Improving Artificial Intelligence-derived Algorithms for Estimating Length and Weight in NEonateS and infanTs up to 6 Months of Age (NEST)
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Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- Это наблюдательное исследование: исследуемое лечение участникам по протоколу не назначают.
- Кому может быть актуально
- Состояния в реестре: Growth, Neonates, AI (Artificial Intelligence). Базовые параметры: 0 Days — 6 мес. · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Сингапур
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
Improving Artificial Intelligence-derived Algorithms for Estimating Length and Weight in NEonateS and infanTs up to 6 Months of Age
Обзор
The NEST study is a prospective, observational research study designed to collect clinical measurements and image data to develop and evaluate artificial intelligence (AI)-derived algorithms for estimating anthropometric parameters in neonates and young infants. The study focuses on infants from birth up to 6 months of age and aims to assess the accuracy of AI-based estimations of length, weight, and head circumference using photographs and/or video recordings captured during routine clinical care. These AI-derived measurements will be compared against standard clinical measurements obtained by trained healthcare professionals in neonatal and infant care settings.
Подробное описание
The NEST study is a prospective, observational cohort study designed to collect paired clinical reference measurements, image data, and associated clinical information to support the development and proof-of-concept evaluation of artificial intelligence (AI)-based algorithms for estimating anthropometric parameters in neonates and young infants.
Standard clinical anthropometric measurements-including infant length, weight, and head circumference-are obtained by trained healthcare professionals in accordance with site-standard clinical procedures and established neonatal measurement practices. These measurements serve as the clinical reference standard for comparison with AI-derived estimates. All reference measurements collected as part of routine clinical care during the study period may be recorded.
In parallel with clinical measurements, non-invasive image data consisting of two-dimensional photographs and/or video recordings of the infant are captured using digital imaging devices. Image capture occurs under real-world clinical conditions and does not require additional physical contact beyond routine care. Image and video data may be collected at multiple timepoints for a given participant, including repeated assessments during hospitalization or follow-up, where applicable. Image-based measurements are not used for clinical decision-making.
AI-derived estimates are compared against standard clinical reference measurements using predefined analytical accuracy and agreement metrics.
Secondary and exploratory objectives include the evaluation of AI models for additional anthropometric parameters, such as weight and head circumference, as well as assessment of the feasibility of image capture in neonatal and infant care settings. Investigator- and parent-reported perceptions related to the usability and acceptability of image-based measurement approaches are also evaluated.
For participants with laboratory test results obtained as part of routine clinical care, selected laboratory values may be recorded. In a subset of participants, additional image data may be collected to support exploratory research related to AI-based estimation of iron status. No additional laboratory testing is performed as part of the study.
Questionnaire-based feedback is collected from investigators and parents or caregivers on the image capture process and to define acceptable ranges of differences between AI-derived estimates and standard clinical measurements. and/or experiences and perceptions related to the use of AI-powered digital tools for monitoring infant growth parameters and health.
All study data are coded prior to analysis. Image data and clinical measurements are linked using study-specific participant identifiers. No facial recognition or identity verification is performed. Data are stored, processed, and analyzed in accordance with approved data protection and confidentiality measures and applicable regulatory requirements.
Первичные конечные точки
- To evaluate the accuracy of the algorithm to estimate length (in cm) [Срок оценки: From enrolment (after informed consent) until discharge from NICU/SCN, up to a maximum of 10 weeks]
Вторичные конечные точки (1)
- To evaluate the mean absolute error of the algorithm to estimate weight (in kg) [Срок оценки: From enrolment (after informed consent) until discharge from NICU/SCN, up to a maximum of 10 weeks]
Критерии участия
Критерии включения
- Infants up from birth up to 6 months of postnatal age (including neonates) who have been admitted to the NICU or SCN at the time of screening
- Parent(s) should be able to comprehend the content of the study and be willing for their child to undergo video and photo recording, and to allow access to their blood sampling results (haemoglobin) taken as part of standard clinical practice
- Written consent from parents and/or legally acceptable representative
Критерии исключения
- Infants who were born with gestational age of less than 28 weeks of gestational age
- Infants who are intubated (i.e., endotracheal, nasotracheal intubation) at the time of screening
- The investigator considers for any reason that the participant would not be suitable for the study
- The participant has an existing medical condition that would prevent standardised measurement of length and/or head circumference e.g. structural abnormality of the lower limbs, orthopaedic conditions, hydrocephalus
- Employees and/or children/family members or relatives of employees of Danone Global Research \& Innovation Center, Danone Asia Pacific Holdings Pte Ltd, or the participating site
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Дизайн исследования
- Модель наблюдения
- Когортное
Центры проведения
Сингапур · 1 центр
- KK Women's and Children's Hospital — Singapore
Идентификаторы
NCT: NCT07514182 · 25REX0090391