Skip to content

Semi-structured individual interviews and randomized controlled intervention study for the development and evaluation of digital breastfeeding support "HeBa"

Semi-structured individual interviews and randomized controlled intervention study for the development and evaluation of digital breastfeeding support "HeBa" - HeBa

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00027294
Enrollment
1188
Registered
2023-02-07
Start date
2022-06-07
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

breastfeeding promotion breastfeeding support

Interventions

Group 1: From the 34th week of gestation, parents will have access to a web app with elements of breastfeeding promotion and support as well as a forum in which the questions posed by the parents in t

Sponsors

LMU Kliinkum, Dr. von Haunersches Kinderspital; Stoffwechsel und Ernährung
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Months to 6 Months

Inclusion criteria

Inclusion criteria: Interviews: First child; no factors existed that could have interfered with breastfeeding; born on schedule (= 37 weeks gestation and = 41 weeks + 6 days); child was ever breastfed intervention study: First child; no abnormalities to date; no factors on the part of the mother that interfered with or precluded breastfeeding of the infant, e.g., medication; parents living in a joint household.

Exclusion criteria

Exclusion criteria: Interviews: Second or later child in the family; premature birth; factors on the part of the mother or infant that interfere with or preclude breastfeeding e.g. medication, LKS; infant was not breastfed intervention study: Second or later child in the family; fetal abnormality already detected before birth; premature birth; factors on the part of the mother already present before delivery that interfere with or preclude breastfeeding of the infant e.g. medication; parents do not live in 1 common household.

Design outcomes

Primary

MeasureTime frame
Comparing the rate of exclusive breastfeeding 4 months after delivery between the control and intervention groups

Secondary

MeasureTime frame
- The rate of exclusive breastfeeding 6 full months after delivery will be compared between the control and intervention groups - The rate of any breastfeeding 6 full months after delivery will be compared between the control and intervention groups - The results of the questionnaires on intention to breastfeed and confidence in breastfeeding will be compared in relation to the self-efficacy of breastfeeding between the control and intervention groups - The results of the questionnaires on intention to breastfeed and breastfeeding confidence of the control and intervention group will be related to the breastfeeding rate with the question whether a prediction of breastfeeding success can be made on the basis of the answers to this questionnaire - The questions asked by the parents in the forum of the intervention group will be qualitatively evaluated in order to further develop the web app - The user behavior of the participants of the intervention group will be measured and related to the individual breastfeeding behavior as well as the age of the infant - The evaluation of the web app by the participants of the intervention group will be used to further develop the web app

Countries

Germany

Contacts

Public ContactMonika Ziebart

LMU Klinikum, Dr. von Haunersches Kinderspital; Stoffwechsel und Ernährungsmedizin

Monika.Ziebart@med.uni-muenchen.de089440052826

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026