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Integrated Community Case Management Study in Eastern Province, Zambia

Strengthening the Delivery of Integrated Community Case Management (iCCM) in Two Districts of Eastern Province, Zambia

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02866097
Enrollment
3840
Registered
2016-08-15
Start date
2016-03-31
Completion date
2016-09-30
Last updated
2016-08-15

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

Conditions

Malaria, Diarrhea, Pneumonia

Keywords

integrated community case management, Mobile Health (mHealth), rapid diagnostic test, artemether-lumefantrine, amoxicillin, zinc, oral rehydration solution (ORS), District Health Information System 2 (DHIS2), iCCM-DHIS2, ZCAHRD

Brief summary

This study will provide important evidence to the Ministry of Community Development, Mother and Child Health (MCDMCH) and the Ministry of Health (MOH) on how to effectively implement iCCM with a focus on improving both the flow of supplies to CHWs as well as the quality of their supervision and mentorship. The overall aim will be to determine whether improvements in supplies for community health workers (CHWs) and strengthened supervision result in improved early and appropriate treatment for children with malaria, pneumonia, and diarrhea in rural Zambia when compared to CHWs offering iCCM without this logistics and supervision support.

Detailed description

The main objective of this study is to strengthen the delivery of integrated community case management (iCCM) of malaria, diarrhea, and pneumonia in Chadiza and Chipata Districts of Eastern Province, through mHealth supported improved supply chain management of iCCM commodities and enhanced supportive supervision of iCCM-trained CHWs.

Interventions

OTHERmHealth inventory management

Improved stock management of iCCM commodities using the DHIS2 mHealth platform

Strengthening of supportive supervision using DHIS2

OTHERICCM current standard of care

ICCM implementation as per current practice without mHealth interventions

Sponsors

UNICEF
CollaboratorOTHER
Bill and Melinda Gates Foundation
CollaboratorOTHER
Boston University
CollaboratorOTHER
Ministry of Health, Zambia
CollaboratorOTHER_GOV
Ministry of Community Development, Mother and Child Health
CollaboratorUNKNOWN
Zambia Center for Applied Health Research and Development
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
1 Months to 5 Years
Healthy volunteers
No

Inclusion criteria

* Age \<5 years * Treatment for an iCCM condition (malaria, pneumonia, or diarrhea) by a CHW * Willingness of the child's caregiver to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Composite percentage of children appropriately treated for malaria, diarrhea, and pneumonia.Through study completion, up to six monthsDefined as percentage of sick children under five years of age presenting with an i-CCM condition to an i-CCM trained health worker (CHW or a CHA) who received appropriate treatment for an iCCM condition (composite indicator): Appropriate treatment for malaria: received artemisinin-based combination therapy (ACT) for malaria for at least three days or Appropriate treatment for pneumonia: received amoxicillin for pneumonia for at least five days or Appropriate treatment for diarrhea: received zinc in addition to fluid from ORS packet or oral rehydration solution (ORS) liquid or homemade fluid for diarrhea

Secondary

MeasureTime frameDescription
b) Clinical supervision coverageThrough study completion, up to six monthsDefined as proportion of CHWs who received at least one supervisory contact (in person) every 3 months during which a sick child visit or scenario was assessed and coaching provided.
c) Virtual supervision coverage (via mobile technology)Through study completion, up to six monthsDefined as proportion of CHWs who received at least SMS per month from their supervisor reinforcing the appropriate use of the iCCM algorithm for classification and treatment.
d) Average cost per iCCM contactThrough study completion, up to six monthsDefined as average expenditure per iCCM contact by type of condition
a) Medicine availability (artemether-lumefantrine)Through study completion, up to six monthsDefined as percentage of iCCM sites with artemether-lumefantrine in stock during the monthly assessments
f) Medicine availability (amoxicillin)Through study completion, up to six monthsDefined as percentage of iCCM sites with amoxicillin in stock during the monthly assessments
g) Medicine availability (ORS)Through study completion, up to six monthsDefined as percentage of iCCM sites with ORS in stock during the monthly assessments
h) Medicine availability (Zinc)Through study completion, up to six monthsDefined as percentage of iCCM sites with Zinc in stock during the monthly assessments
e) Diagnostic availabilityThrough study completion, up to six monthsDefined as percentage of iCCM sites with all iCCM diagnostics (malaria rapid diagnostic tests) in stock during the monthly assessments

Countries

Zambia

Contacts

Primary ContactGodfrey Biemba, MBChB, M.Sc
biemba@bu.edu260974770293
Backup ContactBoniface M Chiluba, B.Sc, M.Sc
chiluboni@yahoo.com260977820763

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026