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Cracking the Code of Crying Babies: How Familiarity Changes the Interpretation of Cries

Cracking the Code of Crying Babies: How Familiarity Changes the Interpretation of Cries

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05170178
Acronym
BEBEDOL
Enrollment
62
Registered
2021-12-27
Start date
2022-06-30
Completion date
2023-05-12
Last updated
2023-08-04

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

Conditions

Magnetic Resonance Imaging, Neuronal Activity

Keywords

baby cries, pain, brain responses, fmRI, familiarity

Brief summary

Understanding babies' signals is essential to meet their needs. Recent works suggest that crying provides useful information, not only allowing parents to recognize their baby among others (static information), but also to distinguish between mild discomfort and pain cries (dynamic information). The perception of this information by adults involves a parental brain network including brain areas involved in empathy, attention, emotional regulation, motor as well as regions of the limbic system or associated with the reward network.

Detailed description

This network is involved when listening to cries of familiar babies, or pain cries. How do we become specialist of a baby's cries? To date, no functional imaging study has examined the specific brain activations when listening to the cries of a familiar baby in different situations, particularly painful ones.

Interventions

BEHAVIORALinclusion and familiarization

* presentation of the study purpose and the protocol to the volunteer * clinical examination to check inclusion and exclusion criteria * Familiarization with the crying of one assigned baby, by listening to several bath cries from this baby

BEHAVIORALfMRI acquisition and closure

* Second phase of familiarization, listening again to bath cries of their assigned baby. These cries will be different from those listened during the first familiarization phase. * MRI acquisition: after acquisition of the anatomical images (5 min), the subjects will listen to 64 cries divided into 4 functional MRI sessions of 10 minutes each. The cries will be those of their baby or of unknown babies, evoked in a painful (vaccination) or a non-painful (bath) situation, presented in a pseudo-random order. Participants will be asked to assess whether they recognize their baby (yes/no) and whether they recognize a pain cry (yes/no). * debriefing * Protocol ending

Sponsors

Centre Hospitalier Universitaire de Saint Etienne
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

Group with parental experience caring for infants (20 men and 20 women) Group with professional experience in caring for infants (20 women)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

For all volunteers: * Affiliated or entitled to a social security plan * Right-handed by the Edinburgh laterality test * Having given free, informed and written consent to participate in the study * Having given their consent for the communication of the MRI results to their attending physician Group with parental experience caring for infants : * Men or women between 18 and 50 years old * Parent of a child under 2 years old Group with professional experience in caring for infants * Women between 18 and 50 years old * Without dependent children under 2 years of age * People in daily contact with infants in the professional circle (e.g. nurses, pediatricians, midwives, maternity nurses, etc)

Exclusion criteria

* Pregnant women, parturient, nursing mothers or parents * Persons deprived of liberty, hospitalized without consent, hospitalized for purposes other than research * Minors * Adults under legal protection (guardianship) or unable to express their consent * Subjects with contraindications to the MRI examination: use of a pacemaker or an insulin pump, wearing a metallic prothesis, an intracerebral clip or a piercing, claustrophobia, * Taking medication for less than 12 hours, * Neurological, psychiatric or auditory history or deficits. * Anxiety and/or depressive disorders

Design outcomes

Primary

MeasureTime frameDescription
BOLD signal (blood oxygen level-dependent)during the whole listening sessionMeasurement of the BOLD signal by fMRI (functional magnetic resonance imaging) in adults during listening to natural cries of a familiar baby and unknown babies, in two painful (vaccination) or non-painful (bath) situations.

Secondary

MeasureTime frameDescription
participants'experience at caring for babiesAt the inclusion visitExperience at caring for babies : Yes or No
participants' sexAt the inclusion visitSex : Male or female

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026