Evidence map›Paper›PMID 28592250›Full record

ArticleMalaria journal2017

Community-based intermittent mass testing and treatment for malaria in an area of high transmission intensity, western Kenya: study design and methodology for a cluster randomized controlled trial.

Aaron M Samuels, Nobert Awino, Wycliffe Odongo, Benard Abong'o, John Gimnig, Kephas Otieno, Ya Ping Shi, Vincent Were, Denise Roth Allen, Florence Were and 9 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Malaria journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07358767 (Determining the Impact of Malaria Mass Drug Administration on Malaria Prevalence in Under 15 Children and Pregnant Women), which is not on this map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT07358767 nacompletednot on this mapstarted 2021, after this paper: background citation

Determining the Impact of Malaria Mass Drug Administration on Malaria Prevalence in Under 15 Children and Pregnant Women

TypeinterventionalSponsorNoguchi Memorial Institute for Medical ResearchRan2021 to 2023Enrolled3,300ConditionsMalariaArmsArtemether-lumefantrine (AL)
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Mass testing and treatment on malaria in an area of western Kenya.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2021
    Article
  6. Article
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 4 institutions in 2 countries.

Aaron M SamuelsDivision of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, 30333, USA. iyp2@cdc.gov.
Nobert AwinoCentre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Wycliffe OdongoCentre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Benard Abong'oCentre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
John GimnigDivision of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, 30333, USA.
Kephas OtienoCentre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Ya Ping ShiDivision of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, 30333, USA.
Vincent WereCentre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Denise Roth AllenDivision of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, 30333, USA.
Florence WereCentre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Tony SangCentre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
David OborCentre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
John WilliamsonDivision of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, 30333, USA.
Mary J HamelDivision of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, 30333, USA.
S Patrick KachurDivision of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, 30333, USA.
Laurence SlutskerDivision of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, 30333, USA.
Kim A LindbladeDivision of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, 30333, USA.
Simon KariukiCentre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Meghna DesaiDivision of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, 30333, USA.
Kenya Medical Research Institute · KEDivision of Parasitic Diseases and Malaria · USCenters for Disease Control and Prevention · USCenter for Global Health · US

Funding

CGH CDC HHS U01 GH000048
6 · The paper itself

Abstract

Most human Plasmodium infections in western Kenya are asymptomatic and are believed to contribute importantly to malaria transmission. Elimination of asymptomatic infections requires active treatment approaches, such as mass testing and treatment (MTaT) or mass drug administration (MDA), as infected persons do not seek care for their infection. Evaluations of community-based approaches that are designed to reduce malaria transmission require careful attention to study design to ensure that important effects can be measured accurately. This manuscript describes the study design and methodology of a cluster-randomized controlled trial to evaluate a MTaT approach for malaria transmission reduction in an area of high malaria transmission. Ten health facilities in western Kenya were purposively selected for inclusion. The communities within 3 km of each health facility were divided into three clusters of approximately equal population size. Two clusters around each health facility were randomly assigned to the control arm, and one to the intervention arm. Three times per year for 2 years, after the long and short rains, and again before the long rains, teams of community health volunteers visited every household within the intervention arm, tested all consenting individuals with malaria rapid diagnostic tests, and treated all positive individuals with an effective anti-malarial. The effect of mass testing and treatment on malaria transmission was measured through population-based longitudinal cohorts, outpatient visits for clinical malaria, periodic population-based cross-sectional surveys, and entomological indices.

Indexed as

Research DesignAdolescentAdultAgedAged, 80 and overAntimalarialsChildChild, PreschoolCluster AnalysisCross-Sectional StudiesDiagnostic Tests, RoutineFemaleHumansInfantKenyaLongitudinal StudiesAntimalarialsAsymptomatic infectionsKenyaMalariaMass test and treatStudy designTransmission reduction

Identifiers

PMID28592250
PMCPMC5463392
OpenAlexW2623653996

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.