Evidence map›Paper›PMID 40392858›Full record

ArticlePLOS global public health2025

Comparing and integrating human mobility data sources for measles transmission modeling in Zambia.

Natalya Kostandova, Christine Prosperi, Simon Mutembo, Chola Nakazwe, Harriet Namukoko, Bertha Nachinga, Shengjie Lai, Andrew J Tatem, Qianwen Duan, Elliot N Kabalo and 19 more

Abstract read
In one paragraph

Article in PLOS global public health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. 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

29 authors.

Natalya KostandovaDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.ORCID https://orcid.org/0000-0002-6184-531X
Christine ProsperiDepartment of International Health, International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.
Simon MutemboDepartment of International Health, International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.
Chola NakazweInformation, Research and Dissemination, Zambia Statistics Agency, Lusaka, Zambia.
Harriet NamukokoPopulation and Social Statistics, Zambia Statistics Agency, Lusaka, Zambia.
Bertha NachingaInformation, Research and Dissemination, Zambia Statistics Agency, Lusaka, Zambia.
Shengjie LaiWorldPop, School of Geography and Environmental Science, University of Southampton, Southampton, United Kingdom.
Andrew J TatemWorldPop, School of Geography and Environmental Science, University of Southampton, Southampton, United Kingdom.
Qianwen DuanWorldPop, School of Geography and Environmental Science, University of Southampton, Southampton, United Kingdom.
Elliot N KabaloZambia Information and Communications Technology Authority, Lusaka, Zambia.
Kabondo MakungoZamtel, Lusaka, Zambia.ORCID https://orcid.org/0000-0003-3116-545X
Gershom ChongweTropical Diseases Research Centre, Ndola, Zambia.
Innocent ChilumbaBiomedical Sciences Department, Tropical Diseases Research Centre, Ndola, Zambia.
Gloria MusukwaAdministration, Macha Research Trust, Choma, Zambia.
Kalumbu H MatakalaClinical Research Department, Macha Research Trust, Choma, Zambia.
Mutinta HamahuwaClinical Research Department, Macha Research Trust, Choma, Zambia.
Webster MufwambiAdministration, Tropical Diseases Research Centre, Ndola, Zambia.
Japhet MatobaMolecular Biology Department, Macha Research Trust, Choma, Zambia.
Irene MutaleBiomedical Sciences Department, Tropical Diseases Research Centre, Ndola, Zambia.
Kenny SitutuBiomedical Sciences Department, Tropical Diseases Research Centre, Ndola, Zambia.
Edgar SimulunduAdministration, Macha Research Trust, Choma, Zambia.
Phillimon NdubaniAdministration, Macha Research Trust, Choma, Zambia.
Alvira Z HasanDepartment of International Health, International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.
Shaun A TrueloveDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.
Amy K WinterDepartment of Epidemiology and Biostatistics, University of Georgia, Athens, GeorgiaUnited States of America.
Andrea C CarcelenDepartment of International Health, International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.ORCID https://orcid.org/0000-0001-6271-6387
Bryan LauDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.
William J MossDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.ORCID https://orcid.org/0000-0001-6579-3513
Amy WesolowskiDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.ORCID https://orcid.org/0000-0001-6320-3575

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quantifying population mobility is crucial in developing accurate models of infectious disease dynamics. Increasingly, multiple data sources are available to describe individual and population mobility in a single location; however, there are no methods to systematically integrate these data. Combining information from these data sets may be valuable and help mitigate inherent biases in each data set due to sampling, censoring, and recall. We examined four commonly used data sources (mobile phone records, travel survey, Demographic and Health Survey, and Facebook location information) to quantify subnational travel patterns in Zambia. First, we explored summary metrics of mobility from each data set. Estimates of the probability of a trip and location of travel varied across data sets, with some data quantifying twice the frequency of travel as others. Then, we developed a departure-diffusion model that is able to produce a single estimate of travel by combining these data sets. When multi-data set models included mobile phone records, this data source dominated estimates given the broader spatial coverage. We then used a metapopulation model to simulate a measles outbreak to identify how these different data sets and models would impact estimates of the spatial spread of a highly infectious disease. We found that using travel survey data to parameterize mobility resulted in the introduction of cases in 98% of districts compared to less than 50% when mobile phone data or Facebook data were used. This study highlights the need for methods that facilitate integrating multiple data sets to improve validity of mobility estimates and resultant infectious disease transmission dynamics.

Identifiers

PMID40392858
PMCPMC12091742

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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.