Partnership to Improve Nutrition and Adiposity in Prenatal Clinical Care: a Pilot and Feasibility Study
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Pregnancy
- Sponsor
- University of Colorado, Denver
- Enrollment
- 20
- Locations
- 1
- Primary Endpoint
- Gestational weight gain
- Status
- Completed
- Last Updated
- 8 years ago
Overview
Brief Summary
This study will pilot and assess feasibility of a prenatal intervention for obese pregnant women based on the Diabetes Prevention Program (DPP). Intervention group participants will meet with a clinic dietitian for 15 minutes at every prenatal appointment to complete a DPP-based curriculum and receive breastfeeding education. Control group participants will receive usual prenatal care. Outcomes include reach and dose of the intervention, gestational weight gain, dietary intake, physical activity, and breastfeeding in the first 6 weeks postpartum.
Detailed Description
This study will pilot and test feasibility of a prenatal lifestyle intervention designed to limit gestational weight gain and prevent gestational diabetes. The intervention is based on the Diabetes Prevention Program lifestyle intervention, will include prenatal breastfeeding education and online peer group support, and will be integrated into the participants' regular prenatal appointments. Women (n=24) will be enrolled in early pregnancy. After baseline assessments (demographics, maternal diet, physical activity, mental health), women randomized equally to the intervention or usual care conditions. Further data collection will occur at approximately 24 weeks gestation, 36 weeks gestation, and 6 weeks postpartum, and clinical data (weight, pregnancy and obstetric complications) will be abstracted from medical records at the end of the study. Outcomes include reach and dose of the intervention, gestational weight gain, dietary intake, physical activity, and breastfeeding in the first 6 weeks postpartum. The investigators hypothesize that the intervention will reduce gestational weight gain, improve maternal dietary intake, increase total energy expenditure, and increase breastfeeding exclusivity in the first 6 weeks postpartum.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Singleton pregnancies of \<12 weeks gestation
- •Pre-pregnant body mass index \>=30
- •Speak and understand English
- •Plan to continue care at the clinic through pregnancy and postpartum
Exclusion Criteria
- •Pre-existing diabetes
- •History of serious chronic illnesses
- •History of prior gestational diabetes
- •Prior delivery at \<37 weeks gestation
- •Prior delivery of infant weighing \<2500g
Outcomes
Primary Outcomes
Gestational weight gain
Time Frame: 40 weeks
Weight change from pre-pregnancy to time of delivery
Secondary Outcomes
- Maternal fruit intake(Assessed from 12 weeks gestation through 6 weeks postpartum)
- Maternal vegetable intake(Assessed from 12 weeks gestation through 6 weeks postpartum)
- Maternal added sugars intake(Assessed from 12 weeks gestation through 6 weeks postpartum)
- Maternal whole grains intake(Assessed from 12 weeks gestation through 6 weeks postpartum)
- Maternal solid fats intake(Assessed from 12 weeks gestation through 6 weeks postpartum)
- Maternal physical activity(Assessed from 12 weeks gestation through 6 weeks postpartum)
- Exclusive breastfeeding(Assessed at 6 weeks postpartum)