Studies have shown that overweight and obese women are at increased risk for several complications of pregnancy, including gestational diabetes mellitus, hypertension, preeclampsia, and cesarean delivery. Additionally, the children of overweight or obese pregnant women show an increased risk of prematurity, congenital anomalies, and childhood obesity. The Lifestyle Interventions for Expectant Mothers (LIFE-Moms) consortium was a network of seven clinical centers and a data coordinating center to identify effective behavioral and lifestyle interventions that improve weight, glycemic control, and outcomes in obese and overweight pregnant women and their children.
Participants were randomized between 9 weeks 0 days and 15 weeks 6 days gestation, and followed through one-year postpartum. Standardized measures were collected throughout gestation: at baseline (9-15 weeks), 24-27 weeks, 35-36 weeks, delivery, and one-year postpartum. Eligibility criteria, specific outcome measures, and assessment procedures were standardized across trials. Measures that were collected in all seven trials were defined as ‘core’ data and measures collected by four to six trials were defined as ‘super-shared’ data. All core and super-shared measures had a standardized definition and/or detailed procedures to facilitate uniform collection, a standardized training and certification process, and were entered into a common dataset at the data coordinating center.
The overall goal of the consortium was to identify effective behavioral and lifestyle interventions that would improve weight, glycemic control, and other pregnancy-related outcomes in obese and overweight pregnant women and determine whether these interventions reduced obesity and metabolic abnormalities in children.
The primary outcome measure was gestational weight gain per week, assessed by serial weight measurements up to 36 weeks gestation. Secondary outcome measures included obstetric outcomes (e.g., gestational hypertension and preeclampsia, gestational diabetes, preterm delivery), maternal one-year postpartum outcomes (e.g., postpartum weight retention), neonatal outcomes (e.g., birth weight, respiratory morbidity, hypoglycemia), and neonatal and infant anthropometrics (e.g., length, skinfold thickness). Site specific measures can be found in the LIFE-Moms Synopses document.
Core inclusion criteria:
Core exclusion criteria:
Site specific inclusion and exclusion criteria can be found in the LIFE-Moms Synopses document.
Pooled findings from the LIFE-Moms consortium found that among the randomized women, the percent with excess gestational weight gain per week as well as overall weight gain from enrollment in early pregnancy to 36 weeks gestation, was significantly lower in the intervention group compared to those in standard care. However, the women in the intervention group still exceeded the Institute of Medicine (IOM) guidelines for weight gain in pregnancy. No differences were found between the intervention and standard care groups for macrosomia, cesarean section, gestational diabetes, and small-for-gestational-age infants.
Obesity, Diabetes, Multidisciplinary Research, Nutrition
Interventional
7
Obesity Disorder, Hypertensive Disorder, Preeclampsia, Gestational Diabetes
Behavioral Therapy
None
https://clinicaltrials.gov/ct2/show/NCT01771133
https://clinicaltrials.gov/ct2/show/NCT01631747
https://clinicaltrials.gov/ct2/show/NCT01610752
http://www.clinicaltrials.gov/show/NCT01812694
https://clinicaltrials.gov/ct2/show/NCT01616147
https://clinicaltrials.gov/ct2/show/NCT01545934
https://clinicaltrials.gov/ct2/show/NCT01768793
Gestational Diabetes, Pregnancy, Hypertension, Diet Therapy, Obstetric Outcomes, Weight Control, Intensive Lifestyle Intervention, Body Mass Index (BMI), One-Year Postpartum, Gestational Weight Gain, Postpartum Outcomes, Neonatal Outcomes
Division of Digestive Diseases and Nutrition (DDN)
Use is allowed for health, medical, or biomedical research purposes
NIDDK-CR has determined that this NIDDK-funded study meets the criteria deemed to be issued a Certificate of Confidentiality. More information on what this means to Requestors is available in the NIH FAQ.
Specimen | Count |
|---|---|
| Placenta Tissue | 2750 |
| Plasma | 23263 |
| Serum | 16169 |
| Urine | 4549 |
| Whole Blood | 4991 |