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Evaluation of Breastfeeding Support After Short Time Hospitalization

D

Danish Committee for Health Education

Status

Completed

Conditions

Breastfeeding

Treatments

Other: New Breastfeeding Counselling
Other: Treatment as usual

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT01620723
7111442

Details and patient eligibility

About

The purpose of this study is to evaluate if the developed theory and evidence based programme has a positive effect on mother's breastfeeding self efficacy, establishing an effective breastfeeding and breastfeeding duration after short time hospitalization.

Enrollment

3,541 patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion criteria

  • pregnant women (gestational week 35-36)

Exclusion criteria

  • women with known physical, psychological and/or social illness/problem that result in hospitalization more than 50 hours after delivery
  • women with known pregnancy related illness that result in hospitalization more than 50 hours after delivery
  • Women not understanding or speaking Danish
  • women expecting multiple babies
  • women having decided not to breastfeed
  • women expecting to deliver at another hospital than the one she has been visiting during pregnancy

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

3,541 participants in 2 patient groups

New breastfeeding programme
Experimental group
Description:
The breastfeeding programme consists of four core elements: 1. breastfeeding is a parental task 2. skin to skin contact during the first three days 3. frequent breastfeeding at least 8 times a day 4. good positioning, preferable in a laid back position Moreover communication was supposed to enhance breastfeeding self-efficacy, using Banduras theory of self-efficacy
Treatment:
Other: New Breastfeeding Counselling
Treatment as usual
Active Comparator group
Description:
Breastfeeding counselling uses the national handbook of breastfeeding as reference
Treatment:
Other: Treatment as usual

Trial contacts and locations

9

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Data sourced from clinicaltrials.gov

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