KK Women's and Children's Hospital
Singapore
Location status: Recruiting
Location contact
Bin Huey Quek, MBBS
CONTACT
NCT Number: NCT07514182
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.
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All sexes
Observational
Singapore
Location status: Recruiting
Bin Huey Quek, MBBS
CONTACT
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.
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: From enrolment (after informed consent) until discharge from NICU/SCN, up to a maximum of 10 weeks
The primary outcome is the proof-of-concept accuracy of an artificial intelligence (AI)-based algorithm for estimating infant length in a neonatal intensive care unit (NICU) or special care nursery (SCN) setting. AI-derived length estimates (in centimeters) obtained from supine images and/or videos are compared with standard clinical length measurements performed by trained investigators using World Health Organization (WHO)-recommended techniques. Accuracy is evaluated using a composite metric that includes bias, mean absolute error, mean absolute percentage error, and the distribution of absolute percentage errors at predefined thresholds.
Time frame: From enrolment (after informed consent) until discharge from NICU/SCN, up to a maximum of 10 weeks
The secondary outcome is the proof-of-concept accuracy of an artificial intelligence (AI)-based algorithm for estimating infant weight in a neonatal intensive care unit (NICU) or special care nursery (SCN) setting. AI-derived weight estimates (in kilograms) generated from supine images and/or videos are compared with standard clinical weight measurements obtained by trained investigators using World Health Organization (WHO)-recommended techniques. Accuracy is assessed using a composite metric that includes bias, mean absolute error, mean absolute percentage error, and the distribution of absolute percentage errors at predefined thresholds.
Time frame: From enrolment (after informed consent) until discharge from NICU/SCN, up to a maximum of 10 weeks
The exploratory outcome evaluates the proof-of-concept accuracy of an artificial intelligence (AI)-based algorithm for estimating infant head circumference in a neonatal intensive care unit (NICU) or special care nursery (SCN) setting. AI-derived head circumference estimates obtained from images and/or videos are compared with standard clinical head circumference measurements performed by trained investigators using World Health Organization (WHO)-recommended techniques. Accuracy is assessed descriptively using appropriate error metrics to explore the feasibility and potential clinical utility of image-based AI estimation methods.
Time frame: Once per participant, prior to discharge from NICU/SCN (at the conclusion of study participation) [1 day]
Investigator's assessment on the ease of collecting the images
Time frame: Per participant, at the conclusion of study participation (prior to discharge from NICU/SCN) [1 day]
The expected level of accuracy for the anthropometric measurements for length
Time frame: At enrolment or when routine clinical haemoglobin results become available during the NICU/SCN stay (single time point) [ 1day]
This exploratory outcome evaluates the proof-of-concept (POC) accuracy of an artificial intelligence (AI)-based algorithm for estimating haemoglobin levels (Iron AI) in a neonatal intensive care unit (NICU) or special care nursery (SCN) setting. AI-derived haemoglobin estimates (g/dL), generated from images and/or videos collected as part of the study, are compared with haemoglobin values obtained from standard venous blood sampling performed as part of routine clinical care. Accuracy is assessed using a composite metric including bias, mean absolute error, mean absolute percentage error, and predefined percentiles of absolute percentage error. This outcome is exploratory and descriptive in nature.
Contact information is provided by the study sponsor or research team.
Amilia Sng, Senior Digital Health R&I Study Manager, MSc Pharmacology
CONTACT
Kimberley Tan, Clinical Research Associate, BSc
CONTACT
Danone Asia Pacific Holdings Pte, Ltd.
Industry
Improving Artificial Intelligence-derived Algorithms for Estimating Length and Weight in NEonateS and infanTs up to 6 Months of Age
Acronym: NEST
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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