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Assessment of Use of Rapid Diagnostic Testing in the Context of Home Management With ACTs

Primary Purpose

Malaria, Pneumonia

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Artemether-lumefantrine combination
amoxycillin
paracetamol
malaria rapid diagnostic test, respiratory rate timer
Artemether-lumefantrine combination
Sponsored by
Mbarara University of Science and Technology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malaria focused on measuring Malaria ACT, Rapid, Diagnosis, Community, health, worker, Artemesinin, based, Combination, Therapy, Anti Malarial, Treatment, antibiotics

Eligibility Criteria

4 Months - 59 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children between 4-59 months of age with a history of fever in the last 24 hours presenting to the community medicine distributor

Exclusion Criteria:

  • Children classified as having severe illness according to IMCI guidelines. Children suffering from Chronic disease(s), those with reported anti malarial or antibiotic treatment (intervention) arm in previous two weeks and those whose caregivers refuse to consent to participate

Sites / Locations

  • Sapone Site
  • Kassena Nankana Site
  • Iganga Site
  • Mbarara Site

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

ACT, antibiotic, paracetamol

Presumptive fever management

Arm Description

CHWs will test children with acute febrile illness for malaria using RDTs, and for pneumonia by counting their respiratory rate with RRTs. Treatment will then be provided on the basis of the test results, in line with national guidelines. Children with a positive RDT will receive artemether-lumefantrine in Burkina Faso and Uganda, and artesunate-amodiaquine in Ghana. Children with a cough and a high respiratory rate will receive amoxicillin in Ghana and Uganda, and cotrimoxazole in Burkina Faso. Additionally, paracetamol (PCT) will be provided to all children with an axillary temperature > 38.5°C.

Presumptive treatment of malaria with ACTs. No antibiotic treatment available

Outcomes

Primary Outcome Measures

Recovery rate from fever at Day 3

Secondary Outcome Measures

use of antimalarial and antibiotic drugs by community health workers
Recovery rate from fever at Day 7

Full Information

First Posted
July 21, 2008
Last Updated
March 15, 2012
Sponsor
Mbarara University of Science and Technology
Collaborators
Makerere University, Ministry of Health, Uganda, Navrongo Health Research Centre, Ghana, National Malaria Research and Training Centre, Burkina Faso
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1. Study Identification

Unique Protocol Identification Number
NCT00720811
Brief Title
Assessment of Use of Rapid Diagnostic Testing in the Context of Home Management With ACTs
Official Title
Assessment of Use of Rapid Diagnostic Testing in the Context of Home Management With ACTs
Study Type
Interventional

2. Study Status

Record Verification Date
March 2012
Overall Recruitment Status
Completed
Study Start Date
October 2009 (undefined)
Primary Completion Date
January 2012 (Actual)
Study Completion Date
January 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Mbarara University of Science and Technology
Collaborators
Makerere University, Ministry of Health, Uganda, Navrongo Health Research Centre, Ghana, National Malaria Research and Training Centre, Burkina Faso

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study is to assess the value of incorporating a malaria RDT based strategy in HMM. The primary activity of the study wil be a two armed cluster randomised trial in two study sites in Uganda, one in Ghana and one in Burkina Faso. One of the Uganda sites is highly endemic and the other meso-endemic for malaria. In one arm the children will be treated presumptively for malaria with ACT (control arm) and the other arm the children will receive ACT only when they have a positive RDT result (implementation arm). The children in the implementation arm will also receive antibiotics if they have a raised respiratory rate. The primary outcome will be the recovery rate in the intervention arm compared to that of the control arm on Day 3. In addition, an acceptability assessment of RDTs in the community will be undertaken both before and after the intervention trial and a cost-effectiveness analysis of the RDT strategy will also be completed. For a sub-sample, microscopy slides will also be taken on Day 0 to demonstrate comparable levels of endemicity in control and intervention groups. These activities will be carried out over a two year period.
Detailed Description
This is an open, cluster randomised multicentre two arm trial in the three countries of Burkina Faso, Ghana and Uganda. Clusters are villages (catchment populations) of individual community health workers (CHWs). Within the study areas, clusters that are more than 5 km from a designate health facility where CHWs referred cases for special care will be excluded. A cluster randomized design was chosen over an individually randomized design to reduce contamination, facilitate supervision, reduce costs, and to ensure that the CHWs maintained the correct treatments based on the tests in the Intervention arm and the presumptive treatment in the Control arm.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malaria, Pneumonia
Keywords
Malaria ACT, Rapid, Diagnosis, Community, health, worker, Artemesinin, based, Combination, Therapy, Anti Malarial, Treatment, antibiotics

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
6456 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ACT, antibiotic, paracetamol
Arm Type
Experimental
Arm Description
CHWs will test children with acute febrile illness for malaria using RDTs, and for pneumonia by counting their respiratory rate with RRTs. Treatment will then be provided on the basis of the test results, in line with national guidelines. Children with a positive RDT will receive artemether-lumefantrine in Burkina Faso and Uganda, and artesunate-amodiaquine in Ghana. Children with a cough and a high respiratory rate will receive amoxicillin in Ghana and Uganda, and cotrimoxazole in Burkina Faso. Additionally, paracetamol (PCT) will be provided to all children with an axillary temperature > 38.5°C.
Arm Title
Presumptive fever management
Arm Type
No Intervention
Arm Description
Presumptive treatment of malaria with ACTs. No antibiotic treatment available
Intervention Type
Drug
Intervention Name(s)
Artemether-lumefantrine combination
Other Intervention Name(s)
Coartem
Intervention Description
20/120mg Artemether-lumefantrine 4-35 months: 1 tablet twice daily for 3 days; 36-59 months: 2 tablets twice daily for 3 days
Intervention Type
Drug
Intervention Name(s)
amoxycillin
Intervention Description
amoxycillin 250mg tab 4-12 months: 1/2x2; 13-35 months: 1x2; 36-59 months: 11/2x2
Intervention Type
Drug
Intervention Name(s)
paracetamol
Intervention Description
paracetamol 500mg tablet <36months: 1/4x4 for 2 days; 36-59months: 1/2x4 for 2 days
Intervention Type
Device
Intervention Name(s)
malaria rapid diagnostic test, respiratory rate timer
Intervention Description
malaria dipstick, and breath timer
Intervention Type
Drug
Intervention Name(s)
Artemether-lumefantrine combination
Intervention Description
20/120mg tablet arthermether-lumefantrine 4-35months: 1x2; 36-59months: 2x2
Primary Outcome Measure Information:
Title
Recovery rate from fever at Day 3
Time Frame
Day 3
Secondary Outcome Measure Information:
Title
use of antimalarial and antibiotic drugs by community health workers
Time Frame
After patient enrollment
Title
Recovery rate from fever at Day 7
Time Frame
Day 7

10. Eligibility

Sex
All
Minimum Age & Unit of Time
4 Months
Maximum Age & Unit of Time
59 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children between 4-59 months of age with a history of fever in the last 24 hours presenting to the community medicine distributor Exclusion Criteria: Children classified as having severe illness according to IMCI guidelines. Children suffering from Chronic disease(s), those with reported anti malarial or antibiotic treatment (intervention) arm in previous two weeks and those whose caregivers refuse to consent to participate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francis Bajunirwe, MBChB PhD
Organizational Affiliation
Mbarara University of Science and Technology
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
George Pariyo, MB ChB, PhD
Organizational Affiliation
Makerere University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
James Tibenderana, MB ChB, PhD
Organizational Affiliation
Malaria Consortium
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Alfred Tiono, PhD
Organizational Affiliation
National Malaria Research and Training Center, Burkina Faso
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Thomas Anyorigiya, MSc
Organizational Affiliation
Navrongo Health Research Centre, Ghana
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sapone Site
City
Sapone
Country
Burkina Faso
Facility Name
Kassena Nankana Site
City
Kassana
Country
Ghana
Facility Name
Iganga Site
City
Iganga
Country
Uganda
Facility Name
Mbarara Site
City
Mbarara
Country
Uganda

12. IPD Sharing Statement

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Assessment of Use of Rapid Diagnostic Testing in the Context of Home Management With ACTs

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