Prenatal Breastfeeding Education to Reduce Nipple Pain (BEST)

This study has been completed.
Sponsor:
Collaborators:
Association of American Medical Colleges
Information provided by:
University of California, Davis
ClinicalTrials.gov Identifier:
NCT01092156
First received: March 22, 2010
Last updated: June 21, 2010
Last verified: June 2010
  Purpose

This study is a randomized controlled trial to evaluate the effectiveness of different approaches to prenatal teaching of infant latch.


Condition Intervention
Nipple Pain During Lactation
Behavioral: Education

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Prevention
Official Title: Prenatal Breastfeeding Education to Reduce Nipple Pain

Resource links provided by NLM:


Further study details as provided by University of California, Davis:

Primary Outcome Measures:
  • Nipple pain day 3 postpartum [ Time Frame: Day 3 postpartum ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Breastfeeding status day 30 postpartum [ Time Frame: Day 30 postpartum ] [ Designated as safety issue: No ]

Enrollment: 200
Study Start Date: January 2007
Study Completion Date: November 2008
Primary Completion Date: November 2008 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Education on Infant-led latching Behavioral: Education
Education on Infant-led latching
No Intervention: Standard education

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Female
Criteria

Inclusion Criteria:

  • Pregnant women who intend to breastfeed their infants
  • Single infant
  • Resides in catchment area
  • Has phone
  • Speaks English
  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: NCT01092156

Locations
United States, California
Sutter Davis Hospital
Davis, California, United States, 95616
Sponsors and Collaborators
University of California, Davis
Association of American Medical Colleges
Investigators
Principal Investigator: Caroline J Chantry, M.D. University of California, Davis
Principal Investigator: Kathryn G Dewey, Ph.D. University of California, Davis
  More Information

No publications provided

Responsible Party: Caroline J. Chantry, University of California, Davis
ClinicalTrials.gov Identifier: NCT01092156     History of Changes
Other Study ID Numbers: 200614137-5, MM-0844-05/05
Study First Received: March 22, 2010
Last Updated: June 21, 2010
Health Authority: United States: Institutional Review Board

Keywords provided by University of California, Davis:
Nipple pain during lactation

ClinicalTrials.gov processed this record on September 22, 2014