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Home Management of Malaria and Pneumonia

Home and Community Management of Fevers/Malaria and Pneumonia in Children Under-five: a Cluster Randomised Controlled Trial of an Integrated Approach in a Rural District of Burkina Faso

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02151578
Acronym
HMM/P
Enrollment
11500
Registered
2014-05-30
Start date
2009-01-31
Completion date
2012-09-30
Last updated
2014-05-30

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

Conditions

Malaria, Pneumonia

Keywords

Impact of home management of malaria and pneumonia on child mortality, home management of malaria and pneumonia

Brief summary

A well-implemented community-based program of early and appropriate treatment of fevers/malaria episodes and pneumonia,will improve child survival as measured by a reduction of the less than five mortality rate.

Detailed description

An integrated approach of home and community management of malaria and pneumonia may increase the proportion of children receiving prompt treatment; improve child survival as measured by a reduction of the under five mortality rate. To test this hypothesis, a cluster randomised controlled trial will be performed, involving children less than 5 years of age, in Burkina Faso using a community-based supplying community health workers (CHWs), a core group of mothers (KOLs) with Coartem and cotrimoxazole specially packed in age-specific blisters containing a full course of treatment. The study will be carried out in 111 clusters of a rural district in Burkina Faso where malaria and pneumonia are two major mortality causes in under five mortality.

Interventions

OTHERhome/community case management

Sponsors

World Health Organization
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* living in one of the study cluster (villages) * no story of allergy to any of the study drugs * history of fever or body temperature \>= 38.5°C

Exclusion criteria

* signs of severity/complications like impaired consciousness, convulsions, fast breathing etc

Design outcomes

Primary

MeasureTime frameDescription
Number of death in children aged 6 to 59 months12 monthsannual crude mortality rate in children aged 0 to 6 months in the different study arms

Secondary

MeasureTime frame
- specific mortality preceded by acute febrile illness of children aged 6 to 59 months - severe malaria cases at community level12 months

Other

MeasureTime frame
Adverse events at community level consecutive to the administration of the cotrimoxazole and arthemeter/lumefantrine7 days after the administration of the drug

Countries

Burkina Faso

Outcome results

None listed

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