Actively Recruiting

Age: 18Years +
FEMALE
Healthy Volunteers
ID06844019

Birth & Breastfeeding Support Study

Led by Herlev Hospital · Updated on 2025-05-28

1628

Participants Needed

1

Research Sites

51 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to understand how certain birth practices and conditions affect exclusive breastfeeding. It focuses on events like cesarean section, vacuum assisted birth, gestational diabetes, and preeclampsia. The main question is whether these factors influence exclusive breastfeeding three months after birth. The study is observational and involves participants who intend to breastfeed and meet specific criteria. Participants are grouped based on birth types and conditions: cesarean section, vacuum assisted birth, gestational diabetes, or preeclampsia. They respond to a series of eight online surveys, one before birth and seven after birth, scheduled at three, seven, and fourteen days; as well as one, three, six, and twelve months postpartum. During the study, participants complete surveys to provide information on their breastfeeding practices over time. Researchers will measure exclusive breastfeeding status at three months as the primary outcome. The study includes follow-up through multiple timepoints extending up to one year after birth. It is sponsored by Herlev Hospital and welcomes adult female participants who plan to breastfeed.

CONDITIONS

Brief Title

Birth & Breastfeeding Support Study

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years or older
  • Intention to breastfeed
  • Expecting a single baby (single gestation)
  • Reads and understands Danish
Not Eligible

You will not qualify if you...

  • Twin gestation (expecting twins)
  • Younger than 18 years
  • No intention to breastfeed
  • Does not read or understand Danish

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 3 months postpartum

Participants are observed through birth and breastfeeding to assess outcomes based on different birth conditions.

Visits aligned with routine care up to 3 months after birth

Trial Site Locations

Total: 1 location

1

Herlev & Gentofte University Hospital

Herlev, Denmark, 2730

Actively Recruiting

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Research Team

D

Dorrit Vizel-Schwartz, MSN, CNM, IBCLC, Ph.d.-student

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

4

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