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Buikwe Electronic Community Health Information System Impact Study

A Research Study to Understand the Impact and Cost-effectiveness of a Digital Health Platform for iCCM in Uganda

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06318078
Enrollment
1140
Registered
2024-03-19
Start date
2023-12-01
Completion date
2024-07-31
Last updated
2024-03-19

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

Conditions

Diarrhea, Malaria, Pneumonia

Brief summary

The purpose of the study is to investigate the impact of the eCHIS intervention on key child health outcomes.

Detailed description

Following national guidelines, 2 VHTs per village will be supported to provide the full eCHIS community health package. In total 856 VHTs in Buikwe district will have been trained and equipped with the national strategy and operational guidelines on eCHIS as well as the VHT full package (iCCM+ and VHT basic package (reproductive health, immunization, nutrition) guidelines. The VHTs will be equipped with mobile devices and iCCM supplies to start the management of community-based health among children aged five years within their respective communities. A cross-sectional cluster randomized controlled trial (cRCT) will be used to establish study outcomes in children under 5 years in the intervention and control areas using mixed methods (qualitative and quantitative) of data collection. A total sample size of 1,140 children under five: 570 children under five, per arm, was scientifically determined for the study. During data collection, several quality control measures will be applied to ensure the data recorded reflect the facts, responses, observations, and events. A standard operating procedure (SOP) with roles and responsibilities of the data collectors will be prepared to ensure standardized methods for capturing data. After endline data collection, difference-in-differences (DID) analysis will be done to derive an estimate of the intervention effect on odds of the study outcomes. Results will be disseminated through agreed peer-review publications and international conferences. Malaria Consortium Uganda will work with relevant stakeholders at the Ministry of Health and Medic Mobile to disseminate findings nationally and throughout the study district.

Interventions

OTHEReCHIS

The electronic Community health Information System (eCHIS) is a Government of Uganda owned application used by community health workers for quality health assessments and improved reporting. The eCHIS intervention allows for the registration of longitudinal profiles for client centered care as well as provides care guidance to aid decision making. For its users, the app has a task tab for schedule management and dashboards for performance help management and impact tracking by supervisors. This app is interoperable with national reporting tools such as DHIS2. The app has ten workflows including registration of households and new persons, death reporting, iCCM assessment, treatment and referral follow up, stock monitoring, data synchronization, pregnancy registration, ANC danger signs and follow up, family planning registration, and screening (tuberculosis, hypertension, sickle cell, tobacco use and net use).

Sponsors

Malaria Consortium
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Cluster Randomised Control Trial

Eligibility

Sex/Gender
ALL
Age
3 Months to 59 Months
Healthy volunteers
No

Inclusion criteria

* · Children between 3-59 months, * Being resident in the study area, * Consent to participate in the study obtained, * Willingness and ability of the child's guardians to comply with the study protocol for the duration of the study including attending a designated health centre if their child has malaria symptoms during the data collection period.

Exclusion criteria

* Children aged below 3 months and above 59 months * Children resident outside the study areas * Those who have not consented to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
Out Patient Department attendance (due to malaria, pneumonia and diarrhoea)Over 1 yearAttendance measured through baseline and endline surveys
Hospitalisation (due to malaria, pneumonia and diarrhoea)Over 1 yearAttendance measured through baseline and endline surveys
malaria related mortality in the community and health facilitiesOver 1 yearMalaria related mortality measured through routine data

Countries

Uganda

Contacts

Primary ContactJohn Baptist Bwanika
j.bwanika@malariaconsortium.org+256 772744390
Backup ContactKevin Baker
k.baker@malariaconsortium.org07811266539044

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026