BMJ open · 2026
Measurement of heart rate and respiratory rate using remote photoplethysmography in paediatrics: a prospective comparative trial protocol - 'rMonitoped1'.
СтатьяСравнительное исследованиеНазвание и аннотация: Перевод в очереди
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Haas-Ferrua Sébastien, Giaccardi Hugo, Ancey Barbara, Freyssinet Emma, Baranton Emma, Joulie Aline, Bendimerad Imad, Olla Marco, De Oliveira Fabrice, Moussaoui Abdelhak, Boyer Laurent, Fontas Eric, Tran Antoine
Аннотация
INTRODUCTION: Vital signs such as heart rate (HR) and respiratory rate (RR), crucial for clinical assessment, are often challenging to measure in paediatric populations. Remote photoplethysmography (rPPG), a video-based measurement tool, has demonstrated accuracy in adults. The objective of this study is to compare HR and RR measurements obtained using rPPG with those from standard clinical monitoring in a paediatric population.
METHODS AND ANALYSIS: This is a monocentric, prospective study enrolling 600 paediatric participants. Each participant will have standard monitoring electrodes (ECG/impedance) placed on the chest while seated facing a camera for rPPG recording. Simultaneous HR and RR measurements will be recorded over periods of 30 and 60 s using both the standard monitor and the rPPG device. The intraclass correlation coefficient will be calculated to assess agreement between the rPPG and standard monitor measurements.
ETHICS AND DISSEMINATION: The study protocol has been approved by the French Agency for the Safety of Health Products (ANSM (Agence nationale de sécurité du médicament) registration no. IDRCB 2023-A02524-41) and by a French ethics committee (CPP Sud Méditerranée III at 29 August 2024, n°2024-A01324-43). The study's findings will be published in peer-reviewed journals and disseminated at national and international conferences and through press releases.
TRIAL REGISTRATION NUMBER: Clinical Trials Registry (NCT06231654).
METHODS AND ANALYSIS: This is a monocentric, prospective study enrolling 600 paediatric participants. Each participant will have standard monitoring electrodes (ECG/impedance) placed on the chest while seated facing a camera for rPPG recording. Simultaneous HR and RR measurements will be recorded over periods of 30 and 60 s using both the standard monitor and the rPPG device. The intraclass correlation coefficient will be calculated to assess agreement between the rPPG and standard monitor measurements.
ETHICS AND DISSEMINATION: The study protocol has been approved by the French Agency for the Safety of Health Products (ANSM (Agence nationale de sécurité du médicament) registration no. IDRCB 2023-A02524-41) and by a French ethics committee (CPP Sud Méditerranée III at 29 August 2024, n°2024-A01324-43). The study's findings will be published in peer-reviewed journals and disseminated at national and international conferences and through press releases.
TRIAL REGISTRATION NUMBER: Clinical Trials Registry (NCT06231654).