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P. Falciparum Infection Dynamics and Transmission to Inform Elimination (INDIE-1a)

Not Applicable
Completed
Conditions
Malaria
Interventions
Other: Enhanced Community Case Management (CCM)
Other: Monthly Screening and Treatment (MSAT)
Registration Number
NCT03705624
Lead Sponsor
London School of Hygiene and Tropical Medicine
Brief Summary

In the current randomized trial, the investigators will test the ability of two experimental approaches to malaria infection management to reduce malaria transmission potential. Compounds in Saponé, Burkina Faso, will be randomized to 1 of 3 study arms: arm 1 - current standard of care with passively monitored malaria infections; arm 2 - standard of care plus enhanced community case management (CCM), comprising active weekly screening for fever, and detection and treatment of infections in fever positive individuals using conventional rapid diagnostic tests (RDTs); or arm 3 - standard of care and enhanced CCM, plus monthly screening and treatment (MSAT) using RDTs. The study will be conducted over approximately 18 months covering two high transmission seasons and the intervening dry season

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
907
Inclusion Criteria
  1. Participants should be permanent residents of the compound
  2. Participants should be willing to participate in repeated assessments of health and infection status and willing to donate a maximum of 37mL of blood (children <10 years of age) or 52mL of blood (older individuals) during an 18-month period
Exclusion Criteria
  1. Any (chronic) illness that would affect with study participation
  2. Pre-existing severe chronic health conditions
  3. Current participation in malaria vaccine trials or participation in such trials in the last 2 years
  4. History of intolerance to artemether-lumefantrine

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
CCMEnhanced Community Case Management (CCM)Standard of care supplemented with enhanced Community Case Management for malaria (CCM) involving weekly active screening for fever using a research-grade thermometer by a trained health worker. A measured temperature ≥37.5°C or reported fever in the last 24 hours will prompt screening with a conventional rapid diagnostic test (RDT). RDT positive individuals will be treated with artemether-lumefantrine (AL) according to national guidelines
CCM+MSATEnhanced Community Case Management (CCM)Standard of Care supplemented with CCM and Monthly Screening and Treatment (MSAT) regardless of symptoms with a conventional RDT. Screening will be performed by research staff with 25-35 days between screening rounds; RDT positive individuals will be treated with AL according to national guidelines.
CCM+MSATMonthly Screening and Treatment (MSAT)Standard of Care supplemented with CCM and Monthly Screening and Treatment (MSAT) regardless of symptoms with a conventional RDT. Screening will be performed by research staff with 25-35 days between screening rounds; RDT positive individuals will be treated with AL according to national guidelines.
Primary Outcome Measures
NameTimeMethod
Parasite prevalence and density by molecular detection at the end of study cross-sectional survey.Month 18 (end of second transmission season; January-February 2020)

The primary outcome measure is parasite prevalence in the cross-sectional survey conducted at the end of the transmission season of year 2. If CCM and MSAT result in the early detection of infections, parasite prevalence at the end of the study will be lower in these arms compared to the control arm.

Secondary Outcome Measures
NameTimeMethod
Parasite prevalence and density by molecular detection at the end of year 1 cross-sectional survey.Month 6 (end of first transmission season; January-February 2019)

Parasite prevalence and density in the cross-sectional survey conducted at the end of the transmission season of year 1. If CCM and MSAT result in the early detection of infections, parasite prevalence will be lower in these arms compared to the control arm.

Parasite prevalence and density by molecular detection at the end of dry season cross-sectional survey.Month 12 (prior to second transmission season; June 2019)

Parasite prevalence and density in the cross-sectional survey conducted at the end of the dry season. If CCM and MSAT result in the early detection of infections, parasite prevalence will be lower in these arms compared to the control arm.

Gametocyte prevalence and or density in P. falciparum infections at the end of study cross-sectional surveyMonth 18 (end of second transmission season; January-February 2020)

Gametocyte prevalence in qPCR detected infections is assessed by molecular methods and compared between study arms.

Gametocyte prevalence and or density in P. falciparum infections at the end of year 1 cross-sectional surveyMonth 6 (end of first transmission season; January-February 2019)

Gametocyte density of male and female gametocytes will be assessed by molecular methods and compared between study arms.

Gametocyte prevalence and or density in P. falciparum infections at the end of dry season cross-sectional surveyMonth 12 (prior to second transmission season; June 2019)

Gametocyte density of male and female gametocytes will be assessed by molecular methods and compared between study arms.

Gametocyte prevalence and or density in P. falciparum during all study visitsThroughout study, an average of 18 months

Gametocyte density of male and female gametocytes will be assessed by molecular methods and compared between study arms.

The number of incident infections.Throughout study, an average of 18 months

Regular visits by CCM and MSAT will result in the identification of malaria infections that are not detected during passive case detection. The numbers of infections that are detected in each arm are quantified and compared between arms.

Infectivity to mosquitoes of P. falciparum infectionsThroughout study, an average of 18 months

For a selection of infections, infectiousness to mosquitoes is assessed by membrane feeding assays.

Trial Locations

Locations (1)

Centre National de Recherche et de Formation sur le Paludisme

🇧🇫

Ouagadougou, Burkina Faso

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