Lactation Education Study in Mothers of Very Low Birth Weight Infants

Sponsor
Wake Forest University Health Sciences (Other)
Overall Status
Completed
CT.gov ID
NCT01167517
Collaborator
Forsyth Medical Center (Other)
40
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2
123
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Study Details

Study Description

Brief Summary

This study will test the effectiveness of breast milk expression discharge instructions in digital video disc (DVD) format for home use by mothers of very low birth weight infants on the dose and duration of mother's breast milk feeding in their infants compared to breast milk expression discharge instructions in printed format. The investigators hypothesize that infants whose mothers receive breast milk expression discharge instructions via DVD will receive a larger dose of maternal breast milk and for longer duration during the initial neonatal intensive care unit hospitalization than infants whose mothers receive discharge instructions in printed format.

Condition or Disease Intervention/Treatment Phase
  • Other: Instructional digital video disc (DVD)
N/A

Detailed Description

Very low birth weight (VLBW; <1500 g) infants who receive maternal breast milk, as opposed to infant formula, are less likely to experience the serious illnesses and poor developmental outcomes associated with VLBW. However, a disparity exists in breast milk feeding. Infants whose mothers have low educational attainment and low income are less likely to receive maternal breast milk than infants whose mothers who do not have low educational attainment and low income. The primary objective of this proposed research is to determine the effect of lactation discharge instructions in an audio-visual format provided to mothers for home viewing on the dose and duration of maternal breast milk received by their VLBW infants during the neonatal intensive care unit hospitalization.

Methods. Forty mothers of VLBW infants will be randomly assigned to receive a breast milk expression instruction digital video disc (DVD) in addition to standard of care lactation education or assigned to receive written instructions in addition to standard of care lactation education. In addition to comparing infant intake of maternal breast milk intake, pre and post intervention lactation and breast milk expression knowledge will be compared between groups and DVD viewing frequency and acceptability will be determined with a log and questionnaire to be completed by the intervention group and collected the first month after delivery.

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Care Provider)
Primary Purpose:
Prevention
Official Title:
Lactation Education Study in Mothers of Very Low Birth Weight Infants
Actual Study Start Date :
Jul 1, 2010
Actual Primary Completion Date :
Apr 9, 2016
Actual Study Completion Date :
Sep 30, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Instructional digital video disc (DVD)

Breast milk expression instructions provided by digital video disc at the time of hospital discharge.

Other: Instructional digital video disc (DVD)
Breast milk expression instructions provided by digital video disc at the time of hospital discharge
Other Names:
  • A Premie Needs His Mother
  • Placebo Comparator: Instructions in print format

    Breast milk expression instructions provided in print format at the time of hospital discharge.

    Other: Instructional digital video disc (DVD)
    Breast milk expression instructions provided by digital video disc at the time of hospital discharge
    Other Names:
  • A Premie Needs His Mother
  • Outcome Measures

    Primary Outcome Measures

    1. Maternal breast milk proportion of enteral feeding. [Daily during the initial hospitalization which is an average of 60 days]

      Volume (ml) of maternal breast milk received daily by the infant divided by the total daily volume of all enteral feeding received.

    2. Volume of daily maternal milk intake in relation to infant weight. [Daily during the initial hospitalization which is an average of 60 days]

      Daily maternal milk intake(ml)divided by daily infant weight (kilograms).

    Secondary Outcome Measures

    1. Maternal lactation and breast milk expression knowledge. [One month postpartum]

      Prior knowledge will be assessed by administering a self-administered knowledge test on lactation and breast milk expression before providing the instructional DVD or written instructions. The same test will be self-administered approximately one month after delivery.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Infant birth weight less than 1500 grams

    • Maternal educational attainment less than/equal to 12 years

    • Maternal low income status (Medicaid participant prior to delivery)

    Exclusion Criteria:
    • Non-English speaking

    • Illicit drug use during pregnancy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Forsyth Medical Center Winston-Salem North Carolina United States 27103

    Sponsors and Collaborators

    • Wake Forest University Health Sciences
    • Forsyth Medical Center

    Investigators

    • Principal Investigator: Paula M Sisk, PhD, Wake Forest Baptist Medical Center/ Forsyth Medical Center

    Study Documents (Full-Text)

    More Information

    Publications

    Responsible Party:
    Wake Forest University Health Sciences
    ClinicalTrials.gov Identifier:
    NCT01167517
    Other Study ID Numbers:
    • IRB00013359
    • FMC 2010.0401
    First Posted:
    Jul 22, 2010
    Last Update Posted:
    Oct 29, 2020
    Last Verified:
    Aug 1, 2020
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Wake Forest University Health Sciences
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 29, 2020