Evidence map›Paper›PMID 26482774›Full record

Trial reportBMJ open2015

Interrupting transmission of soil-transmitted helminths: a study protocol for cluster randomised trials evaluating alternative treatment strategies and delivery systems in Kenya.

Simon J Brooker, Charles S Mwandawiro, Katherine E Halliday, Sammy M Njenga, Carlos Mcharo, Paul M Gichuki, Beatrice Wasunna, Jimmy H Kihara, Doris Njomo, Dorcas Alusala and 13 more

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in BMJ open, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02397772 (The Impact of Different Treatment Strategies on the Transmission Dynamics of Soil-transmitted Helminths), which is not on this map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
–field-weighted citation impact
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.

NCT02397772 phase4completednot on this map

The Impact of Different Treatment Strategies on the Transmission Dynamics of Soil-transmitted Helminths: a Cluster Randomised Trial in Kenya

TypeinterventionalSponsorLondon School of Hygiene and Tropical MedicineRan2015 to 2017Enrolled21,761ConditionsHelminthiasis, Nematode Infection, Disease Transmission, InfectiousArmsalbendazole
3 · Its place in the literature

Who cites it

45 citing papers in PubMed.

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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

23 authors.

Simon J BrookerFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Charles S MwandawiroEastern and Southern Africa Centre of International Parasite Control, Kenya Medical Research Institute, Nairobi, Kenya.
Katherine E HallidayFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Sammy M NjengaEastern and Southern Africa Centre of International Parasite Control, Kenya Medical Research Institute, Nairobi, Kenya.
Carlos McharoEvidence Action, Nairobi, Kenya.
Paul M GichukiEastern and Southern Africa Centre of International Parasite Control, Kenya Medical Research Institute, Nairobi, Kenya.
Beatrice WasunnaEastern and Southern Africa Centre of International Parasite Control, Kenya Medical Research Institute, Nairobi, Kenya.
Jimmy H KiharaEastern and Southern Africa Centre of International Parasite Control, Kenya Medical Research Institute, Nairobi, Kenya.
Doris NjomoEastern and Southern Africa Centre of International Parasite Control, Kenya Medical Research Institute, Nairobi, Kenya.
Dorcas AlusalaNeglected Tropical Diseases Unit, Division of Communicable Disease Prevention and Control, Ministry of Health, Nairobi, Kenya.
Athuman ChiguzoOffice of the Executive Committee, Medical Services and Public Health, Kwale County Government, Kwale, Kenya.
Hugo C TurnerFaculty of Medicine, Department of Infectious Disease Epidemiology, London Centre for Neglected Tropical Disease Research, School of Public Health, St Mary's Campus, Imperial College London, London, UK.
Caroline TetiEvidence Action, Nairobi, Kenya.
Claire Gwayi-ChoreEvidence Action, Nairobi, Kenya.
Birgit NikolayFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
James E TruscottFaculty of Medicine, Department of Infectious Disease Epidemiology, London Centre for Neglected Tropical Disease Research, School of Public Health, St Mary's Campus, Imperial College London, London, UK.
T Déirdre HollingsworthWarwick Mathematics Institute, University of Warwick, Coventry, UK School of Life Sciences, University of Warwick, Coventry, UK.
Dina BalabanovaFaculty of Public Health and Policy, London School of Hygiene & Tropical Medicine, London, UK.
Ulla K GriffithsFaculty of Public Health and Policy, London School of Hygiene & Tropical Medicine, London, UK.
Matthew C FreemanDepartment of Environmental Health, Rollins School of Public Health, Emory University, Atlanta, Georgia, USA.
Elizabeth AllenFaculty of Epidemiology and Population Health, London School of Hygiene & Tropical Medicine, London, UK.
Rachel L PullanFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Roy M AndersonFaculty of Medicine, Department of Infectious Disease Epidemiology, London Centre for Neglected Tropical Disease Research, School of Public Health, St Mary's Campus, Imperial College London, London, UK.

Funding

Medical Research Council MR/N00597X/1Wellcome TrustWellcome Trust 098045Wellcome Trust MR/M021289/1
6 · The paper itself

Abstract

introductionIn recent years, an unprecedented emphasis has been given to the control of neglected tropical diseases, including soil-transmitted helminths (STHs). The mainstay of STH control is school-based deworming (SBD), but mathematical modelling has shown that in all but very low transmission settings, SBD is unlikely to interrupt transmission, and that new treatment strategies are required. This study seeks to answer the question: is it possible to interrupt the transmission of STH, and, if so, what is the most cost-effective treatment strategy and delivery system to achieve this goal? METHODS AND ANALYSIS: Two cluster randomised trials are being implemented in contrasting settings in Kenya. The interventions are annual mass anthelmintic treatment delivered to preschool- and school-aged children, as part of a national SBD programme, or to entire communities, delivered by community health workers. Allocation to study group is by cluster, using predefined units used in public health provision-termed community units (CUs). CUs are randomised to one of three groups: receiving either (1) annual SBD; (2) annual community-based deworming (CBD); or (3) biannual CBD. The primary outcome measure is the prevalence of hookworm infection, assessed by four cross-sectional surveys. Secondary outcomes are prevalence of Ascaris lumbricoides and Trichuris trichiura, intensity of species infections and treatment coverage. Costs and cost-effectiveness will be evaluated. Among a random subsample of participants, worm burden and proportion of unfertilised eggs will be assessed longitudinally. A nested process evaluation, using semistructured interviews, focus group discussions and a stakeholder analysis, will investigate the community acceptability, feasibility and scale-up of each delivery system. ETHICS AND DISSEMINATION: Study protocols have been reviewed and approved by the ethics committees of the Kenya Medical Research Institute and National Ethics Review Committee, and London School of Hygiene and Tropical Medicine. The study has a dedicated web site. TRIAL REGISTRATION NUMBER: NCT02397772.

Indexed as

AdolescentAdultAgedAged, 80 and overAlbendazoleAnthelminticsChildChild, PreschoolCommunicable Disease ControlCost-Benefit AnalysisCross-Sectional StudiesFemaleHookworm InfectionsHumansKenyaLongitudinal StudiesAlbendazoleAnthelminticsSoilEPIDEMIOLOGYPARASITOLOGYPUBLIC HEALTH

Identifiers

PMID26482774
PMCPMC4611208

What OpenQuestion holds

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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.