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Clinical Trials/NCT00145834
NCT00145834CompletedPhase 1

A Randomised Community Based Experimental Trial in the Health Visitor's Practice Field

University of Aarhus2 sites in 1 country1,456 target enrollmentStarted: February 2004Last updated:
Conditions

Trial Snapshot

Phase
Phase 1
Status
Completed
Enrollment
1,456
Locations
2
Primary Endpoint
Breastfeeding duration

Study Overview

Brief Summary

The purpose of this study is to investigate if a postnatal public health breastfeeding intervention relying on the importance of the psychosocial factors can prolong the period with exclusive breastfeeding duration among mothers who want to breastfeed.

Detailed Description

Breastfeeding is a complex learned behaviour and not a capability which comes naturally with motherhood. Different types of professional recommendations have been used to support the new mother in this process.

Randomised studies have shown that postnatal support can influence the breastfeeding duration positively. Various studies has offered different kinds of interventions with home visits and/or telephone calls as the generally used approach, but the proper follow-up on the breastfeeding support in the postnatal period after the mother leaves the hospital is not yet clear.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
0 Years to — (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Danish mother, single child, gestational age of not less than 37 full weeks

Exclusion Criteria

  • Mothers with an ethic background other than Danish, preterm delivery,twin birth

Outcomes

Primary Outcomes

Breastfeeding duration

Secondary Outcomes

  • Satisfaction with the breastfeeding period

Investigators

Sponsor Class
Other

Study Sites (2)

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