Early Breastfeeding Cessation - is It Possible to Prevent?
This study has been completed.
Sponsor:
University of Aarhus
Collaborators:
Lundbeck Foundation
Sygekassernes Helsefond
Ringkjobing Amt
Ribe Amt
Information provided by:
University of Aarhus
ClinicalTrials.gov Identifier:
NCT00145834
First received: September 1, 2005
Last updated: NA
Last verified: September 2005
History: No changes posted
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Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
Breastfeeding Practice Maternal Behaviour Self-Efficacy |
Behavioral: community based trial |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Prevention |
| Official Title: | A Randomised Community Based Experimental Trial in the Health Visitor's Practice Field |
Resource links provided by NLM:
Further study details as provided by University of Aarhus:
Primary Outcome Measures:
- Breastfeeding duration
Secondary Outcome Measures:
- Satisfaction with the breastfeeding period
| Estimated Enrollment: | 1456 |
| Study Start Date: | February 2004 |
| Estimated Study Completion Date: | April 2005 |
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.
Eligibility| Ages Eligible for Study: | Child, Adult, Senior |
| Genders Eligible for Study: | Both |
Criteria
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
Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study.
To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below.
For general information, see Learn About Clinical Studies.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00145834
Please refer to this study by its ClinicalTrials.gov identifier: NCT00145834
Locations
| Denmark | |
| Institute of Publich Health, Department of Nursing Science, University of Aarhus | |
| Aarhus, Denmark, DK-8000 Aarhus C | |
Sponsors and Collaborators
University of Aarhus
Lundbeck Foundation
Sygekassernes Helsefond
Ringkjobing Amt
Ribe Amt
Investigators
| Study Director: | Ingegerd Harder, Ph.D. | Department of Nursing Science, University of Aarhus |
More Information
| ClinicalTrials.gov Identifier: | NCT00145834 History of Changes |
| Other Study ID Numbers: | SUN-2002-653 |
| Study First Received: | September 1, 2005 |
| Last Updated: | September 1, 2005 |
| Health Authority: | Denmark: National Board of Health |
Keywords provided by University of Aarhus:
|
psychosocial factors breastfeeding postnatal intervention health visitor |
ClinicalTrials.gov processed this record on September 28, 2016