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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02072629
Other study ID # E-22746
Secondary ID
Status Completed
Phase N/A
First received February 21, 2014
Last updated February 25, 2014
Start date November 2009
Est. completion date December 2012

Study information

Verified date February 2014
Source University of Calgary
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Interventional

Clinical Trial Summary

This study will assess how the current VHV (VHV=CHW, community health worker) scope can be expanded to include iCCM and if such group interventions can provide improved access to treatment for children.

In rural SW Uganda, can iCCM provided by lay volunteers, increase the proportion of children with diarrhoea receiving ORS/Zn, ARI receiving anti-biotics, and fever/malaria receiving anti-malarials?


Recruitment information / eligibility

Status Completed
Enrollment 4071
Est. completion date December 2012
Est. primary completion date December 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Women living in intervention and comparison villages

- Mother to at least one child under 59 months old

Exclusion Criteria:

-No living child

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Other:
Training of VHVs in iCCM
Village Health Volunteers will be trained in Integrated Community Case Management (iCCM) of childhood illness

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
University of Calgary Mbarara University of Science and Technology

Outcome

Type Measure Description Time frame Safety issue
Primary Absolute change pre/post intervention (VHV ICCM training) in proportion of U5s receiving (a) antimalarial for fever (b) ORS/Zn for diarrhea (c) Abx for pneumonia pre- (Dec 2010) post- (Dec 2012) intervention (2 years) No
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