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Clinical Trials/NCT02520167
NCT02520167CompletedNot Applicable

Partnership to Improve Nutrition and Adiposity in Prenatal Clinical Care: a Pilot and Feasibility Study

University of Colorado, Denver1 site in 1 country20 target enrollmentStarted: October 1, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
20
Locations
1
Primary Endpoint
Gestational weight gain

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

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

Arms & Interventions

Dietary and Lifestyle Counseling

Experimental

Women randomized to the intervention group will meet with a dietary counselor for 15 minutes at every prenatal appointment. They will receive a dietary and lifestyle curriculum based on the Diabetes Prevention Program curriculum (11 lessons) with one additional lesson providing prenatal breastfeeding education. They will also have access to a private online Facebook page for additional education and peer group support.

Intervention: Dietary and Lifestyle Counseling (Behavioral)

Standard of Care

No Intervention

Usual prenatal care consists of regular clinical appointments, pregnancy ultrasounds, and recommendations to use prenatal multivitamins, eat a balanced diet, and remain physically active. Women with a pre-pregnant body mass index > 30 complete early glucose screening (as early as possible after presentation at the clinic) to detect pre-existing diabetes, and all women undergo routine gestational diabetes screening at 24-28 weeks. Women who test positive for pre-existing diabetes or gestational diabetes are referred to a registered dietitian.

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)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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