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Effect of Physical Activity on Metabolic Syndrome in Pregnancy & Fetal Outcome

Phase 3
Completed
Conditions
Obesity
Pregnancy
Diabetes Mellitus
Interventions
Behavioral: Experimental group
Registration Number
NCT00647595
Lead Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Brief Summary

The purpose of this study is to examine the effect of exercise during pregnancy upon maternal metabolism, including weight gain, fat distribution, and levels of glucose and cholesterol. We will also conduct a pilot study to examine the feasibility of studying the health of infants born to women in this study.

Detailed Description

Obesity and overweight have become important public health problems in the United States, and measures are urgently needed to address these issues. For many women, pregnancy is a time of excessive weight gain and decreases in physical fitness, both of which may be followed by postpartum weight retention. Women who develop hypertension or diabetes mellitus during pregnancy are at higher risk for development of these disorders in the future. Because of the implications of pregnancy-related weight gain and the metabolic changes during pregnancy for future maternal health, interventions to maintain or improve fitness during pregnancy may have important downstream health effects. In addition, maternal metabolic parameters and the intra-uterine environment have important implications for neonatal outcomes and subsequent child health. This study will provide data about the effects of an intervention to increase vigorous physical activity during pregnancy on short-term maternal and fetal outcomes.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
100
Inclusion Criteria
  • Pregnant women 18-45 years old receiving prenatal care at MAMC
Exclusion Criteria
  • Women do not have a gallbladder
  • Who do not speak English
  • Are over 14 weeks pregnant at study entry
  • Do not plan to deliver at MAMC
  • Have medical contraindications
  • Unwilling to participate in exercise intervention program
  • Are under 18 years of age
  • Currently engaged in a regular vigorous exercise program

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
AExperimental groupWomen in this group will exercise 3x per week at a moderate/vigorous level for 45 min per session through their 36 week of pregnancy.
Primary Outcome Measures
NameTimeMethod
Central adiposity6-8 weeks postpartum
Secondary Outcome Measures
NameTimeMethod
neonatal adipositybirth
Leptin levelsduring pregnancy and postpartum
glucoseduring pregnancy and postpartum
insulinduring pregnancy and postpartum
cholesterolduring pregnancy and postpartum
fetal adiposity35-36 weeks gestation

Trial Locations

Locations (1)

Madigan Army Medical Center

🇺🇸

Ft Lewis, Washington, United States

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