RecruitingNot ApplicableNCT07264400

Impact of Physical Activity During Pregnancy on Cardiac Variability in Newborns


Sponsor

University Hospital, Clermont-Ferrand

Enrollment

100 participants

Start Date

Oct 15, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Ancillary study of the PregMouv study which aims to evaluate an intervention allowing the best adherence of women in terms of physical activity. Several types of interventions are therefore planned in this study: no intervention, physical activity sessions in person, by videoconference or mixed (in person and videoconference) with accelerometer assessment of the level of physical activity practiced (in the form of energy expenditure, in MET). Thus, for our ancillary study, a comparison of the cardiac variability of newborns will be carried out according to the level of physical activity practiced by the mother regardless of the intervention she benefited from within the framework of the PregMouv study. A comparison of the average saturation and the time spent below 90% saturation will be carried out via a continuous recording of saturation by oximetry. A longitudinal follow-up for the assessment of height and weight growth (from growth curves) and neurodevelopment (by clinical examination and self-questionnaire) is also planned until the child is 2 years old.


Eligibility

Min Age: 1 DayMax Age: 3 Days

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Heart rate variability and Pulmonary function for people with newborn infant. The study is currently recruiting participants at 1 location. People eligible for this study include aged 1 Day to 3 Days.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERHeart rate variability

A Holter ECG recording will be performed on the child's second night for a minimum of 6 hours.

OTHERPulmonary function

Oximetry recording will be performed on the child's second night for a minimum of 6 hours.


Locations(1)

CHU de Clermont-Ferrand

Clermont-Ferrand, France

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NCT07264400


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