Evaluation of Electronic Pregnancy Registers and Mobile Applications for Monitoring Pregnancy Outcomes ( EVAPREAP )

NCT06225739 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2000

Last updated 2025-08-05

No results posted yet for this study

Summary

Monitoring pregnancy outcomes during pregnancy is very important in assessing the effectiveness of interventions. This study aims to create pregnancy registers and evaluate pregnancy mobile applications as a potential tool for monitoring pregnancy outcomes in future placental malaria (PM) vaccine trials, as well as for the implementation of any other intervention in this target group.

Conditions

  • Pregnancy Related

Interventions

OTHER

Electronic pregnancy register

Electronic pregnancy register will be created based on local ANC register to monitor pregnancy outcomes across all sites. Pregnant women of all ages attending antenatal care (ANC) facility will be registered

OTHER

In-depth interviews and focus group discussions

In-depth interviews (IDIs) and focus group discussions (FGDs) will be used to assess the user experience and the perceptions of pregnant women and health workers on the feasibility, usability, and acceptability of open-source mobile applications for tracking pregnancy outcomes

Sponsors & Collaborators

  • Kintampo Health Research Centre, Ghana

    collaborator OTHER
  • Fondation pour la Recherche Scientifique, Benin

    collaborator UNKNOWN
  • Groupe de Recherche Action en Sante

    collaborator OTHER
  • Malawi University of Science and Technology

    collaborator UNKNOWN
  • European Vaccine Initiative

    lead OTHER

Principal Investigators

  • Kwaku Poku Asante, MD, PhD · Kintampo Health Research Centre, Ghana

Eligibility

Min Age
15 Years
Max Age
49 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-10-01
Primary Completion
2025-04-30
Completion
2025-04-30

Countries

  • Benin
  • Burkina Faso
  • Ghana
  • Malawi

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06225739 on ClinicalTrials.gov