Comparing Conventional Abdominal Ultrasound Scanning Versus a Robotic Assisted Ultrasonography System (ROBUST)
Comparing Conventional Abdominal Ultrasound Scanning Versus a Robotic Assisted Ultrasonography System (ROBUST): a Pilot Study
Work-related musculoskeletal disorders (WRMSD) among sonographers/radiographers are prevalent in the healthcare industry. This pilot study will evaluate the use of a robotic assisted ultrasonography system (ROBUST) against the conventional abdominal ultrasound scanning procedure. The ROBUST will be developed to provide 6 degrees of freedom to allow radiographers to perform abdominal scanning without having to reach over patients.
10 sonographers with at least 5 years of experience will be recruited from SGH and SKH, to perform abdominal ultrasound scans on healthy volunteers. Each sonographer will be randomly assigned to scan a volunteer using conventional abdominal ultrasound scanning procedure and with ROBUST respectively. The study will be done in 2 phases, separated by at least a 1-month interval between scans.
Phase 1: Scanning of volunteer using conventional abdominal ultrasound scanning procedure.
Phase 2: Scanning of volunteer using ROBUST. Outcome measures will include ultrasound image quality, sonographer feedback and comfort level as well as satisfaction feedback from healthy volunteers. A panel of 4 reviewers, consisting of 2 radiologists and 2 senior radiographers will be invited to grade the images, using a 3-point Likert scale. The duration of each scanning will be recorded. The comfort level reported by sonographers will be assessed using the SGH Comfort Level Survey. In addition, the comfort level of healthy volunteers will also be assessed using a satisfaction questionnaire.
Descripción general del estudio
Estado
Descripción detallada
- 10 participating sonographers will be recruited from SGH and SKH to perform abdominal ultrasound scanning.
- 10 healthy volunteers of average body habitus with BMI <30, abdominal circumference <102cm will be recruited.
- Each sonographer will be randomly assigned to scan 1 healthy volunteer. The same volunteer will be scanned twice with an interval of at least 1 month between two scans: once using conventional abdominal ultrasound scanning procedure and once using ROBUST.
- During the session, markers coated with a retroreflective material to reflect light to the motion capture camera will be pasted on participating sonographers on various parts of the upper limb.
- Surface electromyography (sEMG) electrodes will be affixed on sonographers' upper trapezius, deltoid, biceps, triceps, wrist extensors and flexors to monitor muscle activities.
- The healthy volunteer will lie on a plinth with the participating sonographer seated next to him/her. The sonographer will then perform scanning on various abdominal organs following the point of reference and scanning approach as indicated.
- The same ultrasound scanner and probe type will be used on all volunteers by all sonographers.
- Static bilateral grip strength of participating sonographers will be measured using a dynamometer before and after each scan.
- At the end of both scans, participating sonographers will be required to complete a survey on comfort level.
- At the end of both scans, healthy volunteers will be required to complete a survey on satisfaction level.
- The quality of the images from both scans will be rated by 4 readers: 2 consultant radiologists and 2 senior radiographers. A photometer will be used to ensure all readers interpret images directly from a designated monitor under consistent lighting condition.
Tipo de estudio
Inscripción (Actual)
Contactos y Ubicaciones
Ubicaciones de estudio
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Singapore, Singapur, 169608
- Singapore General Hospital
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Singapore, Singapur, 544886
- Sengkang General Hospital
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Método de muestreo
Población de estudio
Descripción
Inclusion Criteria:
Sonographer:
-Experienced sonographers/ radiographers with more than 5 years of experience
Healthy volunteer:
- Inclusion criteria: - BMI <30
- Abdominal circumference <102cm
Exclusion Criteria:
Sonographer:
-Participating sonographers with previously reported work-related or non-work related musculoskeletal discomfort or injury
Healthy volunteer:
-Pregnancy
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
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Comparison of quality of ultrasound image for manual scanning and robot scanning
Periodo de tiempo: During the scan
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During the scan
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Kinematic data, Range of Motion from motion capture system
Periodo de tiempo: During the scan
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During the scan
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Muscle activation from EMG data
Periodo de tiempo: During the scan
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During the scan
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Static bilateral grip strength
Periodo de tiempo: Immediately before the scan and immediately after the scan
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Immediately before the scan and immediately after the scan
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Questionnaire on comfort level from sonographers
Periodo de tiempo: immediately after the scan
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immediately after the scan
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Questionnaire on Satisfaction level from healthy volunteers
Periodo de tiempo: immediately after the scan
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immediately after the scan
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Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
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
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 2017/3049
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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