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Understanding Newborn-Mother Synchrony at Home: Feasibility of Remote Monitoring

Understanding Newborn-Mother Synchrony at Home: Feasibility of Remote Monitoring

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07392138
Enrollment
60
Registered
2026-02-06
Start date
2026-04-13
Completion date
2026-05-01
Last updated
2026-04-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Synchrony

Brief summary

Parents and newborns influence each other in a dynamic interaction that can be described as synchrony. Synchrony between a newborn and mother refers to the dynamic and reciprocal adaptation between the newborn and mother. In this synchrony, the mother is highly receptive and sensitive to the newborn's signals, feelings, and needs. The aim of this study is to investigate the physiological and behavioral synchrony between newborns and their mothers, and to investigate the connection between maternal heart rate variability and postpartum depression symptoms in the home environment and to evaluate the suitability of remote monitoring devices for use in the home environment. The study participants consist of 30 newborns and 30 mothers. The inclusion criteria for newborns are: 1) informed consent from the newborn's parents/guardians 2) the newborn's health status has been confirmed as normal during hospital monitoring, and 3) the newborn is less than one month old. The inclusion criteria for mothers are: 1) ability to participate in Finnish, and 2) the mother has access to an Android smartphone. Data collection will be carried out using the following remote monitoring methods: Emfit smart mattress, Zoundream Cry analyses technology, Polar Verity Sense sensor, and Empatica EmbracePlus sensor. In addition, data will be collected using background information forms, a maternal stress scale (PSS-4), a diary completed by the mother, a maternal depression questionnaire (EPDS), and questionnaires measuring the suitability of remote monitoring in the home environment, and a thematic interview. In addition, at the end of the data collection phase, the mothers participating in the study will try out the Companion App, which displays sample data on the well-being of newborns, and respond to a questionnaire on the usability of the app.

Interventions

OTHERUsing monitoring devices

During the data collection, mother and newborn are using the monitoring devices listed in study description.

Sponsors

University of Turku
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
0 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

, mothers: * ability to participate in Finnish * Android smart phone available Inclusion Criteria, newborns: * received informed consent from both parents/guardians * the newborn's health has been stated normal during hospital stay * the newborn is \< 1-month of age

Exclusion criteria

, both (mother and newborn): Not meeting the inclusion criteria

Design outcomes

Primary

MeasureTime frameDescription
Physiological synchrony24 hoursMeasuring correlation between mother heart rate (mHR (unit: BPM)) and heart rate variability (mHRV (unit ms)) and newborn heart rate (bHR (unit: BPM)) and heart rate variability (bHRV (unit: ms)).

Secondary

MeasureTime frameDescription
Behavioral synchrony24 hoursMeasuring the correlation between mother total sleep duration and duration of different sleep stages and newborn total sleep duration and duration of sleep stages (unit: hours and minutes).
Correlation between mother heart rate variability and depressive symptomsDuration of data collection varies from 1 to 4 weeks depending on the mother's decision.Measuring the correlation between mother heart rate variability (mHRV (units: ms)) and depressive symptoms (points from EPDS scale).
Correlation between mother sleep and depressive symptoms.Duration of data collection varies from 1 to 4 weeks, depending on the mother's decision.Measuring the correlation between the duration of mother sleep stages (unit: hours and minutes) and depressive symptoms (points from EPDS scale).

Countries

Finland

Contacts

CONTACTAnna Axelin, Professor
anmaax@utu.fi+358405029905

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 17, 2026