobility will be assessed using the Pediatric Balance Scale, Timed Up and Go Test, and One-Leg Stance Test. Data will be collected from specialized schools in Lahore and analyzed using SPSS 27. Ethical approval will be obtained prior to study commencement.

Descripción general del estudio

Estado

Reclutamiento

Descripción detallada

Children with hearing impairment often experience balance and motor deficits due to concomitant damage to the vestibular structures. Interventions focusing on balance training have shown promise in improving postural control and motor coordination in this population. Retro walking, or backward walking, has been identified as an effective exercise to enhance balance and motor control. Additionally, the BOSU ball, a fitness training device that provides an unstable surface, is commonly used for balance training. However, the combined effect of retro walking and BOSU ball training on balance and mobility in hearing-impaired children remains underexplored. The aim of this study is to investigate the effects of retro walking on balance and mobility with and without Bosu ball in hearing impaired children.

The study design will be a randomized control trial. Data will be collected from Govt. Deaf and Defective Hearing Model High School for Girls Rajgarh and Deaf Reach School, Training Center and College, Lahore. The study will be completed in 10 months after the approval of synopsis. Children aged 8 to 12 years will be randomly assigned either into the experimental group(n=12) or control group (n=12). The experimental group will be provided retro walking exercises for 30 minutes 8 weeks and BOSU ball will also be 8 weeks duration. The Control group will provide only retro walking exercises for 8 weeks. Participants fulfilling the eligibility criteria will be asked to assign the consent form before entering into the study. Balance will be measured by pediatric balance scale, mobility will be measured by time up and go test and static balance will be measured by one leg stance test. The synopsis will be presented to Research Ethical Committee of Riphah International University, Lahore for ethical approval to conduct this study. Data will be analyzed through SPSS 27.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

24

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.

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
        • Govt. Deaf and Defective Hearing Model High School for girls, Rajgarh
        • 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

Descripción

Inclusion Criteria:

  • Age 8 to 12 years.
  • Children with hearing loss in right and left ear (bilateral).
  • Children with hearing-impaired intensity over 61 dB.
  • Both genders will be included.
  • Balance cut off value <45 on pediatrics balance scale.

Exclusion Criteria:

  • Presence of neurologic disease.
  • Hyperactivity and vision problems.
  • Have any musculoskeletal disorders.
  • Children with cochlear implant.
  • Children with leg length discrepancy

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: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Retro walking with bosu ball
The experimental group will receive a structured balance and mobility training program that includes retro walking performed with the use of a Bosu ball. Participants will practice backward walking or the unstable surface of the Bosu ball.
The BOSU ball intervention includes a series of balance and strength exercises performed in both stable (flat side up) and unstable (bouncy side up) positions. Activities involve weight shifting, circular foot movements, squats, single-leg stance, leg abduction, lunges, push-ups, and abdominal crunches to challenge stability. These movements are designed to improve balance, core strength, coordination, and functional mobility under controlled conditions.all these interventions for 8 weeks
Otros nombres:
  • Retro Walking
Comparador activo: Retro walking without bosu ball
The control group will participate in a conventional balance and mobility training program involving retro walking on a stable, flat surface without the use of a BOSU ball. Participants will perform backward walking only under supervision.
The intervention consists of structured retro walking exercises designed to improve balance, coordination, and mobility. It includes variations such as knee and heel pulling, slalom movements, cross steps, skipping, and fast backward running with different body and foot positions. These activities are performed under supervision to enhance postural control, dynamic stability, and functional walking performance

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Pediatrics Balance Scale
Periodo de tiempo: Baseline, 8weeks
The Pediatric Balance Scale (PBS) is a valid and reliable test used to assess functional balance in children. It includes 14 simple activity-based tasks scored out of 56, where higher scores indicate better balance. The test is quick to administer and commonly used in children with balance impairments, including hearing loss.
Baseline, 8weeks
Time Up and Go Test
Periodo de tiempo: Baseline, 8weeks
The Timed Up and Go Test (TUG) is a reliable and valid tool used to assess functional mobility and dynamic balance in children aged 3-18 years. It has strong test-retest, intra-rater, and inter-rater reliability and correlates well with other measures of balance, strength, and functional ability.
Baseline, 8weeks
Single leg stance test
Periodo de tiempo: Baseline, 8weeks
It is used to assess static balance by measuring how long a child can stand on one leg. The child maintains a specific posture while timing starts when one foot is lifted and stops when balance is lost or the foot touches the ground. Proper posture is required throughout, and the test is repeated if incorrect positioning occurs.
Baseline, 8weeks

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Salma Kanwal, MS-PT, Riphah International University

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.

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)

15 de abril de 2026

Finalización primaria (Estimado)

5 de julio de 2026

Finalización del estudio (Estimado)

5 de agosto de 2026

Fechas de registro del estudio

Enviado por primera vez

5 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

5 de mayo de 2026

Publicado por primera vez (Actual)

11 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

11 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

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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