Actively Recruiting

Phase Not Applicable
FEMALE
Healthy Volunteers
NCT05929586

Digital Data Linkage and Scheduling to Track Pregnancy With or Without Community Data Use to Increase Antenatal Clinic Uptake in Western Kenya.

Led by Liverpool School of Tropical Medicine · Updated on 2025-06-27

1440

Participants Needed

1

Research Sites

95 weeks

Total Duration

On this page

Sponsors

L

Liverpool School of Tropical Medicine

Lead Sponsor

K

Kenya Medical Research Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

The investigators propose to increase ANC uptake through a health systems strengthening approach that links digital data platforms and trains community Work Improvement Teams (WITs) to use these data to identify problems and come up with local solutions. Our short name C-it DU-it (pronounced "see-it; do-it") is an acronym intended to convey 'seeing' linked data (C-it) and 'doing' or acting on the data (DU-it). The trial design is a 2-arm, cluster-randomised controlled superiority trial in Homa Bay County to determine the efficacy of 'C-it DU-it' intervention (data use arm) to increase ANC contacts when compared to the 'C-it' enhanced standard of care (control arm).

CONDITIONS

Official Title

Digital Data Linkage and Scheduling to Track Pregnancy With or Without Community Data Use to Increase Antenatal Clinic Uptake in Western Kenya.

Who Can Participate

FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant women of all ages willing to participate
  • Written informed consent
  • Resident of the study area for the duration of the pregnancy
  • Delivered and still within the 6-week post-partum period
Not Eligible

You will not qualify if you...

  • Currently enrolled in another interventional study targeting pregnant women
  • Outside the 6-week post-partum period

AI-Screening

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Trial Site Locations

Total: 1 location

1

KEMRI Centre for Global Health Research

Homa Bay, Kenya

Actively Recruiting

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Research Team

H

Hellen C Barsosio, MD

CONTACT

L

Lilian Otiso, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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