None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: A pregnant woman who meets the following inclusion criteria may be enrolled in the study: 1. Lives within the study catchment area; 2. Meets minimum age requirement (greater than equal to 18 years) 3. Intrauterine pregnancy less than 14 weeks gestation verified via ultrasound; 4. Provides informed consent
Exclusion criteria
Exclusion criteria: Among women screened for the study, the following are exclusion criteria: 1. Nonviable (e.g. ectopic or molar) pregnancy; 2. Plans to relocate outside of the study catchment area during pregnancy and/or postpartum
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Maternal health outcomes: 1. Composite severe maternal health outcomes 2. Perinatal depression 3. Postpartum anemia through 42 days postpartum Fetal and neonatal health outcomes: 1. Preterm birth 2. Small-for-gestational age 3. Stillbirth 4. Neonatal mortalityTimepoint: During pregnancy, at delivery point and up to 42 days post-delivery At the time of delivery or up to 28 days of birth | — |
Secondary
| Measure | Time frame |
|---|---|
| Maternal health outcomes: 1. Maternal mortality, defined as a womanââ?¬â?¢s death during pregnancy and childbirth or within 42 days of termination of pregnancy 2. Late maternal mortality (up to one year post-delivery) 3. Preeclampsia/ eclampsia 4. Postpartum hemorrhage 5. Preterm premature rupture of membranes 6. Maternal sepsis 7. Maternal fatigue Timepoint: During pregnancy, at delivery point and up to one-year post-delivery;Fetal and neonatal health outcomes: 1. Low birthweight 2. Hyperbilirubinemia 3. Neonatal sepsis 4. Possible severe bacterial infection 5. Infant neurodevelopment Timepoint: At the time of delivery or up to 6 weeks of birth | — |
Countries
India
Contacts
Centre for Health Research and Development, Society for Applied Studies