Artificial Intelligence-Based Postural Feedback for Scoliosis
22 de junio de 2026 actualizado por: Rommanee Rojasavastera, Mahidol University
The Effect of Artificial Intelligence-Based Postural Feedback on Posture Correction in Idiopathic Scoliosis Patients
Due to advancements in technology, Posture-Analyzing and Virtual Reconstructing (PAViR) systems were developed.
They used Red-Green-Blue-Depth camera sensors and artificial intelligence to evaluate human posture alignment, muscle balance, and movement without the use of radiation or physical markers.
This technology served as a portable, X-ray-like device that was safe and user-friendly, providing detailed views of bone and muscle models alongside easy-to-understand 3D visualizations.
However, how to utilize the data obtained from PAViR to support traditional treatment remained unclear.
To fill this gap, this study aimed to investigate the effects of AI-based postural feedback on posture correction in patients with idiopathic scoliosis.
Descripción general del estudio
Estado
Aún no reclutando
Intervención / Tratamiento
Tipo de estudio
Intervencionista
Inscripción (Estimado)
30
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
- Nombre: Rommanee Rojasavastera, M.Sc.
- Número de teléfono: +66837830777
- Correo electrónico: rommanee.roj@mahidol.ac.th
Ubicaciones de estudio
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Changwat Nakhon Pathom
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Salaya, Changwat Nakhon Pathom, Tailandia, 73170
- Faculty of Physical Therapy, Mahidol University
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Contacto:
- Rommanee Rojasavastera, M.Sc.
- Número de teléfono: +66837830777
- Correo electrónico: rommanee.roj@mahidol.ac.th
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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
- Adulto
Acepta Voluntarios Saludables
No
Descripción
Inclusion Criteria:
- Diagnosis of adolescent idiopathic scoliosis (AIS) by a physician.
- Aged between 10 and 18 years.
- Cobb angle between 10 and 40 degrees.
Exclusion Criteria:
- Leg length discrepancy greater than 2 cm, measured from the anterior superior iliac spine (ASIS) to the lateral malleolus.
- Previous history of spinal surgery.
- Musculoskeletal or neurological injuries that affect balance and gait.
- Inability to follow the research 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: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Experimental: AI-Based Postural Feedback Group
Participants in the experimental group received postural feedback via the PAViR system, integrated with posture correction exercises and physical therapy for scoliosis.
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The physical therapist reported the findings from the PAViR system to the participants during a 10-minute session.
Data regarding skeletal alignment and muscle imbalances were provided to enhance participants' self-awareness of their specific postural issues.
Furthermore, these insights were integrated into the subsequent training sessions for the experimental group.
The physical therapist conducted 60-minute sessions.
These sessions were grounded in the principles of the Schroth Method and Physiotherapeutic Scoliosis-Specific Exercises (PSSE).
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Comparador activo: Conventional Postural Feedback Group
Participants in the control group received the same exercise and therapy sessions, but without the postural feedback provided by the PAViR system.
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The physical therapist conducted 60-minute sessions.
These sessions were grounded in the principles of the Schroth Method and Physiotherapeutic Scoliosis-Specific Exercises (PSSE).
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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REEDCO postural score
Periodo de tiempo: before and immediately after intervention
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The REEDCO Posture Assessment was used to evaluate postural scores during comfortable standing and postural self-correction.
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before and immediately after intervention
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Angle of trunk rotation
Periodo de tiempo: before and immediately after intervention
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A scoliometer was used to evaluate the angle of trunk rotation during Adam's Forward Bend Test.
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before and immediately after intervention
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Postural Variables Derived from a 3D Motion Analysis System
Periodo de tiempo: before and immediately after intervention
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A 3D motion analysis system (VICON Motion Systems Ltd., Oxford, UK) was used to evaluate postural variables during comfortable standing, postural self-correction, and the Adam's Forward Bend Test.
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before and immediately after intervention
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Postural Variables Derived from a PAViR System
Periodo de tiempo: before and immediately after intervention
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A PAViR system (MGsolutions Inc., Seoul, South Korea) was used to evaluate postural variables during comfortable standing, postural self-correction, and the Adam's Forward Bend Test.
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before and immediately after intervention
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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Illness Perception
Periodo de tiempo: before and immediately after intervention
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The Brief Illness Perception Questionnaire (IPQ-B) was an accurate and valid assessment tool to measure and monitor illness perceptions.
It consisted of nine items rated on a scale from 0 (minimum) to 10 (maximum).
The first five assessed cognitive perceptions such as the effect on life (item 1); duration of illness (item 2); control over illness (item 3); beliefs about the effectiveness of treatment (item 4); and experience of symptoms (item 5).
Items 6 and 8 assessed emotional aspects, which included concern about the illness and a multifaceted question about mood.
Item 7 assessed the degree of understanding of the illness.
The final item was open-ended, asking respondents to rank the three most important factors causing their illness.
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before and immediately after intervention
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Exercise Motivation
Periodo de tiempo: before and immediately after intervention
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The Behavioral Regulation in Exercise Questionnaire-2 (BREQ-2) was a 19-item questionnaire that measured the stages of the self-determination continuum with respect to motivation to exercise using a 5-point Likert scale (0 = not true for me, 4 = very true for me) and was modified by Markland and Tobin.
The version by Markland and Tobin added an amotivation factor to the original external, introjected, identified, and intrinsic regulation factors.
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before and immediately after intervention
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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)
1 de julio de 2026
Finalización primaria (Estimado)
1 de julio de 2027
Finalización del estudio (Estimado)
1 de julio de 2027
Fechas de registro del estudio
Enviado por primera vez
17 de junio de 2026
Primero enviado que cumplió con los criterios de control de calidad
22 de junio de 2026
Publicado por primera vez (Actual)
25 de junio de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
25 de junio de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
22 de junio de 2026
Última verificación
1 de junio de 2026
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- MU-CIRB 2026/171.2603
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
SÍ
Descripción del plan IPD
Research data will be shared in a de-identified format only; for instance, participant names will be replaced with codes, and faces will be blurred in all images.
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. .