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Assessment of Factors Influencing Parents' Attendance Time During Feeding Time of Premature Infants Born Before 35 Weeks of Amenorrhea in Besançon University Hospital (PréPaLim)

C

Centre Hospitalier Universitaire de Besancon

Status

Completed

Conditions

Premature Birth

Study type

Observational

Funder types

Other

Identifiers

NCT05177913
P/2019/409

Details and patient eligibility

About

The precise description of parental presence and the associated factors will make it possible to construct an intervention in order to correct potentially low parental participation. The demonstration of the effectiveness of such an intervention will be the subject of a larger study (PHRIP type). Ultimately, the investigators want to personalize the daily support for parents to offer optimal support for parenting.

Full description

Considering the importance of the bond of attachment, and in particular the emotional tuning between the adult and the premature baby and the particularly important interactions during feeding, it seemed essential to us to make an evaluation of the parental presence during the meals. , which sheds light on the factors influencing this presence.

The presence time seems to vary depending on: the child's background, the profile of the parents, the profile of the child and environmental factors.

Knowing the factors influencing this presence is essential in order to understand the obstacles to the arrival of parents, to think as a team and to offer personalized support in order to allow them to be more present with their baby.

Enrollment

75 patients

Sex

All

Ages

1 to 10 days old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Premature newborn under 35 weeks of amenorrhea (AS), hospitalized at Besançon University Hospital,
  • Newborn baby whose parents:

expressed their non-opposition to participate in the study, are affiliated to a social security scheme, are of age, express themselves easily in French.

Exclusion criteria

  • Newborn baby whose parents object to participating in the study,
  • Newborns presenting severe malformative anomalies, or malformations of the oral sphere,
  • Newborn baby whose transfer is scheduled before the end of hospitalization (excluding birthing pool at the CHU de Besançon).

Trial contacts and locations

1

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Central trial contact

Boillot Sandrine

Data sourced from clinicaltrials.gov

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