Lifestyle Intervention to Limit Excessive Weight Gain During Pregnancy in Minority Women
Pregnancy, Weight Gain
About this trial
This is an interventional prevention trial for Pregnancy focused on measuring pregnancy, weight gain, obesity, pregnancy and weight gain
Eligibility Criteria
Inclusion Criteria:
- Blacks and Hispanic
- women between 18-45 years of age;
- 2) overweight and obese (BMI > 25 kg/m2),
- 3) have a sedentary lifestyle (<30 minutes/day of moderate physical activity), and
- 4) prenatal care established at less than 20 weeks of gestation,
- 5) with a singleton pregnancy.
Exclusion Criteria:
- Women with 1) age < 18 or > 45 years,
- 2) > 20 weeks gestation,
- 3) history of diagnosis of type 2 diabetes, hypertension, cardiovascular disease, chronic renal disease, and active liver disease (AST > 3 ULN),
- 4) anemia (hemoglobin < 10 g, hematocrit < 32%);
- 5) current medications which adversely influence glucose tolerance (corticosteroids),
- 6) multiple pregnancy,
- 7) women not planning to continue pregnancy to term, 7) contraindications to participate in regular physical activity,
- 8) patients with mental conditions rendering them unable to understand the nature, scope, and possible consequences of the study
Sites / Locations
- Grady Memorial Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Lifestyle intervention
Standard of care group
Women on the intervention group will participate in a lifestyle program based on diet and moderate physical activity implemented shortly after first recognition of pregnancy. These women will attend monthly nutrition and physical activity educational sessions, and receive booster every 2 weeks.
Patients randomized to the standard of care group will receive counseling routinely provided to all prenatal care women as recommended by the Institute of Medicine for appropriate nutrition and weight gain and ACOG guidelines for appropriate physical activity during pregnancy.