Breastfeeding Clinical Trial
Official title:
Preparing Mothers for Feeding Their Newborns: A Self-Guided Program for Pregnant Women
This intervention would be a series of self-help-style educational and motivational activity
sheets for patients to complete independently. This will be a randomized clinical control
trial.
Subjects will complete a pre delivery questionnaire and a postpartum questionnaire. Subjects
in the intervention arm will complete 3 activity sheets prenatally during their wait time at
the clinic. The first worksheet can be completed the day of recruitment after consent is
signed.
Subjects will be contacted by phone at 3 and 6 months postpartum to assess long term duration
of breast feeding.
As the benefits of human milk become evident, the investigators are striving to improve the
breastfeeding (BF) rate among new mothers. In April and May of 2014, 73 (71%) of well babies
received human milk at discharge from our postpartum unit, with 40 (35%) and receiving human
milk exclusively. In the neonatal intensive care unit, 83 (89%) received human milk during
those months.
Many of the patients at the teaching institution share risk factors for failure to BF,
including poverty, obesity, unplanned pregnancy and being African American. Efforts have had
limited effect in improving initiation and duration among these patients.
Studies examining the efficacy of various modalities of antenatal education produced modest
results in improving initiation and duration of BF. Several studies examined group BF
education versus routine prenatal care without significant differences in initiation,
exclusivity (the practice of using human milk exclusively and not supplementing with formula)
or duration. Conversely, other study showed a difference in initiation with group education
and showed a difference in exclusivity. Formalized education compared to routine clinical
practice education did not result in a difference in exclusivity in several studies and
neither did a program that included a video showed a difference in initiation with formal
education.
A few studies compared peer counseling to routine prenatal care. One small study of 59 women
found an increase in initiation rate, while a larger study of 2511 women did not find a
difference in initiation or duration.
Other studies found no significant difference in initiation, duration or exclusivity with an
educational program on practical BF skills nor a program on BF attitudes. A small study that
paired BF education with material incentives increased exclusivity. Three studies comparing
interventions by lactation consultants found no difference in initiation or duration,
although one study showed improvement in exclusivity. Postpartum BF self-efficacy correlates
with BF duration and two studies showed improvement in exclusivity with a BF class based on
principles of self-efficacy. These studies based their intervention on Bandura's theory of
self-efficacy, which proposes that an individual's expectation of personal efficacy will
determine her initiation of coping behavior, effort expenditure and duration of persistence.
This theory recognizes four components that contribute to an individual's sense of self-
efficacy, and these include performance accomplishment, vicarious, or social, experience,
verbal persuasion and psychological state. developed a validated scale at measuring prenatal
maternal self-efficacy in breastfeeding.
These two studies used a teaching approach that assumes that pregnant women are adults who
are self-motivated and have past experience that shapes their learning and are a component to
their perception of self-efficacy.
Printed self-help materials are appealing as a low cost intervention that could be widely
implemented. Furthermore, a large study among pregnant women showed that a self-help guide
that is particularly tailored towards pregnant women could be effective in promoting another
healthy behavior modification: smoking cessation. Potentially this method could be effective
when used to prepare mothers for breastfeeding.
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