Lifestyle Intervention to Limit Excessive Weight Gain During Pregnancy in Minority Women

Guillermo Umpierrez

Status and phase: Completed; Phase 4

Conditions: Weight Gain; Pregnancy

Treatments: Behavioral: Lifestyle Intervention group; Behavioral: Standard of Care

Study type: Interventional

Funder types: Other

Identifiers

NCT01084941

IRB00030742

Details and patient eligibility

About

The prevalence of overweight and obesity is increasing among pregnant women in the United States. More than one-third of women of reproductive age in the US are overweight or obese, and two thirds of women gain more weight in pregnancy than is recommended by the Institute of Medicine guidelines. Maternal obesity during pregnancy increases the risk of complications to both mother and child. Minority women (Blacks and Hispanics) have higher rates of overweight and obesity when they become pregnant, experience higher rates of excessive weight gain during pregnancy, and experience higher rates of maternal and neonatal complications after adjusting for sociodemographic characteristics and comorbidities than Caucasian women. Epidemiologic studies indicate that lifestyle modification programs based on diet and exercise are promising approaches in controlling weight gain as well as in preventing type 2 diabetes in populations at risk. We hypothesize that overweight/obese minority women (Blacks and Hispanics) assigned to a culturally-grounded lifestyle intervention program based on diet and moderate exercise will result in higher compliance with Institute of Medicine guidelines for weight gain than women receiving standard care. Such lifestyle modifications should reduce risk of maternal and neonatal complications. We propose 1) to determine whether a lifestyle intervention program, based on diet and moderate physical activity implemented shortly after first recognition of pregnancy, will result in higher compliance with Institute of Medicine guidelines for weight gain compared to women receiving standard care; 2) to determine the occurrence of carbohydrate intolerance and GDM at 24-28 weeks gestation (after the first 10-12 weeks of intervention) and at 6 weeks postpartum between women in the lifestyle intervention group and women receiving standard care; and 3) to explore the impact of the lifestyle intervention on the development of maternal and fetal complications during pregnancy. By limiting excessive weight gain, the lifestyle intervention program may prevent the burden of obesity-related complications during pregnancy and reduce risk of subsequently developing overt diabetes.

Enrollment: 57 patients

Sex: Female

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

---

57 participants in 2 patient groups

Lifestyle intervention

Experimental group

Description:

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.

Treatment:

Behavioral: Lifestyle Intervention group

Standard of care group

Active Comparator group

Description:

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.

Treatment:

Behavioral: Standard of Care