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BreastfeedingNCT05871853

Get the Benefits From the Start. Improving Breastfeeding

An observational study of Breastfeeding, run by Slagelse Hospital at 1 site in Denmark.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Breastfeeding is beneficial for the physical and mental health of mothers and infants alike. Most new mothers in Denmark intend to breastfeed, however, a substantial proportion do not succeed to breastfeed as intended. Read more about this study

Who is it for?
Ages 15 to 100 years, women only
Conditions the study is for
Breastfeeding
What is being tested?
Improved breastfeeding support
How many people
1,600 participants
Where
1 siteDenmark
Study dates
25 May 2023to 31 Dec 2028
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 15 to 100 years
  • Women only
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Women giving birth at Slagelse Hospital and their actual infant

Who may be able to join

  • All women giving birth at Slagelse Hospital and their infants during the study period
  • Age at 15 years and above

Who cannot join

  • families with a planned placement of the infant in a fostercare

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Annemi L Frandsen, MSA contact

+4522704247

alfr@regionsjaelland.dk

Maren Rytter, Ph.d. contact

+4527280484

mjry@regionsjaelland.dk

Denmark1 site, 1 recruiting
  • Slagelse Hospital

    Slagelse, 4200

    Annemi L Frandsen, MSA, +4522704247, alfr@regionsjaelland.dk

    Maren Rytter, Ph.d., +4527280484, mjry@regionsjaelland.dk

    Recruiting

Other trials in Denmark

About this study

Official title: Getting the Benefits From the Beginning. Improving Breastfeeding Support for Families at Risk of Breastfeeding Difficulties

Breastfeeding is beneficial for the physical and mental health of mothers and infants alike.

Most new mothers in Denmark intend to breastfeed, however, a substantial proportion do not succeed to breastfeed as intended.

Read more

In Region Zealand, few women breastfeed than in the rest of Denmark in which may be related to a higher proportion of women being overweight, having socio-economic constraints and a low educational level, all associated with breastfeeding difficulties. There is limited knowledge on how to deliver a tailored support aimed at families at high risk of breastfeeding difficulties in a high-income country.

We plan to conduct a study aiming to strengthen breastfeeding support to families at risk of breastfeeding difficulties, delivering at Slagelse Hospital, across healthcare sectors, including obstetric and neonatal departments, primary care and civil society.

The study aims to develop, implement, and evaluate a supportive breastfeeding intervention with specific focus on families at high risk of complicated breastfeeding and early breastfeeding cessation - a prospective cohort study in Region Zealand, Denmark.

Potentially, results can help reducing inequality in health thus more families achieve exclusive breastfeeding and gain health benefits from breastfeeding

Read the detailed description

Background. Breastfeeding is a tailored nutrition for newborn infants in their first years. Breastfeeding has short and long-term positive health effects on both mothers and infants.

For infants, breastfeeding has a protective effect against sudden infant death, respiratory, gastrointestinal and ear infections, obesity, diabetes and childhood leukemia. Breastfeeding also benefits the infant's cognitive development. Studies have found that breastfeeding positively affects the infant's cognitive abilities and IQ. For premature infants, mothers' own milk also protects against the potentially life-threatening disease necrotizing enterocolitis as well as reducing the risk of retinopathy of prematurity for very preterm infants.

For mothers, breastfeeding carries a reduced risk of type 2 diabetes, breast- and ovarian cancer and reduce the risk of cardiovascular disease and benefits the mothers because it may reduce depression and stress. Furthermore, breastfeeding may increase a secure mother-infant attachment, and improve the mother's emotional response to the infant, proportionally with the duration of breastfeeding.

The World Health Organization(WHO) recommends exclusive breastfeeding for six months and partially for two years or longer and has set a goal of optimizing breastfeeding in 2025. Danish Health Authorities also recommend exclusive breastfeeding for six months and partially for one year or longer.

Internationally breastfeeding rates and duration has declined and Denmark is no exception. Breastfeeding has a social barrier both in the early phase of initiation and in the first months, in low-income as well as in high-income countries. We know that breastfeeding follows a pattern of inequalities, and women with less education and low socio-economic status are less likely to exclusively breastfeed.

Declining rates of breastfeeding are a growing problem, as exclusive breastfeeding has decreased over the last decade in all Danish regions. Region Zealand is one of the regions with the lowest rate of exclusive breastfeeding when the infant is four months old compared to the rest of Denmark. Even though Denmark has a relatively well developed health care system with (at least formal) equal access to health services, inequality in health is growing, especially in Region Zealand.

Certain factors are known to be associated with difficulties in initiating and sustaining breastfeeding. These include maternal overweight, gestational diabetes, delivery by cesarean section, admission of the infant to Neonatal Intensive Care Unit (NICU) due to being small, premature or sick, as well as breastfeeding problems with a previous child, previous operations on the breast, social and economic constraints and psychosocial problems for the mother.

In Denmark, we have guidelines for breastfeeding counselling after uncomplicated birth. We know that early interventions will change the trajectory of non-infectious diseases. We lack, however, knowledge on how to offer differentiated care for breastfeeding mother and infant dyads with risk factors for complicated breastfeeding, including how we can improve collaboration with healthcare visitors in the municipalities to make the best transition from hospital to home. We do not have differentiated programs so we help the families who need help the most.

Purpose and hypotheses. This study aims to develop, implement and assess the effect of cross-sectoral cooperation aiming to support breastfeeding in families who give birth at Slagelse Hospital and who are at high risk of complicated breastfeeding. We intend to set up a new service where we provide families at high risk of complicated breastfeeding, with differentiated, practical counselling based on the family's needs, and evidence-based knowledge.

Our hypothesis is that an early differentiated and locally adapted intervention will increase the initiation rate and duration of breastfeeding among women delivering at Slagelse Hospital.

The study is an independent part of an initiative at Slagelse Hospital, Region Zealand, aiming to reduce inequality in health among children.

The study design is a clinical prospective observational cohort study: The development, implementation, and evaluation of a supportive breastfeeding intervention with specific focus on families at high risk of complicated breastfeeding and early breastfeeding cessation - a prospective cohort study in Region Zealand, Denmark.

Aim. To develop, implement and evaluate a locally adapted and differentiated breastfeeding-counselling model, focusing especially on families at risk of experiencing breastfeeding difficulties, and therefore most likely to benefit from health-promoting efforts like breastfeeding support.

Research question. Will the implementation of a locally adapted intervention aimed at supporting families at high risk of complicated breastfeeding outcomes lead to an increase in the proportion of exclusively breastfed children at four months of age when compared to a cohort born before the intervention?

Study design. In a prospective, observational design, we will follow families delivering during eight months following the implementation of the intervention and compare to a control group of families delivering during eight months before the intervention.

Intervention. The intervention is a complex process and we will therefore use a theoretical framework for complex interventions developed by the Medical Research Council, as a sustainable effort for breastfeeding, requires collaboration across sectors, the involvement of various health professions and the involvement of users and stakeholders from the local community.

The exact design of the intervention will therefore be determined according to the results of this process.

However, the intervention is likely to include components described in the WHO's Baby Friendly Hospital Initiative (BFHI) and neonatal BFHI:

We plan to stratify the intervention by identifying women at risk either at prenatal consultations during pregnancy, or at birth:

  1. Women with low risk factors will be given the care described in Danish National Guideline for initiation of breastfeeding after an uncomplicated birth
  2. Women with a moderate risk will be offered a seven day program with easy contact to the maternity ward as described by the Danish Health Authorities in the early postpartum period
  3. Women with high risk will be offered a tailored intervention with an easy access to qualified breastfeeding counselling. This service will be planned in co-creation with peer support groups from the organization "Forældre og Fødsel", midwives and nurses at the Slagelse hospital maternity ward, nurses at the Slagelse hospital neonatal ward, and health visitors from three municipalities in Region Zealand.

Although the intervention has a specific focus on those in the highest risk, it may also improve the care given to families at lower risk of breastfeeding complication by raising general awareness and improving the knowledge among health care workers.

Materials and methods. We will perform a prospective observational cohort study, following families giving birth during the eight months before the intervention (pre-cohort), compared to a cohort of families giving birth during eight months after the intervention is implemented (post-cohort). Children born during a pilot phase of 4 months between the pre-cohort and the complete implementation of the intervention will not be included in the data collection.

Participants. Primarily the intervention aims at families in a target group of families at high risk of complicated breastfeeding; however, as the intervention may also include a general change of culture and attitude, as well as a general improved training among health staff, it may potentially benefit all families. We will therefore collect data from all families delivering at the hospital, including families in the target group, and from low-risk families delivering at the hospital who give consent to participate in the study (collect data).

Data collection. Data will be collected on all consenting families giving birth at Slagelse Hospital in the period of eight months before the intervention, and one year after. Consent to collect and store patient data will be obtained from families at inclusion.

Data on primary and secondary outcomes will be collected through electronic questionnaires after discharge. If the families do not fill out (in) the questionnaires themselves, they will be contacted by telephone.

Power and sample size estimation. It is assumed that 50% of all women currently breastfeed their child for four months based on the Danish Child Database(18). Showing an increase after the intervention to 57% with a power of 80% and alpha of 0.05 requires that we include 796 families in the control and intervention cohort. This is estimated to be achievable as there are approximately 1,800 births annually Slagelse Hospital. This means that in 8 months there are approximately 1,200 women giving birth, of which 80% are expected to give consent for data collection, corresponding to 960 families.

Conditions
Breastfeeding
Being tested
Improved breastfeeding support
Keywords
Breastfeeding, Infant, Newborn, Post-natal Care
Medical subject headings
Breast Feeding

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Improved breastfeeding supportBehavioural

    Cross-sectoral intervention to improve breastfeeding support among women giving birth at Slagelse Hospital, Region Zealand, Denmark

Study groups in NCT05871853
Study groupRoleWhat they receive
Pre-implementation groupWomen delivering during an eight month period, before the intervention is implemented.
Post-implementation groupWomen delivering during an eight month period, after the intervention is implemented.
Receives: Behavioral: Improved breastfeeding support

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Rate of mother's self-reporting exclusive breastfeeding

    Mothers who are exclusive breastfeeding in the post-implementation group, compared to the pre-implementation group (n/% of total).

    Exclusive breastfeeding is defined as exclusive fed at the breast after discharge from hospital. This means, that in addition to breastfeeding, supplements with water and similar and/or a or a maximum of one meal of breastmilk substitute or mothers expressed breastmilk per week.

    Measured: 4 month postpartum

Secondary outcomes (8)
  1. Duration of exclusive breastfeeding

    Duration of mothers' self-reporting exclusive breastfeeding in the post-implementation group, compared to the pre-implementation group (days, median with IQR).

    Measured: 0-12 month

  2. Duration of any breastfeeding

    Duration of mothers' self-reporting any breastfeeding in the post-implementation group, compared to the pre-implementation group (days, median with IQR).

    Measured: 0-12 month

  3. Rate of exclusive breastfeeding reported by the home-visiting nurse

    Mothers who are exclusive breastfeeding in the post-implementation group, compared to the pre-implementation group. Reported from the Danish National cross-sectoral database at (n/% of total).

    Measured: 4 months

  4. Any admission of the infant

    Any admission of the infant to hospital or referral to a pediatric outpatient clinic compared with any breastfeeding in the post-implementation group, compared to the pre-implementation group (n/% of total).

    Measured: 0-12 month

  5. Mothers self-reported well-being

    Mother's self-reported well-being measured by WHO 5 in the post-implementation group compared to the pre-implementation group. (mean (SD) cut off ><50 indicating clinical depression)

    Measured: Third trimester, 14 days, 1 month, 4 month, 6 month after birth

  6. Infant well-being as reported by the mother

    Mother's selfreported infant health related quality of life (TANDI) in the post-implementation group compared to the pre-implementation group at age of four month.

    Measured: 4 month

  7. Proportion of children sucking at the breast within the first hour of life

    The proportion of children sucking at the breast within the first hour of life, in the post-implementation group compared to the pre-implementation group. Reported by the mother at 14 days postpartum (n/%total).

    Measured: 1 hour of life

  8. Time spend skin-to-skin on 14th day of life

    Time (hours) spend skin-to-skin on the previous day as reported by the mother at 14 days postpartum in the post-implementation group compared to the pre-implementation group (hours/24 hours).

    Measured: Day 13

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 May 2023
  2. Study start25 May 2023
  3. Primary completion15 Oct 2025 (estimated)
  4. Study completion31 Dec 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
1,600 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05871853
Sponsor's protocol ID
REG-094-2022
Status last verified
Jun 2023
First submitted
15 May 2023
Last updated
18 Jun 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: We plan to upload anonymized data to a data repository

Questions about this trial

What is this clinical trial studying?

An observational study of Breastfeeding, run by Slagelse Hospital at 1 site in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 18 Jun 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Annemi L Frandsen, MSA (+4522704247, alfr@regionsjaelland.dk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Rate of mother's self-reporting exclusive breastfeeding (time frame: 4 month postpartum). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Jun 2023.

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