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Enhancing Universal Health Coverage and Maternal, Newborn and Child Health in Kenya Through Digital Innovations

Innovative Partnership for Universal Health Coverage

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04068571
Acronym
UHC
Enrollment
300
Registered
2019-08-28
Start date
2019-09-30
Completion date
2020-04-30
Last updated
2019-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Universal Health Coverage

Brief summary

This study aims at providing insights into Universal Health Coverage and evaluates the impact of I-PUSH program on maternal healthcare utilization, financial protection and women's empowerment, as well as to evaluate the impact of the LEAP training tool on community health volunteers and women's health literacy including their knowledge, behavior and uptake of respective services.

Detailed description

The study will use a three-pronged approach: year-long weekly Financial and Health Diaries, Baseline and Endline surveys, and qualitative interviews. The Diaries and the Surveys will be carried out in two Counties, Kakamega and Kisumu (Kenya). The qualitative interviews will be carried out in the two counties and in Nairobi as an additional county. The study will use a cluster randomized control trial design in Kakamega to evaluate the impact of I-PUSH program. In Kisumu, selected households will be followed-up to capture the health-seeking behavior, health insurance, and health expenditure pattern of households over time. The study will be initially for 17 months and will continue for three years subject to additional funding.

Interventions

BEHAVIORALI-PUSH

Innovative partnership for universal and sustainable healthcare

Sponsors

Amsterdam Institute for Global Health and Development
CollaboratorOTHER
PharmAccess
CollaboratorUNKNOWN
African Population and Health Research Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
15 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Targets for the intervention

Exclusion criteria

* Non-targets for the intervention

Design outcomes

Primary

MeasureTime frameDescription
Health Care Utilization17 monthsFinancial and health diaries will be collected on a weekly basis throughout the indicated study period
Maternal, Newborn and Child Health outcomes through out the continuum of care17 monthsQuestionnaire based survey questions will be used to measure these outcomes

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026