https://orcid.org/0000-0001-5883-9130
Figures
Abstract
Background
Soil-transmitted helminths pose a significant public health challenge among school-age children in developing countries, such as Ethiopia. This study determined the prevalence of soil-transmitted helminths, associated factors, and nutritional status of school-age children in Mekhoni town, Tigray, Ethiopia, 2025.
Methods
A school-based cross-sectional study design was conducted among 277 schoolchildren in Mekhoni town, Tigray, Ethiopia, from May 2024 to March 2025. A structured questionnaire was used to collect data on demographic characteristics of study participants, and stool samples were collected and processed using direct wet mount and Kato-Katz techniques. Anthropometric measurements were taken, and anthropometric indices were generated using the WHO AnthroPlus software to determine the nutritional status of schoolchildren. The data were analyzed using SPSS 27 software. Descriptive statistics were applied to present the data using frequency, tables, and figures. Bivariate logistic regressions were used to examine the correlation between the dependent variable and the individual independent variable, and multivariate logistic regressions were performed to determine the independent effect of the main explanatory variable on the outcomes of interest. A P-value < 0.05 was considered statistically significant.
Results
The overall prevalence of soil-transmitted helminth infections was 16.2% (n = 45), with Ascaris lumbricoides being the most identified parasite, at 10.1% (n = 28), followed by Trichuris trichiura at 6.1% (n = 17), and hookworms, at 2.9% (n = 8). Of the infected children, 31 (18.7%) were males, and 14 (12.6%) were females. The number of infections is also higher among children within the age group of 5–10, 22 (18.4%), than among those 11–14 years old, 23 (14.65%). Factors significantly associated with increased odds of infection were having large family size (AOR = 2.56, 95% CI: 1.18-5.55, P = 0.017), unclean fingernails (AOR = 2.63, 95% CI: 1.14-6.03, P = 0.022), untrimmed fingernails (AOR = 2.25, 95% CI: 1.006-5.03, P = 0.002), and lack of hand washing after visiting a toilet (AOR = 0.29, 95% CI: 0.13-0.63, P = 0.002). The overall prevalence of undernutrition was 37.5% (n = 104), with 22.2% being underweight (n = 117), 27.8% stunted (n = 77), and 11.19% wasted (n = 31). There was no statistically significant association between STH infection and nutritional status among study subjects.
Conclusion
The prevalence of STH infections was less than 20% (n = 45). The most common species of STH infections identified were Ascaris lumbricoides. The study also revealed a high prevalence of undernutrition among school-age children. Ensuring access to clean toilets and hand-washing facilities in the schools, introducing a school health and nutrition program are vital.
Author summary
Soil-transmitted helminth (STH) infections are a significant public health concern, especially in developing countries. This study examines the prevalence of STH infections and the nutritional status of school-age children in Mekhoni Town, Tigray, Ethiopia. The research found that the overall prevalence of STH infection in the study population was 16.2% (n = 45). Factors such as large family size, uncleaned fingernails, untrimmed fingernails, and handwashing practice after visiting a toilet were identified as significant contributors to the likelihood of STH infection. On the other hand, the study revealed that 37.5% (n = 104) of the children were undernourished, yet no statistical association was found between STH infection and undernutrition. These findings highlight the importance of improving hygiene practices and further exploring the relationship between STH infection and nutritional status in this region.
Citation: Deres A, Berhe B, Mulubirhan T, Bugssa G (2026) Soil-transmitted helminth infections and nutritional status of school-age children, in Mekhoni town, Tigray, Ethiopia. PLoS Negl Trop Dis 20(2): e0013932. https://doi.org/10.1371/journal.pntd.0013932
Editor: María Victoria Periago, Consejo Nacional de Investigaciones Cientificas y Tecnicas, Fundación Mundo Sano, ARGENTINA
Received: April 30, 2025; Accepted: January 13, 2026; Published: February 3, 2026
Copyright: © 2026 Deres et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All data underlying the findings of this study are fully available without restriction. The minimal dataset required to replicate all reported in the article is provided as a Supporting information file in SPSS (.sav) format (S1_Data.sav). The full thesis, which contains additional background materials, is publicly available in the Mekelle University institutional repository at: https://repository.mu.edu.et/items/e5841d4a-90bd-488b-80a8-abf43c32f7ba.
Funding: The author(s) received no specific funding for this work.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Ascaris lumbricoides, Trichuris trichiura, and hookworms are the three main parasitic worms that cause soil-transmitted helminthic infections (STHs) [1]. Although not routinely included in global or national deworming programs, Strongyloides stercoralis, which is transmitted through skin penetration by infective larvae, remains an important STH species and has been reported to be highly prevalent in Ethiopia [2]. A. lumbricoides and T. trichiura are transmitted through the fecal-oral route, where individuals become infected by ingesting eggs from contaminated water, surfaces, hands, or food. Hookworm infections are spread through the skin by contact with soil contaminated with infective larvae [3], ingestion of larvae [4], or through the transmammary route [5]. Low income, inadequate personal hygiene, poor environmental sanitation, restricted availability of clean water, and tropical climate are the factors linked with infection of STH [6]. South Asia, Southeast Asia, and Sub-Saharan Africa are the regions with the highest burden [4]. These parasitic infections continue to pose significant public health challenges, particularly among school-age children (SAC) in developing nations with limited resources [7,8]. Approximately 2 billion individuals worldwide carry at least one type of STH infection (with A. lumbricoides, 1 billion, T. trichiura, 800 million, and hookworm, 740 million). Besides, around 4 billion people are susceptible to contracting STH infections globally [9,10], causing an approximate 4.98 million years of disability adjusted life years (DALYs). Consequently, around 300 million individuals experience severe morbidity due to STH, leading to annual deaths ranging from 10,000 to 135,000 [11]. In Africa, it is estimated that around 90 million SAC are believed to have STH infections [12]. In Ethiopia, impacting over 79 million people, with approximately 25 million being SAC [13]. The nationwide occurrence rates of hookworms, A. lumbricoides, and T. trichiura stood at 16%, 37%, and 30%, respectively [8].
Despite the introduction of deworming initiatives and improvements in water, sanitation, and hygiene (WASH) practices in the region, the prevalence of STH infections among school-age children in Tigray remains approximately 10% [14]. The continued existence of these infections indicates that the root causes, such as poor sanitation, lack of access to clean water, and limited health education, have not been sufficiently addressed. Furthermore, in regions like Tigray, where there are internally displaced people due to war, managing infectious diseases becomes exceedingly complex and challenging [15]. On the other hand, the prevalence of stunting, underweight, and wasting among primary school-age children in Ethiopia was 21.3%, 18.2%, and 17.7% respectively [16]. Malnutrition and STH frequently occur together in the same area, affecting the same individuals simultaneously and perpetuating each other [17].
According to WHO recommendations, preventive chemotherapy (PC) through Mass Drug Administration (MDA) is the main strategy for controlling STH in school-aged children. WHO recommends annual deworming in areas where STH prevalence is between 20% and 50%, and biannual deworming where prevalence exceeds 50%. In settings with a prevalence below 20, routine MDA is not required, and selective treatment is advised [18].
In Ethiopia, school-based deworming for STH has been implemented since 2015 as part of the national NTD control program, and significant progress has been achieved in expanding MDA coverage among school-aged children. However, despite these national efforts, some segments of the population remain unreached [19]. In the present study area, specific data on MDA implementation is not available, highlighting the need for local epidemiological evidence.
The recent destructive war in the Tigray region of Ethiopia has probably worsened the challenges associated with STH infections and malnutrition among SAC in the study area. The interruption of essential services, displacement of communities, and breakdown of health care and sanitation infrastructure in the Tigray region could have heightened the prevalence and seriousness of these public health concerns. Undertaking this research in the post-conflict context to determine the prevalence of soil-transmitted helminths, associated factors, and nutritional status among school-age children in Mekhoni town, Tigray, Northern Ethiopia will produce vital evidence to steer the implementation of the recovery and rehabilitation endeavors, guaranteeing that the health and nutritional requirements of the vulnerable school-age population are adequately met.
Methods
Ethical statement
Ethical clearance was obtained from Mekelle University, College of Health Sciences Ethical Review Committee. Furthermore, a permission letter was obtained from the Tigray Regional Health Bureau and the Mekhoni Wereda Health office. Besides, further permission was obtained from the selected school’s administrator. Moreover, written informed consent was obtained from the families and/ or guardians of all participating children, and verbal assent was obtained from the children. Each piece of data was kept confidential. All children who were found positive for STH had their results communicated to their families and were linked to the nearest health facility for treatment according to national deworming guidelines.
Study setting
Mekhoni is a town situated 657 kilometers north of Addis Ababa, the capital city of Ethiopia, and 126 kilometers south of Mekelle, the capital city of the Tigray National Regional State. It is positioned at coordinates 12047’30’‘N and 12048’30’‘N latitude, and 39038’00’‘ and 39039’00’‘E longitude (Fig 1). Mekhoni sits at the center of Raya Azebo Woreda, which is bordered to the south by Alamata Woreda, to the north by Hintalo-Wajirat Woreda, to the west by Enda mekoni and Emba-Alaje, and to the east by the Afar Regional State of Ethiopia.
The district has a bimodal rainfall pattern, with light rains from February to April and heavier rains between July and September. On average, annual rainfall is about 724 mm. In the western highlands, daily temperature typically ranges from 13.93 °C to 18.3 °C, while in the valley, it is warmer, ranging from 19.64 °C to 23.44 °C. Around 90% of the district is considered “midland”, lying between 1,500 and 2,300 m above sea level, while the remaining 10% falls into the “lowland” category, below 1,500 m [20].
According to the projected population data from the Central Statistical Agency (CSA), Raya Azebo Wereda has a total population of 176,401, comprising 86,810 males and 88,591 females. Of these, 39,101 live in urban areas, while the majority, 137,300, reside in rural areas [21].
The economy of the population is heavily dependent on agricultural activities, which serve as the primary source of livelihood for most of its population. The region’s fertile lands support the cultivation of crops such as Sorghum, teff, and maize, while livestock farming also plays an important role in the local economy [22]. The town has a primary hospital, which provides inpatient and outpatient medical services to residents of Mekhoni town and Raya Azebo wereda. The town has four elementary schools, all of which have suffered significant damage to their sanitation and water facilities because of the recent devastating war.
Study design, objective, and study period
A school-based cross-sectional study was conducted to determine the prevalence of soil-transmitted helminths, associated factors, and nutritional status among school-age children in Mekhoni town, Tigray, Northern Ethiopia, from May 2024 to March 2025.
Eligibility criteria
School-age children who were willing to participate, provided stool samples, and obtained consent from their parents or legal guardians were included in the study.
Sample size and sampling technique
A sample size was determined using the single population proportion statistical formula, as shown below.
where n = required sample size, Z is the statistic that corresponds to the desired confidence level (95%), P is the estimated population proportion, and d is the margin of error (the desired precision of the estimate). Taking a prevalence of 21% as the best available estimate for the prevalence of STH infections from a previous study [23], a margin of error of 5%, a z-score of 1.96, and adding 10% for non-response resulted in a final sample size of 285.
Two elementary schools were chosen from the four available in Mekhoni town using simple random sampling. Once the schools were selected, students were stratified by their educational levels (grades 1–8). The allocation of schoolchildren to schools and grade levels was done proportionally based on the number of students in each school and grade [24]. Sections within the schools were selected using a lottery method. A roster containing the list of students was compiled as the sampling frame. To select study participants for each grade level, systematic random sampling was employed, following proportional allocation. The sampling interval (K) was calculated by dividing the total number of units in the population (N) by the desired sample size (n), resulting in a sampling interval of 11 (K = 11) across the two schools.
The first student was randomly selected from the Kth interval, and subsequent participants were chosen at every Kth interval thereafter (Fig 2).
Data collection procedure
Questionnaire.
Data on demographic characteristics, hygiene, and sanitation of study participants were collected using a structured and pre-tested questionnaire. Household information was obtained from parents or guardians, while child hygiene practice was asked directly to the child. All interviews were conducted at the school. The questionnaire was developed in English based on previous research works and translated into the local language (Tigrigna). The face-to-face interview was conducted by trained data collectors.
Anthropometric measurement.
Using standardized anthropometric measurements, weight and height were taken for all study participants. For weight measurement, children were asked to remove their shoes, wear light clothes, and remove accessories. Then, trained data collectors measured children’s weight on a calibrated portable digital scale (FAZZINI S759) and recorded the value to the nearest 0.1 kilograms. For height measurement, children were instructed to stand upright with their shoulders aligned, arms at their sides, thighs and heels touching comfortably together, the buttocks, scapulae, and head were positioned against the vertical backboard with a sliding head bar. The height was then recorded to the nearest 0.1 centimeter [25].
Parasitological investigation.
Labeled stool containers with tight covers bearing serial numbers of the subjects were supplied for the study participants. Fecal specimens were processed by wet mount and Kato-Katz techniques. Fresh stool samples (approximately 2 mg of stool) were put on a slide with the wooden applicator and emulsified with a drop of physiological saline (0.85%). The preparation was then covered with a cover slide and examined at 10× and 40 × microscopic objectives [26]. Thick smear was prepared using the Kato-Katz template, which delivers 41.7 mg of stool, and the smear was transported to Mekhoni Primary Hospital for further analysis. The slides were examined by an experienced laboratory technologist under 10-x and 40-x objective lenses for the presence of eggs of STH. Hookworm ova detection was performed by examination of the Kato-Katz slide within one hour of stool collection and its preparation. Furthermore, all eggs of STHs were counted under a microscope and reported as the number of eggs per gram of stool(EPG) by multiplying by the appropriate factor of 24 [27]. The intensity of the infection was estimated based on the cut-off value for the classification of infection intensity [28]. As light, moderate, and heavy infections. 1–4999 epg, 5000–49999 epg, and >50000 epg, respectively for A. lumbericoides for T. trichuira, 1–999 epg, 1000–9999 epg, and >10000 epg, and for hookworm, 1–1999 epg, 2000–3999 epg, and >4000 epg according to WHO cut-off values [29].
Data quality assurance and management
The Questionnaire was pre-tested in Baro Elementary School before actual data collection. The data collected were checked for consistency and accuracy daily. All the laboratory procedures were conducted as per the Standard Operating Procedures. Two slides were prepared from each sample and were independently examined by two Medical Laboratory Technologists. Additionally, 10% of the samples were randomly chosen and re-checked by senior medical Laboratory Technologists.
Data analysis and interpretation
All data was recorded by hard copy. After checking for completeness, data were coded and entered, using SPSS (Statistical Package for Social Sciences statistical software) version 27. Then Descriptive statistics were applied to present the data using frequency, tables, and figures. Binary logistic regression was employed to show the correlation of the dependent variable with the individual independent variable. Potential confounders were identified based on previous literature [23]. Variables with a p-value <0.25 in the bivariable analysis were included in the multivariable logistic regression model. Multivariate analysis was done to identify the independent effect of the main explanatory variable on the outcomes of interest after adjusting for several other confounding variables. A P-value of <0.05 was considered indicative of a statistically significant difference. The results of the logistic regression indicated that the chosen model was a good fit, as evidenced by the Hosmer-Lemeshow goodness-of-fit test, which yielded a P-value of 0.08. WHO AnthroPlus 2009 (v 1.0.4) was used to calculate weight-for-age z-scores (WAZ), height-for-age z-scores (HAZ), and BMI-for-age z-scores (BAZ). Children < -2SD were classified as Under-weight (WAZ < -2SD), Stunted (HAZ < -2SD), and Wasted (BAZ < -2SD) [30].
Operational definitions
- School-age children: children who attend primary school (one to eighth grade) and are in the age group of 5–14 years.
- Anthropometric measurements: are systematic measurements of the variation of physical dimensions and composition of the human body.
- Nutritional status: is the child’s state of the body, which is determined by anthropometric measurement indices as normal, stunted, wasted, or underweight based on the WHO standard reference 2007
- Undernutrition: is a poor nutritional status of primary schoolchildren, which is expressed in anthropometric indices when the Z-scores for the WHO standards of 2007 are less than minus two (Z-scores < -2SD)
- Underweight: weight-for-age z-scores below -2SD
- Severe underweight: weight-for-age z-scores below -3SD
- Stunting: height-for-age z-scores below -2SD
- Severe stunted: height-for-age z-score below -3SD
- Wasting: BMI-for-age z-scores below -2SD
- Severe wasted: BMI-for-age z-scores below -3SD
Results
Socio-demographic, hygienic, and environmental characteristics of the study participants
A total of 277 study participants were enrolled, with a response rate of 97.2%. Representing both Degol and Hayelom Araya Elementary Schools. Most were in the older age group, and the sex distribution was slightly male-dominant. In addition, information was collected on the key hygiene behaviors and household environmental conditions, including handwashing practices, access to safe water, waste disposal methods, and toilet availability. These characteristics are summarized in the combined table below (Table 1).
Prevalence of soil-transmitted helminths
A total of 45 (16.2%) study participants were found to be positive for one or more STH infections. Moreover, A. lumbricoides represented the most dominant STH parasite, affecting 10.1% (n = 28) of the study participants. T. trichiura and hookworm were detected in 6.1% (n = 17) and 2.9% (n = 8) of the schoolchildren, respectively. Of the infected children, 31 (18.7%) were males, and 14 (12.6%) were females (Table 2).
STH co-infections and intensity
The prevalence of single STH infection was 82.2% (37/45). A single infection by A. lumbricoides was the most predominant parasite, constituting 54% (20/37) of the infections. Co-infection by A. lumbricoides and T. trichiura was 75% (6/8) whereas A. lumbricoides and hookworm co-infections were 25% (2/8). The proportions of light infections for A. lumbricoides and Hookworm were 100%; only 2 cases of T. trichuira were with moderate infection intensity (Table 3).
Nutritional status and STH infection
The overall prevalence of under-nutrition was 37.5% (N = 104). Besides, 26 (22.2%) children aged 5–10 years were underweight, 77 (27.8%) of the children were stunted, and 31 (11.19%) of the children were wasted. The prevalence of severe forms of underweight among children aged 5–10 years (WAZ < -3SD), severe stunting (HAZ < -3SD), and wasting (BAZ < -3SD) was 5 (4.3%), 19 (6.9%) and 9 (3.2%) respectively.
Of the children with undernutrition, 26 (25%) of them were with STH infections. Among the children infected with STH, 27.3% were underweight (n = 117), 44.4% were stunted, and 20% were wasted. In comparison, the prevalence of underweight, stunting, and wasting among healthy children was 20% (n = 117), 24.5%, and 9.5%, respectively (Table 4).
Factors associated with STH infection
The family size of study participants, hand washing method after toilet, cleanness of fingernails, and trimming of fingernails were identified as independent factors associated with STH infection at a significant level of 0.05. Family size emerged as a strong predictor of STH, with participants from households of more than five members being more likely to be infected by STH than participants having a family size ≤5 (AOR = 2.56, 95% CI: 1.18-5.55, P = 0.017). Participants who washed their hands with both water and soap after using the toilet were 71% less likely to be infected with STH compared to those who washed with water only (AOR = 0.29, 95% CI: 0.13-0.63, P = 0.002). Additionally, children who did not clean their fingernails were 2.63 times more likely to be infected than those who did (AOR = 2.63, 95% CI: 1.14-6.03, P = 0.022). Likewise, children with untrimmed fingernails had a higher likelihood of STH infection compared to those with trimmed nails (AOR = 2.25, 95% CI: 1.006-5.03, P = 0.002). In bivariate logistic regression, undernutrition, stunting, and wasting were found to be statistically significant when STH infection status was considered as the outcome variable. However, these factors were no longer significant after adjusting for confounders in multivariate logistic regression (Table 5).
Discussion
A prevalence of 16.2% in our study area shows that transmission has been reduced compared with historically high levels in Ethiopia [13,31], but it has not been eliminated. By WHO programmatic thresholds, this sits below the 20% cut-off commonly used to trigger district-wide annual MDA [18], yet it remains high enough to warrant caution. Evidence from national mapping and recent reviews shows that Ethiopia’s progress has been uneven; many woredas have improved after repeated school-based preventive chemotherapy, while others continue to harbor persistent pockets of STH, often linked to uneven coverage and poor WASH conditions [31,32].
Within this context of uneven national progress, the prevalence in our study area is higher than reported rates from Wera-baye (6.6%) [33], Enderta wereda (6.5%) [34], Gurage zone (9.5%) [35], and Cameroon (2.2%) [36]. However, the prevalence in this study is lower than that observed in Fogera district (30.30%) [37], Yirgachefe (54.5%) [38], Dara Mallo and Uba Debretsehay districts (33.2%) [39], Mettu (84.4%) [40], and Jimma (55%) [30]. On the other hand, it is similar to findings from studies conducted in Adola (16.1%) [24], Ambo (12.8%) [41], and Western Kenya (17.0%) [42]. Variation in socio-demographic and economic factors, as well as differences in awareness regarding STH exposure, transmission, and prevention, may explain the discrepancies in prevalence between this study area and the others.
In terms of species, A. lumbericoides was the most common STH infection, with a prevalence rate of 10.1%. This is higher than the findings in Medebay Zana (1.71%) [43] and Gurage zone (3%) [35]. But lower than a study from Yirgachefe (21.7%) [38] and Mettu (39%) [40]. Though the prevalence of A. lumbericoides in the current study is consistent with previous studies in Dembecha (11.4%) [23], and Hawassa (11.2%) [44]. T. trichuira and Hookworm had prevalence rates of 6.1% and 2.9% respectively, which is higher than the one observed in Wera-abaye (1.6%, 0%) [33], and Enderta wereda (0.21%, 0.42%) [34]. Moreover, the prevalence rate in this study aligns with research conducted in Hawassa (4.5%, 2.7%) [44]. In contrast, hookworm infection is much lower than the study conducted in Durebte town (46.9%) [9]. The variation in the prevalence of specific parasites may be linked to variations in the suitability of the macro and microenvironments for the parasites across different regions, study time frame, geographical locations, urbanization, and lack of public health education, deworming practices, as well as economic, social, and cultural factors. As it has been described in literature [45].
This study found that factors such as family size, hand washing practices after using the toilet, fingernail cleanness, and trimmed fingernails were significantly linked to STH infections. Similarly, studies in Dembecha [23], Hawassa [44], and Ambo [41] also identified family size as a key risk factor for STH infection. In this study, children who washed their hands with both water and soap after using the toilet were 71% less likely to be infected with STH infections (AOR = 0.29, 95 CI (0.13-0.63), P = 0.002). Similar to a study conducted in Lurambi, Kenya [46]. Another report also highlighted the importance of nail trimming and cleanliness in relation to STH infection, which aligns with our findings [8].
Among the schoolchildren investigated, 37.5% were found to be suffering from undernutrition, which is higher than the rates in Addis Ababa (30.9%) [47] and Yirgachefe (28.9%) [38]. But lower than the rate reported from Debremarkos (56.2%) [48]. The stunting prevalence was found to be 27.8%, which is consistent with findings from studies in Agulae (25.5%) [49] and Jimma (21%) [30]. However, it was higher than the prevalence reported in Chencha (8.9%) [17]. In contrast, the prevalence was lower than studies conducted in Hawzen (33.3%) [50], Arbaminch (41.9%) [25], and Mulo district (42.4%) [51]. The prevalence of wasting was 11.9%. Which is lower compared to the study conducted in Agulae (44%) [49]. In spite of that, our result is higher than the rates reported in Yirgachefe (5.2%) [38] and Jimma (6.9%) [30]. The prevalence of underweight in the population being studied was found to be 22.2%, which is lower than the results reported in Agulae (55%) [49] and Hawzen (32.2%) [50]. On the other hand, it is higher than the prevalence observed in Addis Ababa (15.4%) [47], Yirgachefe (12.9%) [38], and Mettu (5.1%) [40]. The disparity in stunting, wasting, and underweight prevalence across different regions is possibly due to differences in factors such as socio-economic status, living conditions, improper child feeding practices, geographic differences, variations in agricultural productivity, urbanization, and healthcare for the children.
The lack of association between nutritional status and STH infection in this study is consistent with findings from Yirgachefe [38] and Chencha [17], unlike the study conducted in Jimma [30] and Mettu [40], in which T. trichiura is a predictor of stunting and undernutrition, respectively.
Limitations
This study shares the limitations of a cross-sectional study design, which does not establish a cause-and-effect relationship between dependent and independent variables. Additionally, the Kato-Katz technique has limited sensitivity, particularly for light-intensity infections, which may have led to underestimation of the true prevalence of STH infections. Strongyloides sterocolralis was not assessed, as it requires different diagnostic methods and a different treatment regimen than the STH species targeted by WHO’s preventive chemotherapy programs. Furthermore, the study relied solely on anthropometric measurements to assess nutritional status, without biochemical and dietary assessment.
Conclusion
The current study found that the prevalence of STH infections is less than 20%, indicating a low-risk category based on WHO classifications. The most common species of STH infections identified were Ascaris lumbricoides. Additionally, STH infections were linked to factors such as large family size, nail cleanness, nail trimming, and hand-washing practices after using the toilet. The study also revealed a high prevalence of undernutrition among school-age children; however, there was no significant difference in the nutritional status of children with or without STH infections. Ensuring access to clean toilets and hand-washing facilities in the school, promoting hygiene awareness and teaching good practice, and introducing a school health and nutrition program are vital to enhance the health and nutritional status of the schoolchildren.
Supporting information
S1 File. Questionnaire to assess socio-demographic, hygienic, and environmental factors associated with STH infection.
https://doi.org/10.1371/journal.pntd.0013932.s001
(DOCX)
S1 Table. All socio-demographic, hygiene, and environmental factors, along with statistical values.
https://doi.org/10.1371/journal.pntd.0013932.s002
(DOCX)
Acknowledgments
We would like to extend our sincere thanks to Mekelle University College of Health Sciences Division of Biomedical Sciences, Department of Medical Parasitology and Entomology for providing us the opportunity to undertake this research thesis. We are pleased to acknowledge Mekhoni Primary Hospital for giving us access to its laboratory facilities for analysis.
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