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Immediate Effects of Ankle Joint Mobilization on Jump Performance in Healthy University Students

14 de julio de 2026 actualizado por: Burhan Taşkaya, Muş Alparslan University

Immediate Effects of Ankle Joint Mobilization on Countermovement Jump Performance and Dorsiflexion Range of Motion in Healthy University Students

The purpose of this randomized controlled study is to investigate the immediate effects of ankle joint mobilization on countermovement jump performance and ankle dorsiflexion range of motion in healthy university students. Participants will be randomly assigned to either an ankle joint mobilization group or a sham mobilization group. Countermovement jump performance will be assessed using the My Jump Lab mobile application, and ankle dorsiflexion range of motion will be measured using the weight-bearing lunge test with a digital inclinometer before and immediately after the intervention. The findings of this study are expected to improve the understanding of the acute effects of ankle joint mobilization on functional performance and ankle mobility.

Descripción general del estudio

Descripción detallada

Vertical jump performance is an important indicator of lower-extremity explosive power and neuromuscular function. Adequate ankle dorsiflexion range of motion plays a critical role in force production, movement efficiency, and landing mechanics during jumping tasks. Previous studies have demonstrated that ankle joint mobilization can improve dorsiflexion range of motion through mechanical and neurophysiological mechanisms. However, limited evidence exists regarding whether these immediate improvements in ankle mobility translate into enhanced jump performance in healthy individuals.

This randomized controlled study aims to evaluate the immediate effects of ankle joint mobilization on countermovement jump performance and ankle dorsiflexion range of motion in healthy university students.

Approximately 50 healthy university students will be recruited and randomly allocated to either an ankle joint mobilization group or a sham mobilization group (25 participants per group). Before the intervention, all participants will undergo assessments of countermovement jump performance using the My Jump Lab mobile application and ankle dorsiflexion range of motion using the weight-bearing lunge test with a digital inclinometer.

Participants in the intervention group will receive ankle joint mobilization using the Mobilization with Movement (MWM) technique. Participants in the sham group will be positioned similarly and perform the same movement without the application of therapeutic posterior talar glide. Immediately after the intervention, all outcome measures will be repeated using the same standardized procedures.

The primary outcome will be countermovement jump performance, while the secondary outcome will be ankle dorsiflexion range of motion. The results of this study may provide evidence regarding the immediate effects of ankle joint mobilization on functional performance and may contribute to the development of evidence-based manual therapy interventions for improving lower-extremity performance

Tipo de estudio

Intervencionista

Inscripción (Estimado)

52

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

Ubicaciones de estudio

    • Muş
      • Muş, Muş, Turquía (Türkiye), 49250
        • Muş Alparslan University, Vocational School of Health Services
        • Contacto:
        • Investigador principal:
          • Burhan Taşkaya, PhD
        • Sub-Investigador:
          • Cengiz Taşkaya, PhD

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:

  • Healthy university students aged 18-30 years.
  • Willing to participate and provide written informed consent.
  • No history of lower extremity musculoskeletal injury or surgery within the -previous 6 months.
  • No neurological or vestibular disorders affecting balance or movement.
  • No contraindications to manual therapy.

Exclusion Criteria:

  • Current pain in the lower extremity or spine.
  • History of ankle fracture or surgery.
  • Acute lower extremity injury within the previous 6 months.
  • Any systemic, neurological, or rheumatological disease affecting movement.
  • Participation in another intervention study during the study period.
  • Inability to complete the assessment procedures.

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: Ciencia básica
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Mobilization with Movement (MWM)
Participants assigned to this group will receive ankle joint mobilization using the Mobilization with Movement (MWM) technique. A sustained posterior talar glide will be applied while participants actively perform a weight-bearing lunge movement. The intervention will consist of three sets of ten repetitions, with a 2-3 second hold at the end range of each repetition.
A Mulligan Mobilization with Movement technique will be applied to the talocrural joint. During active weight-bearing lunge movement, a sustained posterior talar glide will be applied by the therapist. The intervention will consist of three sets of ten repetitions.
Comparador falso: Sham Mobilization
Participants assigned to this group will undergo the same positioning and active weight-bearing lunge movement as the experimental group. However, no therapeutic posterior talar glide will be applied. This procedure is designed to mimic the intervention without providing a therapeutic mobilization effect.
Participants will perform the same active movement in the same position as the experimental group. The therapist will maintain hand contact without applying a therapeutic posterior talar glide.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Countermovement Jump Performance
Periodo de tiempo: Immediately before the intervention and immediately after the intervention (single session).
Countermovement jump (CMJ) performance will be assessed using the My Jump Lab mobile application. Participants will perform three maximal countermovement jumps with their hands on their hips, and the highest jump height (cm) will be recorded.
Immediately before the intervention and immediately after the intervention (single session).

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Ankle Dorsiflexion Range of Motion
Periodo de tiempo: Immediately before the intervention and immediately after the intervention (single session)
Ankle dorsiflexion range of motion will be measured using the weight-bearing lunge test with a digital inclinometer. Three measurements will be obtained, and the average value (degrees) will be used for analysis.
Immediately before the intervention and immediately after the intervention (single session)

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Burhan Taşkaya, Muş Alparslan 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 (Estimado)

25 de julio de 2026

Finalización primaria (Estimado)

15 de agosto de 2026

Finalización del estudio (Estimado)

15 de agosto de 2026

Fechas de registro del estudio

Enviado por primera vez

14 de julio de 2026

Primero enviado que cumplió con los criterios de control de calidad

14 de julio de 2026

Publicado por primera vez (Actual)

17 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

17 de julio de 2026

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

14 de julio de 2026

Última verificación

1 de julio de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

Individual participant data will not be shared because the study involves a limited number of participants and no consent for public sharing of anonymized individual-level data was obtained. Aggregate study results will be reported in scientific publications.

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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