Survey on maternal health and pregnancy outcomes in Zambia
Antenatal and Postnatal Care Research Collective - Household Survey (ARCH)
This study is trying to understand the health of pregnant women and their babies in Zambia by checking in with them regularly to see what affects their pregnancy outcomes.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 7500 (estimated) |
| Ages | 1 Day to 49 Years |
| Sex | All |
| Sponsor | University of North Carolina, Chapel Hill Academic / other |
| Locations | 1 site (Lusaka) |
| Trial ID | NCT05154331 on ClinicalTrials.gov |
What this trial studies
The ARCH Survey aims to establish a longitudinal study in Lusaka, Zambia, to monitor pregnancy rates and outcomes among women of reproductive age. Participants will be visited quarterly for up to three years, during which their medical records will be reviewed, physical exams conducted, and surveys administered. The study seeks to identify factors contributing to adverse pregnancy outcomes, enhancing understanding of the health needs of women and their infants. This information will ultimately inform better healthcare practices for mothers and children.
Who should consider this trial
Good fit: Ideal candidates are women of reproductive age (15-49 years) living in the catchment area who can provide informed consent.
Not a fit: Patients with conditions that may complicate participation or data interpretation may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved maternal and infant health care practices in Zambia.
How similar studies have performed: Other studies focusing on maternal health in similar contexts have shown success in identifying key health determinants and improving outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
We will initially obtain verbal consent from the head of household (HoH), defined as an available adult (\> 18 years old) who is able to provide information about household composition for pre-screening purposes. We will then identify potentially eligible women of reproductive age within each household and invite them to complete study screening procedures. Women of reproductive age eligibility criteria Inclusion criteria: * Verbal consent obtained from head-of-household * 15-49 years of age and a member of household in the catchment area * Willing and able to provide written informed consent or assent with next-of-kin consent * Willing to undergo study procedures Exclusion criteria: Any other condition (social or medical) that, in the opinion of the study staff, would make participation unsafe or complicate data interpretation. Study staff may note physical, psychological, or social conditions not explicitly stated in the eligibility criteria that could make some women poor candidates for study participation.
Where this trial is running
Lusaka
- University of Zambia — Lusaka, Zambia (Recruiting)
Study contacts
- Principal investigator: Jeff Stringer — University of North Carolina, Chapel Hill
- Study coordinator: Mutale Sampa
- Email: mutalesampa65@gmail.com
- Phone: +260977287091
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.