Prevalence and Independent Predictors of Malaria Infection Among Mobile and Nomadic Populations in North-eastern Nigeria: A Cross-sectional Study

Authors

  • Paul Moses Medugu
  • DanGa’anda Amos Tinsi

DOI:

https://doi.org/10.64321/jcr.v3i4.15

Keywords:

malaria; nomadic population; mobile population; prevalence; risk factors; LLIN; logistic regression.

Abstract

Mobile and nomadic populations may face increased malaria risk due to mobility, environmental exposure, limited preventive practices and restricted healthcare access. This study assessed malaria prevalence and independent predictors of infection among mobile and nomadic populations in North-Eastern Nigeria. A cross-sectional dataset of 500 participants from Adamawa, Bauchi, Borno, Gombe, Taraba and Yobe States was analyzed using descriptive statistics, Pearson's chi-square tests and multivariable logistic regression. Adjusted odds ratios (AORs) and 95% confidence intervals (CIs) were reported. Of the 500 participants, 157 (31.4%) were malaria-positive, with prevalence ranging from 24.6% in Yobe to 36.9% in Borno. Prevalence was significantly higher among participants near water (37.3%), non-LLIN users (38.0%), those with difficult healthcare access (37.0%) and those with poor malaria knowledge (38.5%). Multivariable analysis identified recent travel (AOR = 1.565, 95% CI: 1.012–2.421), proximity to water (AOR = 2.381, 95% CI: 1.522–3.723), non-use of LLINs (AOR = 2.341, 95% CI: 1.526–3.591), difficult healthcare access (AOR = 1.857, 95% CI: 1.212–2.845) and poor malaria knowledge (AOR = 2.348, 95% CI: 1.346–4.097) as independent predictors of malaria positivity. Malaria burden among mobile and nomadic populations is associated with environmental, mobility, preventive and healthcare-related factors. Integrated, mobility-sensitive malaria-control strategies are recommended.

Author Biographies

Paul Moses Medugu

Department of Mathematics and Statistics, Federal Polytechnic Mubi, Nigeria.

DanGa’anda Amos Tinsi

Department of Mathematics and Statistics, Federal Polytechnic Mubi, Nigeria.

References

Ahmed A, Mulatu K, Elfu B (2021). Prevalence of malaria and associated factors among under- five

children in Sherkole refugee camp, Benishangul-Gumuz region, Ethiopia. A cross- sectional

study. PLoS ONE.;16:e0246895.

Akpodiete NO, Diabate A, Tripet F (2019). Effect of water source and feed regime on development and phenotypic quality in Anopheles gambiae (s.l.): prospects for improved mass-rearing techniques towards release programmes. Parasit Vectors.;12:210.

Ducrotoy MJ, Revie CW, Shaw AP, Musa UB, Bertu WJ, Gusi AM (2017).. Wealth, household heterogeneity and livelihood diversification of Fulani pastoralists in the Kachia Grazing Reserve, northern Nigeria, during a period of social transition. PLoS One.;12(3):e0172866

The Editors of Encyclopaedia Britannica (2022). Fulani. Encyclopaedia Britannica; 2022

Folarin OF, Kuti BP, Oyelami AO (2021). Prevalence, density and predictors of malaria parasitaemia among ill young Nigerian infants. Pan Afr Med J.;40:25.

Mission Africa (2016). Belfast: Mission Africa. [Accessed 3 December 2016]. Available: http://www.missionafrica.org.uk/ministries/ 14/engaging-the-nomadic-fulani-in-nigeria

Mkali HR, Reaves EJ, Lalji SM, Al-mafazy A-W, Joseph JJ, Ali AS (2021). Risk factors associated

with malaria infection identified through reactive case detection in Zanzibar, 2012–2019.

Malar J.;20:485

Nyasa RB, Fotabe EL, Ndip RN (2021). Trends in malaria prevalence and risk factors associated with the disease in Nkongho-mbeng; a typical rural setting in the equatorial rainforest of the South West Region of Cameroon. PLoS ONE;16:e0251380.

Sani N. (2022). Malaria Transmission and Asymptomatic Malaria during Rainy Season among Nomads, North-eastern Nigeria Int. J. Trop. Dis. Health, vol. 43, no. 23, pp. 1-9, 2022

Shayo FK, Nakamura K, Al-Sobaihi S, Seino K (2021). Is the source of domestic water associated

with the risk of malaria infection? Spatial variability and a mixedeffects multilevel

analysis. Int J Infect Dis;104:224–31.

Talapko J, Škrlec I, Alebić T, Jukić M, Včev A (2019). Malaria: the past and the Present. Microorganisms.;7:179.

Tarekegn M, Tekie H, Dugassa S, Wolde-Hawariat Y (2021). Malaria prevalence and associated risk factors in Dembiya district, North-western Ethiopia. Malar J.;20:372

Tetteh JA, Djissem PE, Manyeh AK (2023). Prevalence, trends and associated factors of malaria in

the Shai-Osudoku District Hospital, Ghana. Malar J.;22:131-137

The Oxford English Dictionary (11th edition) https://www.oxfordlearnersdiction aries.com/definition/english/nomathdic, Accessed on 6 December, 202

WHO. World malaria report (2022). Global Malaria Programme. Geneva: WHO; 2022

Woday A, Mohammed A, Gebre A, Urmale K (2019). Prevalence and Associated Factors of Malaria among Febrile Children in Afar Region, Ethiopia: A Health Facility based study. Ethiop J Health Sci.;29:613–22. 16.

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Published

2026-08-31

How to Cite

Paul Moses Medugu, & DanGa’anda Amos Tinsi. (2026). Prevalence and Independent Predictors of Malaria Infection Among Mobile and Nomadic Populations in North-eastern Nigeria: A Cross-sectional Study. Journal of Current Research and Studies, 3(4), 155–162. https://doi.org/10.64321/jcr.v3i4.15