Evaluation of Home-Based Management of Fever in Urban Ugandan Children
Primary Purpose
Malaria, Anemia
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Provision of antimalarial treatment at home
Sponsored by
About this trial
This is an interventional treatment trial for Malaria focused on measuring Home-based care, Malaria, Africa
Eligibility Criteria
Inclusion Criteria: Age 1 - 5 years Agreement of parents or guardians to provide informed consent Live in Mulago III Parish Exclusion Criteria: History of any known serious chronic disease requiring frequent medical care (e.g. AIDS, sickle cell disease, malignancy) Intention to move from Kampala during the 13 month follow-up period History of serious side effects to study medications Weight < 10 kg Severe malnutrition defined as a weight-for-height or height-for-age Z-score < - 3
Sites / Locations
Outcomes
Primary Outcome Measures
The primary outcome measurement will be treatment incidence density (antimalarial treatments received per time at risk) for each study arm.
Secondary Outcome Measures
Mean days of fever per participant
Incidence of febrile episodes
Mean haemoglobin at study end
Change in mean haemoglobin between the start and end of the intervention
Incidence of visits to health care facilities (drug shops, clinics, pharmacies, hospitals) and hospitalizations per participant
Mortality rate
Economic outcomes
Full Information
NCT ID
NCT00115921
First Posted
June 26, 2005
Last Updated
January 11, 2017
Sponsor
London School of Hygiene and Tropical Medicine
Collaborators
Makerere University, University of California, San Francisco
1. Study Identification
Unique Protocol Identification Number
NCT00115921
Brief Title
Evaluation of Home-Based Management of Fever in Urban Ugandan Children
Official Title
Evaluation of Home-Based Management of Fever in Urban Ugandan Children
Study Type
Interventional
2. Study Status
Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
July 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
April 2007 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
London School of Hygiene and Tropical Medicine
Collaborators
Makerere University, University of California, San Francisco
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to see if providing effective antimalarial treatment at home for parents/guardians to treat their children for malaria will lead to an improved health outcome compared to conventional healthcare.
Detailed Description
Population: Representative sample of Ugandan children aged 1 to 5 years from 400 households (approximately 540 children).
Clinical Site: The study will be conducted in the Mulago III parish community of Kampala, Uganda.
Study Duration: 13 months
Study Intervention: *Pilot period: After enrollment, households will participate in a one month pilot period to test the household pictorial diaries. At the end of the pilot period, households will be randomized to participation in the home-based management of fever (HBMF) arm or standard care arm for the remainder of the study (12 months). *HBMF arm: Households randomized to the HBMF group will be provided with pre-packaged coartemether to keep at home. Primary caregivers will be instructed to treat children participating in the study empirically with coartemether at home when the child develops fever. Study personnel will distribute drugs and educate the caregivers about administration of drugs, recognition of danger signs of fever/malaria, and when to seek additional care. *Standard care: Households randomized to the standard care arm will be asked to continue their current behaviour and to manage fever in their children as they would normally.
Measurements: Household diaries and monthly visits. Primary caregivers will be asked to keep a diary regarding the health of study participants for the duration of the study (13 months). Information on illnesses, treatments given, visits to health care facilities, and health care expenditures will be collected. Study personnel will visit the households monthly to collect completed diaries. At each visit, questionnaires will be administered to gather additional data on the health of the participants and treatment seeking behaviour.
Clinical and laboratory evaluations: Temperature, height, weight, mid-upper arm circumference, spleen size, haemoglobin, and thick blood smear will be assessed at enrollment, and at the beginning and end of the intervention period.
Study Objectives: 1. To measure the impact of home-based management of fever with coartemether on malaria-related morbidity compared to the current standard of care in the community.
2. To measure the impact of home-based management of fever with coartemether on economic measures compared to the current standard of care in the community.
Primary outcome: Treatment incidence density (treatments per time at risk) for each treatment arm
Secondary clinical outcomes: 1) mean days of fever; 2) incidence of febrile episodes; 3) mean haemoglobin at study end; 4) change in mean haemoglobin; 5) prevalence of splenomegaly; 6) prevalence of parasitaemia; 7) incidence of visits to health care facilities, and hospitalizations; 8) mortality rate; 9) anthropometric measurements; 10) proportion of "appropriate" treatments; 11) proportion of delayed treatments; 12) treatment incidence density of treatments given at >50% and at full dose
Economic outcomes: 1) household cost/febrile episode; 2) household costs for treatment of febrile episode/month; 3) provider cost/child for delivery of HBMF; 4) estimated provider facility cost/patient for uncomplicated fever, and for severe disease; 5) total net cost/child/year; 6) net cost/additional child appropriately treated; 7) net cost/day of fever averted
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malaria, Anemia
Keywords
Home-based care, Malaria, Africa
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
540 (false)
8. Arms, Groups, and Interventions
Intervention Type
Behavioral
Intervention Name(s)
Provision of antimalarial treatment at home
Primary Outcome Measure Information:
Title
The primary outcome measurement will be treatment incidence density (antimalarial treatments received per time at risk) for each study arm.
Secondary Outcome Measure Information:
Title
Mean days of fever per participant
Title
Incidence of febrile episodes
Title
Mean haemoglobin at study end
Title
Change in mean haemoglobin between the start and end of the intervention
Title
Incidence of visits to health care facilities (drug shops, clinics, pharmacies, hospitals) and hospitalizations per participant
Title
Mortality rate
Title
Economic outcomes
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 1 - 5 years
Agreement of parents or guardians to provide informed consent
Live in Mulago III Parish
Exclusion Criteria:
History of any known serious chronic disease requiring frequent medical care (e.g. AIDS, sickle cell disease, malignancy)
Intention to move from Kampala during the 13 month follow-up period
History of serious side effects to study medications
Weight < 10 kg
Severe malnutrition defined as a weight-for-height or height-for-age Z-score < - 3
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sarah G Staedke, MD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Christopher JM Whitty, FRCP
Organizational Affiliation
London School of Hygiene and Tropical Medicine
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
PubMed Identifier
19362361
Citation
Staedke SG, Mwebaza N, Kamya MR, Clark TD, Dorsey G, Rosenthal PJ, Whitty CJ. Home management of malaria with artemether-lumefantrine compared with standard care in urban Ugandan children: a randomised controlled trial. Lancet. 2009 May 9;373(9675):1623-31. doi: 10.1016/S0140-6736(09)60328-7. Epub 2009 Apr 9.
Results Reference
derived
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Evaluation of Home-Based Management of Fever in Urban Ugandan Children
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