- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07711379
Immediate Effects of Ankle Joint Mobilization on Jump Performance in Healthy University Students
Immediate Effects of Ankle Joint Mobilization on Countermovement Jump Performance and Dorsiflexion Range of Motion in Healthy University Students
Descripción general del estudio
Estado
Intervención / Tratamiento
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
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Burhan Taşkaya, PhD
- Número de teléfono: 2449 +904364364949
- Correo electrónico: b.taskaya@alparslan.edu.tr
Ubicaciones de estudio
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Muş
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Muş, Muş, Turquía (Türkiye), 49250
- Muş Alparslan University, Vocational School of Health Services
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Contacto:
- Burhan Taşkaya, PhD
- Número de teléfono: +905052350030
- Correo electrónico: b.taskaya@alparslan.edu.tr
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Investigador principal:
- Burhan Taşkaya, PhD
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Sub-Investigador:
- Cengiz Taşkaya, PhD
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
Acepta Voluntarios Saludables
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
¿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 |
|---|---|
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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.
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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.
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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.
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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.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Countermovement Jump Performance
Periodo de tiempo: Immediately before the intervention and immediately after the intervention (single session).
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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.
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Immediately before the intervention and immediately after the intervention (single session).
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Ankle Dorsiflexion Range of Motion
Periodo de tiempo: Immediately before the intervention and immediately after the intervention (single session)
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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.
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Immediately before the intervention and immediately after the intervention (single session)
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Burhan Taşkaya, Muş Alparslan University
Publicaciones y enlaces útiles
Publicaciones Generales
- Vicenzino B, Branjerdporn M, Teys P, Jordan K. Initial changes in posterior talar glide and dorsiflexion of the ankle after mobilization with movement in individuals with recurrent ankle sprain. J Orthop Sports Phys Ther. 2006 Jul;36(7):464-71. doi: 10.2519/jospt.2006.2265.
- Blatter J, Brehm JM, Sordillo J, Forno E, Boutaoui N, Acosta-Perez E, Alvarez M, Colon-Semidey A, Weiss ST, Litonjua AA, Canino G, Celedon JC. Folate Deficiency, Atopy, and Severe Asthma Exacerbations in Puerto Rican Children. Ann Am Thorac Soc. 2016 Feb;13(2):223-30. doi: 10.1513/AnnalsATS.201508-549OC.
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 12.05.2026-247343
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
Información sobre medicamentos y dispositivos, documentos del estudio
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Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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