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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
London School of Hygiene and Tropical Medicine
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malaria focused on measuring Home-based care, Malaria, Africa

Eligibility Criteria

1 Year - 5 Years (Child)All SexesDoes not accept healthy volunteers

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

    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
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    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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