Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

Virtual Reality Versus Traditional Exercise on EMG Activity in Postural Malalignment (EMG)

27 de septiembre de 2026 actualizado por: Mohamed Abdelmegeed, Hofstra University

Influence of Virtual Reality Versus Traditional Exercise on Trapezius Muscle EMG Activity in Relaxed and Corrected Postures Among Individuals With and Without Postural Malalignment

This study aims to investigate the immediate effects of virtual reality (VR)-based exercise compared with traditional Active free exercise on trapezius muscle activation in adults with and without postural malalignment. Surface electromyography (EMG) will be used to assess upper, middle, and lower trapezius muscle activity during relaxed and corrected postures and during VR and traditional exercise. Demographic data will be collected. The study will also assess posture, trapezius muscle strength, cervical range of motion, Activity level, craniovertebral angle, and neck proprioception. Approximately 40 adults aged 18-35 years will participate in a single study session. The findings may help determine whether VR-based rehabilitation provides an effective and engaging approach for assessing and training postural control and trapezius muscle activation.

Descripción general del estudio

Descripción detallada

This study will investigate the immediate effects of virtual reality (VR)-based exercise compared with traditional exercise on trapezius muscle activation in adults with and without postural malalignment. The study will include approximately 40 adults aged 18-35 years. Participants will be classified according to the presence or absence of postural abnormalities and symptoms.

At baseline, demographic and clinical information will be collected, followed by assessment of forward head posture, rounded shoulder posture, trapezius muscle strength, cervical range of motion, Activity level, craniovertebral angle and joint position sense. Forward head posture will be assessed using the craniovertebral angle obtained through digital photogrammetry, while rounded shoulder posture will be evaluated using the acromion-to-table distance. Symptomatic participants will additionally complete the Numeric Pain Rating Scale (NPRS) and Neck Disability Index (NDI).

Surface electromyography (sEMG) will be used to record the activity of the upper, middle, and lower trapezius muscles. EMG activity will be assessed during relaxed and corrected standing postures and continuously during the exercise conditions. EMG data will be normalized to maximum voluntary isometric contraction (MVIC) and expressed as a percentage of MVIC.

Each participant will complete both the VR-based intervention and the traditional TheraBand exercise intervention during a single study session. The VR intervention will be performed using a Virtualis rehabilitation system with an HTC Vive headset and motion controllers and will involve controlled upper-extremity movements designed to promote appropriate scapular and postural control. The traditional exercise condition will include standing active free exercises targeting the upper, middle, and lower trapezius muscles. A rest period will be provided between the two exercise conditions to minimize the potential effects of fatigue.

The primary comparison will examine normalized trapezius muscle activation during the VR-based and active free exercise conditions. Additional assessments will examine posture, trapezius muscle strength, cervical range of motion, and cervical proprioception. The study is intended to provide information regarding the immediate neuromuscular responses to VR-based rehabilitation and its potential application as an interactive approach to postural rehabilitation.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

40

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: Dina Alhamaky, Ph.D. in Physical Therapy
  • Número de teléfono: +971503963450
  • Correo electrónico: dinaali2008@cu.edu.eg

Ubicaciones de estudio

    • New York
      • Hempstead, New York, Estados Unidos, 11549
        • Hofstra University

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

18 años a 35 años (Adulto)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

participants will include healthy individuals or individuals with postural malalignment.

  • Age 18-35 years
  • Able to provide written informed consent
  • Able to stand and perform light movement tasks safely
  • Normal or corrected-to-normal vision
  • Sufficient intellectual ability to understand and follow instructions
  • Basic English proficiency to understand study instructions and questionnaires
  • For symptomatic participants, presence of postural dysfunction at baseline, including one or more of the following:
  • Forward head posture
  • Rounded shoulder posture

Exclusion Criteria:

  • - Epilepsy
  • Severe balance disorders
  • Major neurological or musculoskeletal conditions
  • Recent injuries
  • Use of medications affecting balance
  • Pregnancy

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: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: VR and Traditional Exercise

Participants will complete both a virtual reality (VR)-based exercise intervention and a traditional exercise intervention during a single study session. Trapezius muscle activity will be recorded using surface electromyography (sEMG) during both exercise conditions, with a rest period provided between interventions to minimize fatigue.

Participants will perform a Virtualis virtual reality rehabilitation activity using an HTC Vive headset and motion controllers while standing. The activity involves controlled upper-extremity reaching movements designed to encourage scapular retraction and depression and maintenance of an upright head and trunk posture. Trapezius muscle activity will be recorded continuously using surface electromyography (sEMG)

Participants will perform standing Active free exercises targeting the upper, middle, and lower trapezius muscles. Exercises will include diagonal arm elevation, horizontal abduction, and shoulder elevation. The duration of exercise during the active free condition will be matched to the duration of the VR intervention. Trapezius muscle activity will be recorded continuously using surface electromyography (sEMG).

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Trapezius Muscle Activation (sEMG)
Periodo de tiempo: During the single study session (approximately 35-45 minutes)

Surface electromyography (sEMG) will be used to measure upper, middle, and lower trapezius muscle activation during the virtual reality and Active free exercise conditions. EMG activity will be normalized to maximum voluntary isometric contraction (MVIC) and expressed as %MVIC.

During the single study session (approximately 35-45 minutes)

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Investigador principal: Mohamed Abdelmegeed, Ph.D. in Physical Therapy, Hofstra 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 (Estimado)

25 de octubre de 2026

Finalización primaria (Estimado)

25 de agosto de 2027

Finalización del estudio (Estimado)

25 de octubre de 2027

Fechas de registro del estudio

Enviado por primera vez

27 de septiembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

27 de septiembre de 2026

Publicado por primera vez (Actual)

2 de octubre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

2 de octubre de 2026

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

27 de septiembre de 2026

Última verificación

1 de septiembre 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. .

Suscribir