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Benefit of Scarf Support on Skin-to-skin Time and Portage in Neonatology and at Home

Benefit of Scarf Support on Skin-to-skin Time and Portage in Neonatology and at Home(PAPSE)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04034719
Acronym
PAPSE
Enrollment
80
Registered
2019-07-26
Start date
2019-10-08
Completion date
2022-03-22
Last updated
2022-08-24

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

Conditions

Infant, Newborn, Disease

Keywords

Newborn, Parents, Carrying, Skin-to-skin, Scarf

Brief summary

Carrying (or kangaroo carrying) is known to reduce neonatal and child morbidity and mortality and improves the quality of survival of premature and term children during the most fragile growth period, the first thousand days of life. Carrying is also a growing brain protection technique and becomes a routine of care in all neonatal units around the world. In University hospital of Saint-Etienne, the developmental care program has been developed since 2002 in all neonatology units and advocates the practice of skin-to-skin carrying between the parent (father or mother) and his baby, from the time of the hospitalization. Professionals in units who have long been thinking about the concept of attachment and the benefits of skin-to-skin, wish to validate the use of the wearing scarf as a tool for the practice of skin -in-skin in neonatology then back home by performing a randomized monocentric prospective longitudinal study.

Detailed description

This study it's a single-center, prospective, randomized study to evaluate the benefit of the scarf in the practice of skin-to-skin and portage (PAPSE Group) compared to a Skin-to-Skin and Carry Without Scarf (PAP group).

Interventions

OTHERportage scarf

Parents will be carried their newborn with the portage scarf provided by the department.

OTHERusual practice

Parents will be carried their newborn as their usual practice.

Sponsors

Centre Hospitalier Universitaire de Saint Etienne
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 10 Weeks
Healthy volunteers
No

Inclusion criteria

For the child: * Any newborn regardless of gestational age and postnatal age hospitalized in the neonatology department of the University Hospital of Saint-Etienne For the parent (father or mother): * Be a parent of a child eligible for the research protocol

Exclusion criteria

For the child: * Need for sedation or analgesia for the duration of the study * Orthopedic pathology incompatible with the practice of carrying * Other medical contraindications to carriage * Absence of parents For the parent (father or mother): * Family, social or psychological situation compromising the evaluation * No fluency in the French language

Design outcomes

Primary

MeasureTime frameDescription
Number of minuts with portage skin-to-skinFrom inclusion to 2 months after exitMeasured in minutes by the time sheet of presence.

Countries

France

Outcome results

None listed

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