Abnormal postnatal glucose metabolism in pregnant women with gestational diabetes mellitus (including type 2 diabetes, impaired fasting glucose and impaired glucose tolerance)
Conditions
Interventions
Regular Care Group (RCT):Accept traditional standard postpartum management measures.
Enhanced Lifestyle Intervention Group (RCT):Implementing a joint online and offline management plan of "hospital community family" using information systems
Postpartum glucose metabolism abnormalities group (prospective cohort):None
Postpartum normal glucose metabolism group (prospective cohort):None
Sponsors
Beijing Obstetrics and Gynecology Hospital, Capital Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 44 Years
Inclusion criteria
Inclusion criteria: 1: Prospective cohort: Age range from 18 to 44 years old; GDM pregnant women who undergo regular prenatal examinations and delivery in the hospital; Singleton pregnancy. 2: RCT: Age range from 18 to 44 years old; GDM pregnant women who undergo regular prenatal examinations and delivery in the hospital; Singleton pregnancy.
Exclusion criteria
Exclusion criteria: 1: Prospective cohort: Multiple pregnancies; History of hepatitis, nephritis, digestive tract diseases (chronic gastritis, enteritis, gastric ulcer, duodenal ulcer, etc.) and infectious diseases (hepatitis, tuberculosis, etc.); Metabolic diseases (diabetes, hyperlipidemia, thyroid diseases, etc.) before pregnancy; Mental diseases; Structural abnormalities of newborns; Fetal/newborn chromosome or genome abnormalities; Incomplete clinical data; Individuals who refuse to participate in the study or are unable to follow the study plan for follow-up visits will not be included in this study. 2: RCT: Multiple pregnancies; History of hepatitis, nephritis, digestive tract diseases (chronic gastritis, enteritis, gastric ulcer, duodenal ulcer, etc.) and infectious diseases (tuberculosis, etc.); Metabolic diseases (diabetes, thyroid diseases, etc.) before pregnancy; Mental illnesses; Incomplete clinical data; Individuals who are unable or unwilling to participate in intervention and follow-up, as well as those who are not suitable for exercise, are not included in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 75g oral glucose tolerance test (OGTT);low-dentisty lipoprotein cholesteral; | — |
Secondary
| Measure | Time frame |
|---|---|
| fasting insulin;cholesteral;triglyceride;high-dentisty lipoprotein cholesteral; | — |
Countries
China
Contacts
Public ContactLi Guanghui
Beijing Obstetrics and Gynecology Hospital, Capital Medical University
Outcome results
None listed