Skip to content

Building Social Networks to Enhance Postpartum Weight Loss and Appropriate Infant Feeding Practices

Building Social Networks to Enhance Postpartum Weight Loss and Appropriate Infant Feeding Practices

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01081340
Enrollment
41
Registered
2010-03-05
Start date
2010-05-31
Completion date
2011-08-31
Last updated
2018-08-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

gestational weight gain, postpartum weight loss, breastfeeding, overfeeding

Brief summary

The purpose of this study is to examine whether we can use social networks to spread health information and health behaviors that 1) support women in returning to their pre-pregnancy weight after delivery; and 2) promote healthy infant feeding practices.

Detailed description

The long-term goal of this research is to prevent obesity-related adverse health outcomes for future generations by applying information emerging from social network studies to the development of new population-based behavioral interventions. There are a number of critical periods during fetal and infant development that appear to influence the later development of obesity. Interventions that prevent insult to these critical windows from occurring could improve children's life course trajectories. This project sets the groundwork for examining whether social networks could explicitly be utilized to prevent obesity from developing by transmitting health information and health behaviors that 1) prevent postpartum weight retention in first time mothers and 2) promote appropriate infant feeding practices. The secondary aim is to assess which individual-level network-related characteristics best predict postpartum body composition and infant feeding practices.

Interventions

Group support and health education sessions weekly during third trimester and once every two weeks until 6 months postpartum

BEHAVIORALHome visit

Three home visits during third trimester and three during postpartum period until 6 months postpartum

Sponsors

American Heart Association
CollaboratorOTHER
Wake Forest University Health Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Latina (self-defined, or born in Central or South America) * Spanish-speaking and/or English-speaking, * 18 years of age or older * less than 24 weeks pregnant * did or did not have a termination of a previous pregnancy before 20 weeks * has not carried a pregnancy to term * normal, overweight or obese (pre-pregnancy BMI \>18.5 and \<39)

Exclusion criteria

* non-Latina, * non-Spanish-speaking or non-English speaking * less than 18 years of age * more than 24 weeks pregnant * had a termination of a previous pregnancy after 20 weeks * multiparous * underweight (pre-pregnancy BMI \< 18.5) * morbidly obese (pre-pregnancy BMI ≥ 39) * currently enrolled in another program that targets weight, physical activity, or nutrition

Design outcomes

Primary

MeasureTime frameDescription
Weight (kg)6 times over 10 monthsgestational weight gain and postpartum weight loss

Secondary

MeasureTime frameDescription
Infant feeding practices3 times over 6 monthsduration of breastfeeding, use of supplemental fluids, overfeeding, timing of the introduction of solids
Social network structure6 times over 10 monthsnumber and type of relationships
Waist Circumference3 times over 6 months
Body composition3 times over 6 monthsBIA postpartum
Nutrition6 times over 10 monthsFat/Fruit/Vegetable intake
Physical Activity6 times over 10 monthsself-report
Depression6 times over 10 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026