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Impact of Forward Head Posture on Postural Stability and Gait Kinematics

17 de mayo de 2026 actualizado por: Yasmin Magdy Othman, Cairo University

Impact of Forward Head Posture on Postural Stability and Kinematic Gait Characteristics: A Comparative Cross Sectional Study

  1. Evaluate postural stability in subjects with forward head posture versus matching controls.
  2. Evaluate gait parameters in subjects with forward head posture versus matching controls.
  3. Investigate the correlation between postural stability and kinematic gait parameters in each group.

Descripción general del estudio

Descripción detallada

Forward head posture (FHP) is a common sagittal-plane postural deviation characterized by anterior translation of the head relative to the trunk. It has become increasingly prevalent among young adults due to prolonged use of computers, smartphones, and other digital devices. FHP has been associated with musculoskeletal dysfunction, altered cervical biomechanics, impaired proprioception, and deficits in postural control.

Recent evidence indicates that altered cervical alignment may influence not only local cervical function but also whole-body balance control and locomotor performance. Changes in head and neck alignment may disrupt vestibular, visual, and somatosensory integration, thereby affecting postural stability and gait efficiency. Although previous studies have independently investigated the effects of FHP on balance or gait, the relationship between postural stability and detailed kinematic gait characteristics in individuals with FHP remains insufficiently understood.

Therefore, this comparative cross-sectional study will investigate the impact of forward head posture on postural stability and kinematic gait characteristics in asymptomatic young adults.

A total of 66 participants of both sexes, aged between 18 and 35 years, will be recruited and assigned into two groups:

Forward Head Posture Group: participants with craniovertebral angle less than 50 degrees.

Control Group: participants with normal cervical posture.

Each participant will attend one laboratory-based assessment session.

Assessment Procedures

  1. Postural Assessment

    Craniovertebral angle will be measured using standardized lateral photography and a smartphone-based digital angle measurement application for group allocation.

  2. Postural Stability Assessment

    Dynamic postural stability will be assessed using the Biodex Balance System. Participants will perform bilateral stance testing at stability level 6 for three trials of 20 seconds each, with 10-second rest intervals. Outcome measures will include:

    Overall Stability Index Anterior-Posterior Stability Index Mediolateral Stability Index

  3. Gait Assessment

Spatiotemporal gait characteristics will be assessed using the Biodex Gait Trainer. Following a familiarization period, participants will walk under two testing conditions:

Self-selected comfortable walking speed Fast walking speed

Outcome measures will include:

Walking velocity Step length Cadence Symmetry indices Temporal gait parameters Primary Objective

To compare postural stability and gait characteristics between young adults with forward head posture and healthy controls.

Secondary Objective

To investigate the relationship between postural stability measures and gait parameters within each group.

Statistical Analysis

Descriptive statistics will be calculated for all variables. Between-group comparisons will be performed using one-way multivariate analysis of variance (MANOVA). Correlation analysis will be performed to examine associations between postural stability and gait parameters. Statistical significance will be set at p < 0.05.

Tipo de estudio

De observación

Inscripción (Estimado)

66

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

  • Nombre: Yasmin Magdy Othman Yasmin Magdy Othman, Bachelor
  • Número de teléfono: 01061051254
  • Correo electrónico: ymothman@msa.edu.eg

Ubicaciones de estudio

      • Giza, Egipto
        • Reclutamiento
        • Cairo University
        • Contacto:
          • Cairo university Cairo University
          • Número de teléfono: 0237617691
          • Correo electrónico: eth.com@pt.cu.edu

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

The study population will consist of adult males and females recruited from the university community and surrounding local community. Participants aged 18-35 years will be screened for eligibility. Eligible participants will be allocated into two cohorts based on head posture assessment using craniovertebral angle measurement: individuals with forward head posture and healthy individuals with normal head posture. Participants must be able to walk independently without assistive devices and have no history of neurological, musculoskeletal, vestibular, or visual disorders that may affect balance or gait performance.

Descripción

Inclusion Criteria:

  • Cranio-vertebral angle less than 50◦
  • Age from 18-35 years old (Young adults)
  • BMI from 18.5-24.9
  • Participants can walk independently without assistive devices

Exclusion Criteria:

  • Individuals are excluded if they have had:

    • Neck trauma, recent fractures, or Surgery or any underlying neurological or systemic conditions affecting the neck
    • Pregnancy or Malignancy
    • any inability to comprehend or respond to study assessments
    • Any known respiratory or cardiovascular conditions that might affect the results of gait analysis
    • Vestibular problems, visual problems, and sensory impairment affecting balance
    • If they are undergoing current physical therapy or ergonomic intervention for FHP

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
Forward Head Posture Group
Participants with clinically identified forward head posture based on craniovertebral angle assessment. Postural stability and gait kinematic characteristics will be assessed during standardized testing procedures.
Control Group
Age- and sex-matched healthy participants with normal head posture. Postural stability and gait kinematic characteristics will be assessed using the same standardized procedures.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Walking speed
Periodo de tiempo: through study completion, an average of 1 year
Kinematic Gait characteristic, measured in meter/second
through study completion, an average of 1 year
Overall stability index
Periodo de tiempo: through study completion, an average of 1 year
one of the postural stability outcome measures, Higher values indicate poorer balance
through study completion, an average of 1 year
Step Cycle
Periodo de tiempo: through study completion, an average of 1 year
Kinematic Gait characteristic measured in cycle/sec
through study completion, an average of 1 year
Mediolateral Stability index
Periodo de tiempo: through study completion, an average of 1 year
one of the postural stability index outcome measures, Higher values indicate poorer balance
through study completion, an average of 1 year
Anteroposterior Stability index
Periodo de tiempo: through study completion, an average of 1 year
one of the postural stability outcome measures, Higher values indicate poorer balance in the anteroposterior directions
through study completion, an average of 1 year
Step Length
Periodo de tiempo: through study completion, an average of 1 year
Kinematic gait characteristic, measured in cm
through study completion, an average of 1 year

Colaboradores e Investigadores

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

Patrocinador

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)

11 de mayo de 2026

Finalización primaria (Estimado)

11 de mayo de 2026

Finalización del estudio (Estimado)

30 de diciembre de 2026

Fechas de registro del estudio

Enviado por primera vez

11 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

17 de mayo de 2026

Publicado por primera vez (Actual)

22 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

22 de mayo de 2026

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

17 de mayo de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • P.T.REC/012/006413

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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