Image

Antenatal and Postnatal Care Research Collective - Household Survey (ARCH)

Antenatal and Postnatal Care Research Collective - Household Survey (ARCH)

Recruiting
1-49 years
All
Phase N/A

Powered by AI

Overview

The overarching goal of the ARCH Survey is to establish a prospective longitudinal pregnancy surveillance study in Lusaka, Zambia, to precisely characterize the pregnancy rate and outcomes of women of reproductive age prior to, during, and following pregnancy and to investigate the structural, sociodemographic, and clinical covariates that contribute to adverse outcomes in each reproductive epoch.

Description

The overall purpose of this study is to better understand the health and well-being of women before and after they become pregnant and of their infants. This information will contribute to the understanding of the health needs of women and their children, which may help doctors provide mothers and children with better care in the future.

Participants in this study will be visited four times a year (every 3 months) for up to three years in total. At each visit a review of their medical records, a brief physical exam and urine pregnancy test will be conducted. Participants will also answer survey questions and self-collect vaginal swabs for future testing. We will enroll up to 5,500 women and include any infants that are born to them during their study participation.

Eligibility

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.

Study details
    Maternal Health
    Pregnancy Outcomes

NCT05154331

University of North Carolina, Chapel Hill

16 April 2024

Step 1 Get in touch with the nearest study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

  Other languages supported:

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.