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Clinical Trials in Denmark / NCT05311631
Active, not recruiting Not applicable

Breastfeeding - a Good Start Together

NCT05311631 · tracked via the Priya Life Science Denmark tracker
Phase
Not applicable
Started
2022-04-26
Last updated
2026-02-09

Condition(s) studied

BreastfeedingBreastfeeding, Exclusive

Investigational drug(s) / intervention(s)

Breastfeeding support

Breastfeeding support: The core of the intervention is a trustful relation between the health visitor and the families based on principles of needs based communication. Health visitors will enhance parents' action competence based on breastfeeding self-efficacy, focusing on parents' wishes and needs. The breastfeeding support includes four main messages: joint parenting task, skin-to-skin contact, frequent breastfeeding, and good positioning. Training of health visitors includes e-learning and a two-day course with physical attendance. Supportive materials are developed including communicative support tools and a web-page providing support and knowledge when the health visitor is off hours. All families in intervention sites accepting the health visitor program will receive the improved breastfeeding support. Families in the high-risk group are offered an intensified intervention with close follow-up by telephone in planned time-intervals, thus a higher dose of the intervention.

Study summary

The Breastfeeding - a Good Start Together intervention study aims to increase the proportion of women who breastfeed for four and six months, and proportionately more in a group of women who are in risk of early breastfeeding cessation; and thus reduce social inequality of mother and infant health.

Eligibility

Sex
ALL
Min age
15 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: 1a. Families discharged \<72 hours post partum (from 26 April 2022 - 17 January 2023) 1b. Families discharged \< 7 days post partum (from 18 January 2023 onwards due to lower than expected recruitment rate) 2\. Families with intention of breastfeeding Exclusion Criteria: * Insufficient skills in Danish or English language to be able to answer questionnaires and understand interventions conveyed in Danish or English * Families with mothers with known substance abuse or addiction * Families expecting more than one child * Families having delivered preterm, prior to 37 weeks of gestation * Families with mothers or child having difficulty breastfeeding due to a known morbidity or disablement

Primary outcome measure(s)

Trial sites (21)

FacilityCityRegionStatus
Aabenraa Kommune Aabenraa Denmark
Jammerbugt Kommune Aabybro Denmark
Vesthimmerland Kommune Aars Denmark
Assens Kommune Assens Denmark
Billund Kommune Billund Denmark
Esbjerg Kommune Esbjerg Denmark
Fredericia Kommune Fredericia Denmark
Frederikshavn Kommune Frederikshavn Denmark
Haderslev Kommune Haderslev Denmark
Mariagerfjord Kommune Hobro Denmark
Kolding Kommune Kolding Denmark
Middelfart Kommune Middelfart Denmark
Morsø Kommune Nykøbing Mors Denmark
Odense Kommune Odense Denmark
Faaborg-Midtfyn Kommune Ringe Denmark
Svendborg Kommune Svendborg Denmark
Sønderborg Kommune Sønderborg Denmark
Thisted Kommune Thisted Denmark
Tønder Kommune Tønder Denmark
Varde Kommune Varde Denmark
Vejen Kommune Vejen Municipality Denmark

More University of Copenhagen trials in Denmark

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05311631 on ClinicalTrials.gov ↗ ← All trials in Denmark