View Clinical Trial (Medical Research Study)
Building Social Networks to Enhance Postpartum Weight Loss and Appropriate Infant Feeding Practices - NCT01081340-37211(Clinical Trial 566963)
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Nashville |
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State:
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TN |
| Zip Code: |
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37211 |
| Conditions: |
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Obesity |
| Purpose: |
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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.
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| Study summary: |
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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. |
| Criteria: |
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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 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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July 22, 2010 |
Modifications to
this listing: |
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above to view all information about this clinical trial. |
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