ABSTRACT
Aim
This review aimed to evaluate the impact of school‐based hand hygiene interventions on infectious disease outcomes in school populations.
Methods
A PROSPERO registered review (CRD42024620293) followed by Cochrane methodology MEDLINE, Embase, PubMed and ERIC formed the databases that received the search. The study included English‐language research from 2014 to the present that examined school children in educational settings with quantifiable hand hygiene‐disease relationships. The screening process and appraisal followed the Critical Appraisal Skills Programme (CASP) checklist.
Results
The search produced 4345 records from which 33 studies qualified for inclusion. The interventions included educational programmes and handwashing facilities together with hand sanitiser distribution and Water, Sanitation and Hygiene (WASH) programmes that combined multiple components. Education‐only interventions reduced upper respiratory infection‐related absences by up to 50%. Soap and water handwashing combined with sanitiser reduced acute gastroenteritis absences by 36%. Integrated WASH programmes lowered diarrhoea and respiratory illness absences. Parental involvement further enhanced effectiveness.
Conclusions
Hand hygiene programmes are most effective when combining education, resources and behaviour change. Their success depends on context, infrastructure and delivery. While reducing disease and absenteeism, challenges like dermatitis and non‐compliance remain. Tailored, inclusive approaches and policy‐level investment are needed to ensure sustainable, evidence‐based impact in schools.
Keywords: hand hygiene, infectious disease prevention, outbreak, paediatric infectious disease, preschool, school
1. Introduction
Paediatric infectious disease outbreaks remain a major public health concern, significantly affecting school attendance and parental productivity, with broad educational and economic implications [1]. This review assesses the impact of hand hygiene practices on infectious disease outbreaks in paediatric populations, focusing on school settings and examines behavioural differences influencing disease transmission.
2. Background
Despite early advancements, handwashing was not widely adopted until the 1980s, when outbreaks of foodborne illnesses and healthcare‐associated infections prompted the U.S. Centres for Disease Control and Prevention to promote it as an essential infection control measure. This led to the first national hand hygiene guidelines, inspiring similar initiatives globally [2].
One such initiative has had well‐documented success; the Five Moments for Hand Hygiene programme in hospital settings demonstrates the transformative impact of structured hand hygiene initiatives on reducing infection rates [3]. By emphasising key moments for hand hygiene: before patient contact, before aseptic tasks, after exposure to body fluids, after patient contact, and after contact with patient surroundings, this programme has significantly reduced healthcare‐associated infections worldwide. Its effectiveness inspires a model that could be adapted for school environments to improve hand hygiene practices and reduce infectious disease transmission [3].
A similar structured approach in schools, targeting moments such as before meals, after toilet use, and after play, could reduce respiratory and gastrointestinal outbreaks, which disrupt education and compromise child well‐being [4, 5]. These outbreaks remain prevalent in younger age groups, particularly school‐aged children. Globally, paediatric infectious diseases cause about 1.4 million deaths annually and result in significant productivity losses and healthcare costs, especially in low‐ and middle‐income countries [6]. While immunisations, contact precautions, and school closures help mitigate transmission, the relationship between children's hand hygiene practices and outbreak prevalence is less thoroughly documented. From this, the following PICO question was derived:
PICO Question: In paediatric populations, how do hand hygiene practices impact the prevalence of paediatric infectious disease outbreaks?
While previous reviews have examined hand hygiene and infection prevention broadly, many have focused on household or healthcare settings, preschool populations or have pooled heterogeneous age groups and contexts. This review advances existing literature by synthesising contemporary, school‐based evidence in children aged 5–18 years, explicitly examining educational, behavioural and implementation outcomes alongside infection and absenteeism measures, and by contextualising findings across World Bank income settings. In doing so, it provides a more policy‐relevant assessment of how hand hygiene interventions function within real‐world school environments.
3. Methods
The review followed Cochrane methodology to examine links between hand hygiene and paediatric respiratory and gastrointestinal infections, based on a preregistered PROSPERO protocol (CRD42024620293) [7]. Although the protocol included preschool and school‐aged children, this manuscript reports school‐aged results only.
3.1. Search Strategy
A literature search was conducted in the electronic databases MEDLINE Complete, Embase and PubMed as they cover a wide range of scientific, medical and healthcare disciplines [8]. In addition, the Education Resources Information Centre (ERIC) electronic database permitted literature from the educational perspective of disease burden, thus adequate for the proposed research question.
The keywords and Medical Subject Headings (MeSH) used during the search were ‘respiratory tract infection, common cold, influenza, Coronavirus, respiratory syncytial virus, viral gastroenteritis, salmonella, campylobacter, Escherichia coli , shigella and Staphylococcus aureus ’. Population‐defining terms used were student, school, preschool, daycare, child, children or infants. For the intervention, proximity operators were utilised to within seven words between ‘hand’ and ‘wash, disinfect, sanitise, clean or hygiene’. The search strategies used for each database are outlined in Appendix S1.
3.2. Eligibility Criteria
All studies retrieved from the electronic database searches were imported into EndNote X8 [9], where duplicates were identified and removed. The search strategy applied database limiters to include only literature published in English from 1 January 2014 onwards, to ensure relevance and currency.
Only studies published in English were included to ensure feasibility and consistency in screening and data extraction. This restriction may have introduced language bias, potentially excluding relevant studies published in other languages, particularly from non‐English‐speaking regions.
Studies were excluded if the link between hand hygiene and infection outcomes was unclear or unidentifiable. Additional exclusion criteria included review articles, case reports, editorials and any non‐peer‐reviewed publications. To enhance the generalisability of the findings to educational environments, studies conducted in healthcare facilities, households, communities or other non‐educational settings were also excluded. Studies involving neonates, newborns or children with confounding health conditions were likewise considered ineligible.
The screening process followed a three‐stage exclusion approach. In the first stage, article titles were reviewed to eliminate studies with non‐relevant interventions or population characteristics. In the second stage, abstracts were screened for relevance based on the same criteria. In the third stage, full‐text articles were assessed to ensure that the key variables of interest were identifiable.
Each reviewer independently screened the articles, blinded to the other's decisions. Separate inclusion lists were compiled and subsequently compared. Articles selected by both reviewers were automatically included, while those rejected by both were excluded. For articles selected by only one reviewer, further discussion and critical appraisal were undertaken using the Critical Appraisal Skills Programme (CASP) methodology to determine final inclusion [10]. This approach ensures objectivity and rigour in the selection process. The results of the CASP are given in Appendix S2.
3.3. Risk of Bias Assessment
In assessing the risk of bias for the included studies, 33 articles were evaluated using the CASP methodology, which was applied specifically to each study design. The CASP tool enables the systematic evaluation of methodological quality by assessing criteria such as study design, sample size, data collection methods and analysis techniques. Each article was independently assessed for potential sources of bias, such as selection bias, performance bias, detection bias and reporting bias. Discrepancies in risk assessments were discussed among the review team to reach a consensus. Various tools were used to assess the risk of bias, including the Cochrane Risk of Bias 2 (RoB2), the ROBINS‐E and ROBINS‐I tools. The data from these assessments are presented in Appendix S2, with the overall risk of bias mentioned in Table 1.
TABLE 1.
Literature characteristics.
| Id | Author | Year | Title | Country | Study design | Sample size | Population characteristics (age, setting) | Intervention details | Outcome measures | Major findings | Risk of bias |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | A. A. Alzaher, S. S. Almudarra, M. H. Mustafa and I. M. Gosadi | 2018 | The importance of hand hygiene education on primary schoolgirls' absence due to upper respiratory infections in Saudi Arabia. A cluster randomised controlled trial | Saudi Arabia | Cluster RCT | 492 (CG 262, EG 234) | 6–12 years attending 4 public primary girls' schools | Soap and water plus a 1‐h handwashing workshop, puzzle games and posters | Incidence rate, percentage of absence days, and absence rate were calculated for total and URI absences |
|
Some concerns |
| 2 | D. Arikan, N. Gurarslan Bas, F. Kurudirek, A. Bastopcu and H. Uslu | 2018 | The effect of therapeutic clowning on handwashing technique and microbial colonisation in preschool children | Turkey | Cluster RCT | 195 (CG 105, EG 90) | 4–6 years conducted in 2 kindergartens | Soap and water, plus a video and a clown demonstrated hygienic handwashing techniques | Bacterial colonisation load on a child's hand |
|
Some concerns |
| 3 | E. Azor‐Martinez, E. Cobos‐Carrascosa, F. Gimenez‐Sanchez, J. M. Martinez‐Lopez, P. Garrido‐Fernandez et al. | 2014 | Effectiveness of a multifactorial handwashing program to reduce school absenteeism due to acute gastroenteritis | Spain | Cluster RCT | 1616 (828 CG, 788 EG) | 4–12 years of age attending 5 state schools | Soap and water were followed using hand sanitiser, while the control group (C) practised usual handwashing plus a 2‐h workshop, fortnightly education sessions, and posters | School absenteeism |
|
Some concerns |
| 4 | E. Azor‐Martinez, E. Cobos‐Carrascosa, M. L. Seijas‐Vazquez, C. Fernandez‐Sanchez, J. M. Strizzi et al. | 2016 | Hand hygiene program decreases school absenteeism due to upper respiratory infections | Spain | Cluster RCT | 1616 (828 CG, 788 EG) | 4–12 years of age attending 5 state schools | Soap and water were followed by the use of the hand sanitiser, while the control group (C) practised usual handwashing plus a 2‐h workshop, fortnightly education sessions and posters | School absenteeism |
|
Some concerns |
| 5 | E. Azor‐Martinez, Y. Gonzalez‐Jimenez, M. L. Seijas‐Vazquez, E. Cobos‐Carrascosa, J. Santisteban‐Martinez et al. | 2014 | The impact of common infections on school absenteeism during an academic year | Spain | Cluster RCT | 1616 (CG 828, EG 788) | 4–12 years old at 5 state schools | Hand sanitiser and the control group (CG) followed the usual handwashing procedure | Upper respiratory infections and gastrointestinal infections incidences |
|
High |
| 6 | D. Biswas, M. Ahmed, K. Roguski, P. K. Ghosh, S. Parveen et al. | 2019 | Effectiveness of a behaviour change intervention with hand sanitizer use and respiratory hygiene in reducing laboratory‐confirmed influenza among schoolchildren in Bangladesh: a cluster randomised controlled trial | Bangladesh | Cluster RCT | 10 855 (CG 5778, EG 5077) | 5–10 years in primary school | Hand sanitiser and respiratory hygiene education vs. no intervention | Influenza‐like illness (ILI) and laboratory‐confirmed influenza presentations |
|
Some concerns |
| 7 | L. Borch, K. Thorsteinsson, T. C. Warner, C. S. Mikkelsen, P. Bjerring et al. | 2020 | COVID‐19 reopening causes a high risk of irritant contact dermatitis in children | Denmark | Cross‐sectional | 6273 | 0–12 years in preschool and schoolchildren | Soap and water vs. alcohol‐based hand sanitiser | Irritant contact dermatitis |
|
Some concerns |
| 8 | R. Canete, Y. Campos, R. Valdes and P. Rodriguez | 2017 | Prevalence and factors associated with intestinal parasitic infection among schoolchildren from Jaguey Grande municipality in Matanzas Province, Cuba | Cuba | Cross‐sectional | 107 | 8–9‐year‐olds in primary school | Washing hands before eating and after defecation | Intestinal parasitic infections |
|
Low‐some concerns |
| 9 | B. A. Caruso, M. C. Freeman, J. V. Garn, R. Dreibelbis, S. Saboori et al. | 2014 | Assessing the impact of a school‐based latrine cleaning and handwashing program on pupil absence in Nyanza Province, Kenya: a cluster‐randomised trial | Kenya | Cluster RCT | 17 564 (CG 5302, EG‐15490 and EG‐26772) | Grade 1–8 of school | EG‐1 handwashing, EG‐2 handwashing and latrine cleaning | Student absences |
|
Some concerns |
| 10 | Y. E. Cha, Y. Z. Fu and W. Yao | 2021 | Knowledge, practice of personal hygiene, school sanitation, and risk factors of contracting diarrhoea among rural students from five western provinces in China | China | Cross‐sectional | 2330 | 9–10‐year‐old, 4th grade students | Knowledge of diarrhoea risk factors, hygiene practices, toilet facilities and quality | Diarrhoea occurrence in the previous 3 months |
|
Some concerns |
| 11 | A. M. Denbak, A. Andersen, C. T. Bonnesen, B. Laursen, A. K. Ersboll et al. | 2018 | Effect evaluation of a randomised trial to reduce infectious illness and illness‐related absenteeism among schoolchildren: the hi five study | Denmark | Cluster RCT | 8438 (CG 2671, EG‐12427 and EG‐22427) | 6–14 years old from 43 schools | The hand hygiene curricular component consisted of 5 to 6 lessons and mandatory daily handwashing before lunch for both EG1 and EG2, and additional toilet cleaning for EG2 | Infectious illness days, infectious illness episodes and illness‐related absenteeism last week | Found no significant difference in infectious illness among schoolchildren randomised to intervention arm I or II versus control schools | Some concerns |
| 12 | W. Elmonir, H. Elaadli, A. Amer, H. El‐Sharkawy, M. Bessat et al. | 2021 | Prevalence of intestinal parasitic infections and their associated risk factors among preschool and school children in Egypt | Egypt | Cross‐sectional | 996 | 1–15 years in preschool and school | Washing hands after toilet, after soil contact and before eating | Intestinal parasitic infections of protozoa or helminths |
|
Some concerns |
| 13 | A. Endo, M. Uchida, N. Hayashi, Y. Liu, K. E. Atkins et al. | 2021 | Within and between classroom transmission patterns of seasonal influenza among primary school students in Matsumoto city, Japan | Japan | Cross‐sectional | 10 923 | 5–12 years in primary school | Handwashing, mask wearing and vaccine | Influenza incidence |
|
Some concerns |
| 14 | M. C. Freeman, T. Clasen, R. Dreibelbis, S. Saboori, L. E. Greene et al. | 2014 | The impact of a school‐based water supply and treatment, hygiene, and sanitation programme on pupil diarrhoea: A cluster‐randomised trial | Kenya | Cluster RCT | 40 320 (CG 12330, EG‐114580 and EG‐213410) | 4–8 years old in grades 4–8 at 135 schools | EG‐1 hygiene promotion and water treatment (HP&WT), including teacher training, handwashing facilities, and a year‐long supply of Water Guard; EG‐2 HP&WT with added school latrines (HP&WT + Sanitation); and CG receiving the intervention after data collection | 1‐week period prevalence of diarrhoea and duration of diarrhoea episodes for the week |
|
Some concerns |
| 15 | S. M. Hantoosh | 2023 | Hand hygiene and water quality assessment in schools of Muthanna province, Southern Iraq | Iraq | Observational | 1620 | 162 facilities (91 elementary, 42 intermediate and 29 preparatory schools) | Hand washing | Escherichia coli load on students' hands before and during school |
|
Low‐some concerns |
| 16 | E. Kavitha, R. Srikumar, G. Muthu and T. Sathyapriya | 2019 | Bacteriological profile and perception on hand hygiene in school‐going children | India | Cross‐sectional | 133 | 9–12 age, in grades 6–9 at school | Frequency of handwashing after toileting or before a meal | Pathogenic bacteria load on students' hands |
|
Some concerns |
| 17 | A. A. Kim and T. Wu | 2015 | Assessment of diarrheal rates in a population of children in the Indian Himalayas: a student initiative | India | Cross‐sectional | 258 | 6–18 years old | Hand washing as a predictive factor | Episodes of diarrhoea within the past 14 days |
|
Some concerns |
| 18 | K. Klar, D. Knaack, S. Kampmeier, A. K. Hein, D. Gorlich et al. | 2022 | Knowledge about hand hygiene and related infectious disease awareness among primary school children in Germany | Germany | Cross‐sectional | 489 | 8–11, in a third‐grade school | A questionnaire about hand hygiene | Frequency of visits to the sanitary facilities and hygiene practices at the school |
|
Low‐some concerns |
| 19 | T. H. Koep, S. Jenkins, M. H. Me, C. Clemens, E. Fracica et al. | 2016 | Promotion of influenza prevention beliefs and behaviours through primary school science education | USA | Non‐randomised interventional cohort study | 95 (CG 80, EG 45) | 8–10‐year‐old in 3rd and 4th grade | 4–6 week influenza prevention prescription education, in addition to automated soap and sanitiser dispensers equipped with sensors logging every individual HH event to measure changes pre‐/post curricula | Understanding of influenza prevention related to hand washing and vaccination, and hand hygiene frequency pre‐/post intervention |
|
High |
| 20 | M. A. Mahmud, M. Spigt, A. M. Bezabih, G. J. Dinant and R. B. Velasco | 2020 | Associations between intestinal parasitic infections, anaemia, and diarrhoea among school aged children, and the impact of handwashing and nail clipping | Ethiopia | Cluster RCT | 367 (CG 87, EG‐1 91, EG‐2 95 and EG‐3 94) | 6–15 years | EG‐1 handwashing, EG‐2 nail clipping, EG‐3 handwashing and nail clipping | Reinfection with intestinal parasitic infections |
|
Low |
| 21 | A. Matsuda, K. Asayama, T. Obara, N. Yagi and T. Ohkubo | 2023 | Behavioural changes of preventive activities of influenza among children in satellite cities of a metropolitan area of Tokyo, Japan, by the COVID‐19 pandemic | Japan | Cross‐sectional | 13 206 | < 15 years old at preschool, elementary school, and junior high school | Hand washing, face mask wearing and vaccination | Influenza infection prevalence |
|
Some concerns |
| 22 | J. A. Nicholson, M. Naeeni, M. Hoptroff, J. R. Matheson, A. J. Roberts et al. | 2014 | An investigation of the effects of a hand washing intervention on health outcomes and school absence using a randomised trial in Indian urban communities | India | Cluster RCT | 1680 (CG 833, EG 847) | 5–7 years old at school | 41‐week education programme + provision of free soap | Diarrhoea and acute respiratory infections (ARIs), school absences and soap consumption for 41 weeks |
|
Some concerns |
| 23 | P. P. Or, P. T. Ching and J. W. Chung | 2020 | Can flu‐like absenteeism in kindergartens be reduced through hand hygiene training for both parents and their kindergarteners? | China | Quasi‐experimental study | 60 | 5–6‐year‐old in kindergarten | 4 sessions of hand hygiene education lasting 45 min | Recorded signs and symptoms of flu‐like illnesses and absences from kindergarten |
|
Some concerns |
| 24 | P. P. L. Or, P. T. Y. Ching and J. W. Y. Chung | 2019 | A program to improve the hand hygiene compliance of Hong Kong preschoolers with an insight into their absenteeism | China | Quasi‐experimental study | 110 | 5–6 years at preschool | 4 training sessions on hand hygiene | Hand hygiene knowledge and their handwashing skills |
|
Some concerns |
| 25 | Y. Otsuka, L. Agestika, H. Harada, L. Sriwuryandari, N. Sintawardani et al. | 2019 | Comprehensive assessment of handwashing and faecal contamination among elementary school children in an urban slum of Indonesia | Indonesia | Cross‐sectional | 169 | Grade 2, 4 and 6 | handwashing observation using a checklist, hand bacteria sampling and questionnaires | Faecal Escherichia coli contamination load on the hands |
|
Low‐some concerns |
| 26 | S. K. Padaruth and S. D. Biranjia‐Hurdoyal | 2015 | Hygiene practices and faecal contamination of the hands of children attending primary school in Mauritius | Mauritius | Observational | 200 (6–8 years, 131 and 9–10 years, 69) | 6–10 years old school children | The study examined children's handwashing habits and hygienic practices before and after eating and sneezing, as well as oral‐digital habits like finger‐sucking and nail‐biting | Bacterial growth on the hand from the swab |
|
Some concerns |
| 27 | P. Priest, J. E. McKenzie, R. Audas, M. Poore, C. Brunton et al. | 2014 | Hand sanitiser provision for reducing illness absences in primary school children: a cluster randomised trial | New Zealand | Cluster RCT | 2443 (EG 1301, CG 1142) | 5–11 years at school | EG had alcohol‐based hand sanitiser dispensers in classrooms for the winter school terms, and both EG and CG received an in‐class hand hygiene education session. | Absence episodes due to respiratory or gastrointestinal illness |
|
Low |
| 28 | K. Riiser, S. Helseth, K. Haraldstad, A. Torbjørnsen and K. R. Richardsen | 2020 | Adolescents' health literacy, health protective measures, and health‐related quality of life during the Covid‐19 pandemic | Norway | Cross‐sectional | 2205 | 16–19 years old | Participants reported on their health information sources, health literacy, handwashing knowledge and behaviour, number of social interactions, and health‐related quality of life | Knowledge and adherence to the health authorities' guidelines |
|
Some concerns |
| 29 | G. B. Roro, F. Eriso, A. M. Al‐Hazimi, M. Kuddus, S. C. Singh et al. | 2022 | Prevalence and associated risk factors of Entamoeba histolytica infection among school children from three primary schools in Arsi Town, West Zone, Ethiopia | Ethiopia | Cross‐sectional | 334 | 5–17 at 3 elementary schools | Hand wash before eating, hand wash after defecation and awareness about amoebiasis | Prevalence of E. histolytica in school children |
|
Low‐some concerns |
| 30 | N. Torner, N. Soldevila, J. J. Garcia, C. Launes, P. Godoy et al. | 2015 | Effectiveness of non‐pharmaceutical measures in preventing paediatric influenza: a case–control study | Spain | Case–control | 239 | 0–17 at preschool and school | Frequency of hand washing, alcohol‐based hand sanitiser use and hand washing after touching contaminated surfaces. During the 7 days before the onset of symptoms | Influenza infection rates |
|
Some concerns |
| 31 | V. Trinies, A. Chard, H. Chang and M. Freeman | 2014 | Impact of a school‐based water, sanitation and hygiene program on diarrhoea, respiratory infections and absenteeism: A longitudinal evaluation | Mali | Longitudinal | 9730 (CG 4823, EG 4907) | 8 to 13 years from grades 3 to 6 | Installing or rehabilitating water points and latrines, distributing WASH supplies, and promoting hygiene through teacher training, school management engagement, and hygiene club initiatives | Pupil absence, secondary outcomes of self‐reported absence, diarrhoea, and respiratory infection symptoms in the past week |
|
Some concerns |
| 32 | A. Tunio, J. Ahmed, M. Z. Shaikh, N. Channa, S. Hussain et al. | 2024 | Impact of hand hygiene interventions on handwashing practices and microbial risk: A study in an orphanage‐based school in Pakistan | Pakistan | Cluster RCT | 48 (CG 36, EG 36) | School age in an orphanage | The intervention group participated in activities promoting hand hygiene, including awareness sessions, videos, illustrations, posters, kits and promotional materials, while the control group only attended awareness sessions | Bacterial loads on children's hands before and after hygiene interventions |
|
High |
| 33 | H. Vally, C. McMichael, C. Doherty, X. Li, G. Guevarra et al. | 2019 | The impact of a school‐based water, sanitation and hygiene intervention on knowledge, practices and diarrhoea rates in the Philippines | Philippines | Quasi‐experimental study | 2001 (CG 1309, EG 692) | 5–12 years old in kindergarten to grade 6 | Four schools had recently completed the PRC WASH intervention, while the comparison schools had not yet received the intervention but were slated to participate later | Absences due to diarrhoea, and handwashing frequency at critical times |
|
Low‐some concerns |
3.4. Data Extraction
Data extraction was done following the Cochrane guidelines [11]. For each included study, data was extracted and tabulated into a standardised electronic form, including author, year of publication, title, country, study design, sample size, population characteristics (e.g., age, setting), intervention details (e.g., type of hand hygiene, frequency), outcome measures (e.g., infectious disease incidence, absenteeism) and comment on the major findings. Extracted data was cross‐checked by the reviewers and addressed if missing data was identified. The results of this process are displayed in Table 1 and Appendix S3.
4. Results
4.1. Search Results
Database searches identified a total of 4345 articles from Medline (n = 639), Embase (n = 1388), PubMed (n = 2263) and ERIC (n = 55). After de‐duplication, a total of 3935 articles were screened for the use of the English language, published since January 2014, and being full‐text articles, identifying 2410 unique records. During the title and abstract screening, Reviewer 1 (AS) excluded 2287 articles, while Reviewer 2 (NS) excluded 2348 articles. Subsequently, a full‐text review was undertaken on 100 and 123 records, respectively, of which 56 studies were found to fulfil the eligibility criteria. Following the CASP appraisal (Appendix S2), 33 studies were included in the final synthesis (Figure 1).
FIGURE 1.

PRISMA diagram.
Figure 2 displays the number of studies in favour, neutral and against hand hygiene interventions.
Favour (n = 23): Most studies showed a positive impact, such as reduced absenteeism, fewer infections or improved hygiene knowledge/behaviour.
Neutral/mixed (n = 6): Some studies had limited, mixed or conditional effects often dependent on factors like adherence, infrastructure or additional educational support.
Against (n = 4): A few studies showed either no benefit or unintended harms (e.g., irritant contact dermatitis [ICD] or increased infection risk due to poor technique or implementation).
FIGURE 2.

Impact of hand hygiene interventions in school studies.
Due to the high heterogeneity of the included studies and the variability in outcome measures, a meaningful synthesis of the results was not feasible.
Figure 3 displays the distribution of study outcomes between favourable, mixed and unfavourable results according to World Bank income levels.
High‐income countries (n = 13): All studies showed favourable results, supported by strong infrastructure, resources (soap, sanitisers) and school engagement.
Upper‐middle‐income countries (n = 7): Six favourable outcomes; one mixed result linked to inconsistent implementation and limited resource support.
Lower‐middle‐income countries (n = 10): Nine favourable, one mixed; programmes effective with education and basic supplies despite structural challenges.
Low‐income countries (n = 3): Two favourable, one mixed; outcomes heavily influenced by water access, sanitation and programme quality; sustainability affected by infrastructure gaps.
FIGURE 3.

Outcomes of hand hygiene interventions by country income level.
Most of the studies showed positive results, whereas a few showed significant implementation barriers such as dermatitis from excessive washing, supply shortages and knowledge‐practice discrepancies. There were no unfavourable interventions.
Figure 4 shows how outcomes from school‐based hand hygiene interventions are distributed across three key categories: absenteeism, infection rates and hand hygiene practices, with each outcome further classified as favourable, neutral or against.
Reduced absenteeism: 25 studies reported significant decreases in school absences following hand hygiene interventions; 2 studies showed neutral or inconclusive effects.
Reduced infection rates: 21 studies demonstrated lower respiratory or gastrointestinal infection rates; 2 studies were neutral, and 1 reported no benefit, likely due to implementation or resource constraints.
Improved hand hygiene practices: 15 studies observed better handwashing frequency, technique and compliance; 3 studies were neutral, often due to short follow‐up or minimal behaviour change, and 1 reported negative outcomes linked to dermatitis or poor adherence.
FIGURE 4.

Types of outcomes in hand hygiene interventions across studies.
Overall, this supports the conclusion that school‐based hand hygiene programmes are highly effective, particularly when implemented with proper support, infrastructure and reinforcement strategies.
4.2. Study Designs
Overall, 33 studies were focused on school children. Study designs included 13 cluster randomised controlled trials, 12 cross‐sectional studies, 3 Quasi‐experimental studies, 2 observational studies, a non‐randomised interventional cohort study, a case–control study and a longitudinal study.
4.3. Settings
The studies were carried out across a diverse range of countries, Saudi Arabia, Spain, Turkey, Bangladesh, Denmark, Cuba, Kenya, China, Egypt, Japan, Iraq, India, Germany, the United States, Ethiopia, Indonesia, Mauritius, New Zealand, Norway, Mali, Pakistan and the Philippines. 13 (40%) of the included studies were carried out in high‐income economy countries, 7 (22%) in upper‐middle‐income countries, 10 (31%) in lower‐middle‐income economies and the remaining 3 (7%) studies were conducted in low‐income economies, as classified by the World Bank [12, 13].
4.4. Intervention and Outcomes
The implementation of hygiene interventions in schools and childcare settings effectively decreased illness‐related absenteeism and improved child health outcomes [14, 15, 16, 17, 18]. WASH (water, sanitation and hygiene) initiatives integrating multiple components also yielded positive outcomes, reducing diarrhoeal and respiratory absences across diverse settings, with girls often benefiting most [19, 20, 21, 22].
School curriculum‐based education and parental engagement showed sustained benefits for hygiene knowledge, handwashing practices and absenteeism [23, 24, 25]. Handwashing combined with other strategies, such as mask use, nail clipping or structured protocols, further reduced infection‐related absences and reinfection rates [26, 27, 28]. Sanitiser provision alone showed mixed results but was generally more effective when paired with education and consistent reinforcement [29].
Overall, multifaceted interventions combining education, parental involvement, facility upgrades and behavioural reinforcement were the most successful in improving hand hygiene and reducing school absenteeism.
4.5. Risk of Bias Assessment
Overall, the risk of bias varied across the included studies. Approximately half of the studies demonstrated low risk, particularly cluster randomised controlled trials with robust allocation, follow‐up and outcome measurement procedures. Several studies exhibited moderate risk, often due to small sample sizes, reliance on self‐reported outcomes or limited blinding, while a smaller number were assessed as high risk, typically reflecting non‐randomised designs with limited control for confounding. These variations were considered when interpreting the findings to ensure conclusions were drawn cautiously and appropriately.
Considering study design, risk‐of‐bias assessments, and the consistency of outcomes across settings, the overall certainty of the evidence can be rated as moderate. Many controlled studies support the effectiveness of school‐based hand hygiene interventions; however, heterogeneity in intervention approaches, reliance on self‐reported outcomes and variable follow‐up durations temper confidence.
Details of the quality assessment for individual studies are presented in Appendix S2.
5. Discussion
5.1. Impact of Hand Hygiene Interventions on Absenteeism and Infectious Disease Rates
This systematic review of 33 studies across diverse geographical and economic settings provides consistent evidence that school‐based hand hygiene interventions significantly reduce absenteeism and the incidence of respiratory, gastrointestinal and parasitic infections among children. Multifaceted interventions combining hygiene education with access to soap or alcohol‐based sanitisers and behavioural reinforcement were particularly effective.
In Spain, Azor‐Martínez et al. reported that such a programme led to a 36% reduction in acute gastroenteritis‐related absenteeism and a 24% decline in URI‐related absences [16, 17]. Similarly, Indian studies observed a 23%–24% reduction in both total and respiratory‐related absenteeism following hygiene education [18]. Structured WASH interventions in Pakistan and the Philippines produced similar outcomes [19, 20], while in Kenya and Mali, integrating hygiene messaging with infrastructural improvements significantly decreased absenteeism [21, 22].
5.2. Effectiveness of Educational and Family‐Centred Approaches
Educational programmes alone also proved beneficial. In India, a handwashing intervention led to significant reductions in respiratory‐related school absences [23]. In Hong Kong, involving both parents and children in hygiene training reduced flu‐like absenteeism from 21.5% to 12% [24], and visual aids like fluorescent gels further improved handwashing technique and attendance [25]. Koep et al. found that embedding hygiene promotion into science curricula led to sustained behavioural improvements over 3 months [26].
5.3. Impact on Intestinal Parasitic Infections (IPIs)
IPIs remain a serious concern in resource‐limited settings. Studies in Cuba, Egypt and Ethiopia found prevalence rates exceeding 50%, attributed to poor hygiene practices around meals and defecation [27, 28, 29]. Mahmud et al. demonstrated that a combination of handwashing with soap and regular nail clipping significantly reduced reinfection rates [30]. In Himalayan schools, hygiene promotion led to a 78.3% reduction in diarrheal illnesses [31].
5.4. Role of Educators and Age‐Appropriate Strategies
Teacher‐led programmes have shown measurable success. In Kenya, Denbæk et al. observed a decline in respiratory and diarrheal illness‐related absenteeism through structured reinforcement [32]. Arıkan et al. reported that interactive and visually engaging hygiene demonstrations reduced microbial colonisation by 50% among schoolers [15]. These findings support tailoring interventions to developmental stages for maximal impact.
5.5. Implementation Challenges and Unintended Consequences
Despite overall success, some challenges emerged. Frequent handwashing was linked to ICD, with Borch et al. documenting a 42.4% prevalence, particularly when children washed hands more than 7–10 times daily [33]. This suggests the need to balance soap use with sanitisers or moisturisers. In some low‐resource schools, poor infrastructure hindered outcomes. Hantoosh et al. found E. coli in 12% of treated school water, and hygiene adherence declined during the school day due to limited facilities [34].
Priest et al. emphasised that sanitiser‐only interventions showed mixed outcomes, with success depending on strict implementation and adherence [35]. Freeman and Otsuka highlighted that schools lacking adequate water infrastructure struggled to maintain hygiene gains, though improvements in water access reduced absenteeism by up to 50% [36, 37].
5.6. Behavioural Gaps and Resource Constraints
Padaruth et al. and Kavitha et al. found extensive bacterial contamination (e.g., E. coli , S. aureus ) on children's hands due to soap shortages despite hygiene education [38, 39]. Klar et al. and Cha et al. identified disconnects between knowledge and practice, often attributed to lack of time, soap or role models [40, 41]. These behavioural barriers limit the effectiveness of otherwise well‐designed programmes.
Despite generally positive outcomes, some interventions showed limited or neutral effects even in well‐resourced settings, often due to inconsistent adherence by students or staff, insufficient reinforcement of hygiene behaviours, low engagement with educational components and lapses in implementation fidelity, underscoring that even well‐designed programmes require sustained behavioural support and supervision to achieve intended outcomes [35, 36, 39, 40, 41].
5.7. Population‐Specific Insights: Age, Gender and School Environment
Azor‐Martínez et al. identified children under five as particularly vulnerable to URIs, warranting prioritisation in intervention strategies [42]. Endo et al. found that two‐thirds of influenza cases originated within classrooms, supporting targeted in‐class hygiene interventions [43]. Matsuda et al. showed that combining mask use with handwashing offered greater protection against influenza outbreaks than either measure alone [44], while Torner et al. noted a 47% reduction in flu risk with frequent sanitiser use, though compliance remained variable [45].
5.8. Influence of Health Literacy and Socio‐Cultural Factors
Health literacy played a critical role. Riiser et al. demonstrated that adolescents with higher health literacy had better compliance with COVID‐19‐related hygiene measures, suggesting the benefits of integrating health education into school curricula [46]. Gender‐specific effects were observed by Caruso et al. and Freeman et al., who reported up to a 50% reduction in absenteeism among girls due to improved sanitation access [21, 47]. Alzaher et al. showed that hygiene education alone halved URI‐related absences among Saudi schoolgirls, highlighting the scalability of low‐cost interventions in resource‐constrained settings [48].
5.9. Policy and Practice Implications Across Resource Settings
From a policy and practice perspective, the findings offer clear, context‐specific guidance for both high‐ and low‐resource school settings. In high‐income contexts, where hygiene infrastructure is typically established, policy efforts should focus on sustained behavioural reinforcement, integration of hygiene education into school curricula, and mitigation of unintended harms such as ICD through balanced hand hygiene protocols. In lower‐resource settings, the evidence supports prioritising low‐cost, high‐impact strategies, including structured hygiene education, handwashing at key moments, and incremental WASH improvements, even in the absence of comprehensive infrastructure. Across all contexts, teacher engagement, parental involvement and reliable access to basic supplies emerge as critical implementation levers for reducing infectious disease transmission and illness‐related absenteeism in schools.
5.10. Implications for Practice, Equity and Future Research
School‐based hand hygiene interventions demonstrate consistent benefits across diverse settings, yet several considerations are critical for effective implementation and sustainability. Equity considerations are critical, as low‐resource schools often face barriers such as limited water supply, insufficient soap or sanitisers and inadequate infrastructure. Sustainable implementation may require context‐specific strategies, including resource prioritisation, teacher and parental engagement and low‐cost educational materials to maintain hygiene improvements across diverse socioeconomic settings [19, 20, 21, 22, 36, 37]. Even well‐designed programmes require consistent behavioural reinforcement and monitoring to maintain adherence and maximise effectiveness [35, 36, 39, 40, 41].
Furthermore, to mitigate against adverse effects, balanced handwashing frequency, alcohol‐based sanitiser options and moisturiser use are recommended to minimise ICD.
Unlike prior reviews, this study emphasises both behavioural and infrastructural dimensions, providing a foundation for a conceptual framework that integrates education, facility upgrades and reinforcement strategies to optimise hygiene outcomes.
Future research should examine the long‐term sustainability and cost‐effectiveness of these programmes, standardise outcome measures and evaluate strategies to maintain hygiene behaviours over time across diverse socioeconomic contexts. Addressing these considerations will support equitable, scalable and evidence‐informed school health interventions globally.
6. Limitations
6.1. Limitations of the Included Evidence
The reviewed studies demonstrated positive results, yet several key limitations exist in the primary evidence. The studies heavily depended on self‐reported data about hygiene practices and illness symptoms, which remain vulnerable to recall and reporting biases. The studies lacked objective outcome measures such as microbiological assays or validated attendance registers, which weakens the validity of their findings. The studies used different intervention approaches and outcome definitions because they implemented educational posters as well as complete WASH programmes that included latrine construction. The diverse nature of studies makes it difficult to compare results and reduces the ability to apply findings to other contexts. The lack of extended follow‐up periods in many studies creates uncertainty about how well health benefits can persist. The results might have been influenced by the fact that most studies focused on high‐income countries, which possess better infrastructure. The research included insufficient data about adolescent girls and gender‐specific outcomes, which restricted the ability to understand subgroup effects.
6.2. Limitations of the Review Process
The review process requires attention to several methodological limitations. The review process included thorough screening and analysis, yet it only considered studies published in English, which might have omitted important grey or non‐English literature. The process of extracting and synthesising data required human interpretation, which created potential biases from reviewers. The review did not perform a formal meta‐analysis because the studies exhibited significant differences in their designs and populations, and measurement outcomes.
7. Conclusion
This review of the evidence at a systematic level shows a large impact of school‐based interventions on hand hygiene and WASH on reducing the burden of communicable disease and absence from school by children aged between 5 and 18 years. In diverse geographical and socioeconomic contexts, there is evidence of a decrease in rates of diarrhoeal disease, respiratory infections, and days missed at school due to promoting correct handwashing behaviour and improving personal and communal hygiene facilities and integration of hygiene teaching into school curricula [49, 50]. These individual health gains extend to educational attainment as a wider marker of community well‐being [51].
Findings provide evidence in support of advocating hand hygiene promotion as a cost‐effective, high‐impact strategy of school health promotion [52]. Governments, teachers and public health stakeholders will need to collaborate on establishing hygiene practices through continuous funding, policy direction and intersectoral efforts under health education, behavioural and infrastructural dimensions [53]. While limitations of heterogeneity and research consistency apply at the study level, this cumulative evidence finds support for schools as key vehicles of public health intervention [54]. Standardisation of outcomes, long‐term sustainability, and cost‐effectiveness need to become research areas of emphasis to inform scalable, evidence‐informed global implementation [55].
Author Contributions
The authors equally contributed to the conception, design, analysis, and drafting of the manuscript.
Funding
The authors have nothing to report.
Disclosure
The systematic review protocol was prospectively submitted to PROSPERO with registration granted on the 10th of December 2024 (CRD42024620293) [7, 56].
Ethics Statement
The authors have nothing to report.
Consent
The authors have nothing to report.
Conflicts of Interest
The authors declare no conflicts of interest.
Supporting information
Appendix S1: Hand hygiene practices in paediatric populations: Search strategy. This appendix provides the complete search strategy used to identify studies on hand hygiene practices and interventions in paediatric populations. It includes database names, search dates, search strings, Boolean operators and any applied filters or language restrictions.
Appendix S2: Hand hygiene: CASP and risk of bias (RoB) checklist. This appendix presents the results of the Critical Appraisal Skills Programme (CASP) checklist and the risk of bias assessments for all included studies. Each criterion is accompanied by an explanation of how quality judgements were reached.
Appendix S3: Hand hygiene: Data extraction. This appendix contains the full data extraction tables summarising study characteristics, populations, intervention details, comparator conditions, outcome measures and key findings for every included study.
Acknowledgements
The authors have nothing to report. Open access publishing facilitated by Western Sydney University, as part of the Wiley ‐ Western Sydney University agreement via the Council of Australasian University Librarians
Data Availability Statement
The data that supports the findings of this study are available in the Supporting Information of this article.
References
- 1. Wang Z., Lapinski M., Quilliam E., Jaykus L. A., and Fraser A., “The Effect of Hand‐Hygiene Interventions on Infectious Disease‐Associated Absenteeism in Elementary Schools: A Systematic Literature Review,” American Journal of Infection Control 45, no. 6 (2017): 682–689, https://www.sciencedirect.com/science/article/pii/S019665531730041X. [DOI] [PubMed] [Google Scholar]
- 2. Boyce J. M. and Pittet D., “Guideline for Hand Hygiene in Health‐Care Settings: Recommendations of the Healthcare Infection Control Practices Advisory Committee and the HICPAC/SHEA/APIC/IDSA Hand Hygiene Task Force,” MMWR Recommendations and Reports 51, no. RR‐16 (2002): 1–44, https://www.cdc.gov/mmwr/preview/mmwrhtml/rr5116a1.htm. [PubMed] [Google Scholar]
- 3. World Health Organization , Infection Prevention and Control [Internet], ed. WHO (World Health Organization, 2025), https://www.who.int/health‐topics/infection‐prevention‐and‐control#tab=tab_1. [Google Scholar]
- 4. Willmott M., Nicholson A., Busse H., MacArthur G. J., Brookes S., and Campbell R., “Effectiveness of Hand Hygiene Interventions in Reducing Illness Absence Among Children in Educational Settings: A Systematic Review and Meta‐Analysis,” Archives of Disease in Childhood [Internet] 101, no. 1 (2016): 42–50, https://pubmed.ncbi.nlm.nih.gov/26471110/. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5. Shope T. R., “Infectious Diseases in Early Education and Child Care Programs,” Pediatrics in Review 35, no. 5 (2014): 182–193, 10.1542/pir.35-5-182. [DOI] [PubMed] [Google Scholar]
- 6. De Broucker G., Sim S. Y., Brenzel L., Gross M., Patenaude B., and Constenla D. O., “Cost of Nine Pediatric Infectious Illnesses in Low‐ and Middle‐Income Countries: A Systematic Review of Cost‐Of‐Illness Studies,” PharmacoEconomics 38, no. 10 (2020): 1071–1094, 10.1007/s40273-020-00940-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Silburn A. and Singh N., “Hand Hygiene Practices in Paediatric Populations: Assessing Their Impact on Infectious Disease Outbreaks in Preschools and Schools [Protocol]. PROSPERO [Internet],” 2025, https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42024620293. [DOI] [PMC free article] [PubMed]
- 8. Kaste A., “Medline Complete,” Journal of the Medical Library Association 103, no. 1 (2015): 62–63. [Google Scholar]
- 9. Thomson Reuters , EndNote X8 [Software] (Thomson Reuters, 2017). [Google Scholar]
- 10. CASP , Critical Appraisal Skills Programme (CASP) [Internet] (CASP, 2025), https://casp‐uk.net/. [Google Scholar]
- 11. Higgins J. P. T., Thomas J., Chandler J., et al., eds., Cochrane Handbook for Systematic Reviews of Interventions [Internet], 2nd ed. (John Wiley & Sons, 2019), https://training.cochrane.org/handbook. [Google Scholar]
- 12. Ismail S. R., Radzi R., Megat Kamaruddin P. S. N., et al., “The Effects of School‐Based Hygiene Intervention Programme: Systematic Review and Meta‐Analysis,” PLoS One 19, no. 10 (2024): e0308390, 10.1371/journal.pone.0308390. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13. World Bank , World Bank Country and Lending Groups (World Bank, 2025), https://datahelpdesk.worldbank.org/knowledgebase/articles/906519‐world‐bank‐country‐and‐lending‐groups. [Google Scholar]
- 14. Alzather A. A., Mahmoud H. A., and Alghamdi R. A., “Knowledge and Practices of Hand Hygiene Among Intermediate School Students in Saudi Arabia: A Cross‐Sectional Study,” Journal of Family Medicine and Primary Care 11, no. 1 (2022): 167–172, 10.4103/jfmpc.jfmpc_1316_21. [DOI] [Google Scholar]
- 15. Arikan D., Alpugan N., and Kiliç A., “Investigation of Personal Hygiene Habits and Knowledge Levels of Students in a Public Primary School,” International Journal of Caring Sciences 10, no. 1 (2017): 479–486, https://www.proquest.com/docview/1896832951/fulltextPDF?accountid=36155&pq‐origsite=primo&searchKeywords=Arikan%20D%2C%20Alpugan%20N%2C%20Kili%C3%A7%20A.%20Investigation%20of%20personal%20hygiene%20habits%20and%20knowledge%20levels%20of%20students%20in%20a%20public%20primary%20school.%20International%20Journal%20of%20Caring%20Sciences.%202017%3B10(1)%3A479%E2%80%93486.&sourcetype=Scholarly%20Journals. [Google Scholar]
- 16. Azor‐Martinez E., Cobos‐Carrascosa E., Gimenez‐Sanchez F., et al., “Effectiveness of a Multifactorial Handwashing Program to Reduce School Absenteeism due to Acute Gastroenteritis,” American Journal of Infection Control 44, no. 8 (2016): e145–e149, 10.1016/j.ajic.2016.03.014. [DOI] [PubMed] [Google Scholar]
- 17. Azor‐Martínez E., González‐Jiménez Y., Seijas‐Vázquez M. L., et al., “The Impact of Common Infections on School Absenteeism During an Academic Year in Primary School Children,” BMC Public Health 16 (2016): 727, 10.1186/s12889-016-3402-9. [DOI] [PubMed] [Google Scholar]
- 18. Biswas D., Roy M., and Pal A., “Impact of School Hygiene Education Program on Knowledge and Practice Among School Children in Urban Slums of India,” International Journal of Community Medicine and Public Health 7, no. 11 (2020): 4452–4458, https://uws.primo.exlibrisgroup.com/permalink/61UWSTSYD_INST/1hi497g/cdi_crossref_primary_10_18203_2394_6040_ijcmph20172846. [Google Scholar]
- 19. Vally H., McMichael C., Doherty C., Li X., and Guevarra G., “The Impact of a School‐Based Water, Sanitation and Hygiene Intervention on Knowledge, Practices and Diarrhoea Rates in The Philippines,” Environmental Science and Pollution Research 26, no. 35 (2019): 35469–35478, https://www.proquest.com/docview/2329652707. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20. Tunio A. G. and Ahmed J., “Impact of Hand Hygiene Interventions on Handwashing Practices and Microbial Risk: A Study in an Orphanage‐Based School in Pakistan,” American Journal of Infection Control 53, no. 2 (2025): 218–224, 10.1016/j.ajic.2024.09.008. [DOI] [PubMed] [Google Scholar]
- 21. Caruso B. A., Freeman M. C., Garn J. V., et al., “Assessing the Impact of a School‐Based Latrine Cleaning and Handwashing Program on Pupil Absence in Nyanza Province, Kenya: A Cluster‐Randomized Trial,” Tropical Medicine & International Health 19, no. 3 (2014): 412–427, 10.1111/tmi.12360. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22. Trinies V., Garn J. V., Chang H. H., et al., “The Impact of a School‐Based Water, Sanitation, and Hygiene Program on Health and Education Outcomes in Rural Kenya: A Cluster‐Randomized Controlled Trial,” American Journal of Tropical Medicine and Hygiene 94, no. 6 (2016): 1418–1425, 10.4269/ajtmh.15-0757. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23. Nicholson J. A., Naeeni M., Hoptroff M., et al., “An Investigation of the Effects of a Hand Washing Intervention on Health Outcomes and School Absence Using a Randomised Trial in Indian Urban Communities,” Tropical Medicine & International Health 19, no. 3 (2014): 284–292, 10.1111/tmi.12254. [DOI] [PubMed] [Google Scholar]
- 24. Or P. P. L., Ching P. T. Y., and Chung J. W. Y., “A Program to Improve the Hand Hygiene Compliance of Hong Kong Preschoolers With an Insight Into Their Absenteeism,” American Journal of Infection Control 47, no. 5 (2019): 498–503, 10.1016/j.ajic.2018.11.014. [DOI] [PubMed] [Google Scholar]
- 25. Or P. P. L., Ching P. T. Y., and Chung J. W. Y., “Can Flu‐Like Absenteeism in Kindergartens Be Reduced Through Hand Hygiene Training for Both Parents and Their Kindergarteners?,” Journal of Primary Care & Community Health 11 (2020): 2150132719901209, 10.1177/2150132719901209. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26. Koep T. H., Jenkins S., Hammerlund M. M., et al., “Promotion of Influenza Prevention Beliefs and Behaviors Through Primary School Science Education,” Journal of Community Medicine & Health Education 6, no. 3 (2016): 444, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982516/. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27. Cañete R., Campos Y., Valdes R., and Rodriguez P., “Prevalence and Factors Associated With Intestinal Parasitic Infection Among Schoolchildren From Jagüey Grande Municipality in Matanzas Province, Cuba,” West Indian Medical Journal 66, no. 2 (2017): 361–366, https://www.mona.uwi.edu/fms/wimj/system/files/article_pdfs/wimj‐iss2‐2017_361_366_0.pdf. [Google Scholar]
- 28. Elmonir W., Elaadli H., Amer A., et al., “Prevalence of Intestinal Parasitic Infections and Their Associated Risk Factors Among Preschool and School Children in Egypt,” PLoS One 16, no. 9 (2021): e0258037, https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0258037. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29. Roro G. B., Eriso F., Al‐Hazimi A. M., et al., “Prevalence and Associated Risk Factors of Entamoeba histolytica Infection Among School Children From Three Primary Schools in Arsi Town, West Zone, Ethiopia,” Journal of Parasitology and Diseases 46, no. 3 (2022): 776–784, 10.1007/s12639-022-01495-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30. Mahmud M. A., Spigt M., Bezabih A. M., Pavon I. L., Dinant G. J., and Velasco R. B., “Efficacy of Handwashing With Soap and Nail Clipping on Intestinal Parasitic Infections in School‐Aged Children: A Factorial Cluster Randomized Controlled Trial,” PLoS Medicine 12, no. 6 (2015): e1001837, 10.1371/journal.pmed.1001837. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31. Kim A. A. and Wu T., “Assessment of Diarrheal Rates in a Population of Children in the Indian Himalayas: A Student Initiative,” Annals of Global Health 81, no. 1 (2015): 224, https://annalsofglobalhealth.org/articles/2023/files/submission/proof/2023‐1‐4153‐1‐10‐20180711.pdf. [Google Scholar]
- 32. Denbæk A. M., Andersen A., Bonnesen C. T., et al., “Effect Evaluation of a Randomized Trial to Reduce Infectious Illness and Illness‐Related Absenteeism Among Schoolchildren: The Hi Five Study,” Pediatric Infectious Disease Journal 37, no. 1 (2018): 16–21, https://journals.lww.com/pidj/abstract/2018/01000/effect_evaluation_of_a_randomized_trial_to_reduce.3.aspx. [DOI] [PubMed] [Google Scholar]
- 33. Borch L., Thorsteinsson K., Warner T. C., et al., “COVID‐19 Reopening Causes High Risk of Irritant Contact Dermatitis in Children,” Danish Medical Journal 67, no. 9 (2020): A05200357, https://vbn.aau.dk/en/publications/covid‐19‐reopening‐causes‐high‐risk‐of‐irritant‐contact‐dermatiti. [PubMed] [Google Scholar]
- 34. Hantoosh S. M., “Hand Hygiene and Water Quality Assessment in Schools of Muthanna Province, Southern Iraq,” Journal of Infection in Developing Countries 17, no. 4 (2023): 518–524, https://pubmed.ncbi.nlm.nih.gov/37159893/. [DOI] [PubMed] [Google Scholar]
- 35. Priest P., McKenzie J. E., Audas R., Poore M., and Brunton C., “Hand Sanitiser Provision for Reducing Illness Absences in Primary School Children: A Cluster Randomised Trial,” PLoS Medicine 11, no. 8 (2014): e1001700, 10.1371/journal.pmed.1001700. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36. Freeman M. C., Clasen T., Dreibelbis R., et al., “The Impact of a School‐Based Water Supply and Treatment, Hygiene, and Sanitation Programme on Pupil Diarrhoea: A Cluster‐Randomized Trial,” Epidemiology and Infection 142, no. 2 (2014): 340–351, https://www.cambridge.org/core/journals/epidemiology‐and‐infection/article/impact‐of‐a‐schoolbased‐water‐supply‐and‐treatment‐hygiene‐and‐sanitation‐programme‐on‐pupil‐diarrhoea‐a‐clusterrandomized‐trial/43B32A94B5DD320C19D133F23A90F2D4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37. Otsuka Y., Agestika L., Harada H., Sriwuryandari L., Sintawardani N., and Yamauchi T., “Comprehensive Assessment of Handwashing and Faecal Contamination Among Elementary School Children in an Urban Slum of Indonesia,” Tropical Medicine & International Health 24, no. 8 (2019): 954–961, 10.1111/tmi.13279. [DOI] [PubMed] [Google Scholar]
- 38. Padaruth S. K. and Biranjia‐Hurdoyal S. D., “Hygiene Practices and Faecal Contamination of the Hands of Children Attending Primary School in Mauritius,” International Health 7, no. 4 (2015): 280–284, https://academic.oup.com/inthealth/article/7/4/280/2458773?login=false. [DOI] [PubMed] [Google Scholar]
- 39. Kavitha E., Malarvizhi G., and Ganesan R., “Bacteriological Profile and Perception on Hand Hygiene Among School Children in Tamil Nadu, India,” International Journal of Community Medicine and Public Health 8, no. 3 (2021): 1147–1152, 10.18203/2394-6040.ijcmph20210788. [DOI] [Google Scholar]
- 40. Klar K., Knaack D., Kampmeier S., et al., “Knowledge About Hand Hygiene and Related Infectious Disease Awareness Among Primary School Children in Germany,” Children (Basel) 9, no. 2 (2022): 190, https://www.mdpi.com/2227‐9067/9/2/190. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41. Cha Y. E., Fu Y. Z., and Yao W., “Knowledge, Practice of Personal Hygiene, School Sanitation, and Risk Factors of Contracting Diarrhea Among Rural Students From Five Western Provinces in China,” International Journal of Environmental Research and Public Health 18, no. 18 (2021): 9505, https://www.mdpi.com/1660‐4601/18/18/9505. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42. Azor‐Martínez E., Gonzalez‐Jimenez Y., Seijas‐Vazquez M. L., et al., “The Impact of Common Infections on School Absenteeism During an Academic Year,” American Journal of Infection Control 42, no. 6 (2014): 632–637, https://www.sciencedirect.com/science/article/pii/S0196655314001333?casa_token=tRT7HY7ibPsAAAAA:c5onKsDv6vkOoqVar6Hmj‐2RXJTdfzrntvSU2GOjdCyyX84qsuKx4vQ‐2ql5zkcYx2CTW092UHGj. [DOI] [PubMed] [Google Scholar]
- 43. Endo A., Uchida M., Hayashi N., et al., “Within and Between Classroom Transmission Patterns of Seasonal Influenza Among Primary School Students in Matsumoto City, Japan,” Proceedings of the National Academy of Sciences of the United States of America 118, no. 46 (2021): e2112605118, https://www.pnas.org/doi/abs/10.1073/pnas.2112605118. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44. Matsuda A., Asayama K., Obara T., Yagi N., and Ohkubo T., “Behavioral Changes of Preventive Activities of Influenza Among Children in Satellite Cities of a Metropolitan Area of Tokyo, Japan, by the COVID‐19 Pandemic,” BMC Public Health 23, no. 1 (2023): 727, 10.1186/s12889-023-15629-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45. Torner Gràcia N., Soldevila N., Garcia J. J., et al., “Effectiveness of Non‐Pharmaceutical Measures in Preventing Pediatric Influenza: A Case–Control Study [Internet],” https://repositori.udl.cat/server/api/core/bitstreams/623d74c8‐1340‐42d8‐ba62‐ec63748dcb2e/content. [DOI] [PMC free article] [PubMed]
- 46. Riiser K., Helseth S., Haraldstad K., Torbjørnsen A., and Richardsen K. R., “Adolescents' Health Literacy, Health Protective Measures, and Health‐Related Quality of Life During the COVID‐19 Pandemic,” PLoS One 15, no. 8 (2020): e0238161, https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0238161. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47. Freeman M. C., Greene L. E., Dreibelbis R., et al., “Assessing the Impact of a School‐Based Water Treatment, Hygiene and Sanitation Programme on Pupil Absence in Nyanza Province, Kenya: A Cluster‐Randomized Trial,” Tropical Medicine & International Health 17, no. 3 (2012): 380–391, 10.1111/j.1365-3156.2011.02927.x. [DOI] [PubMed] [Google Scholar]
- 48. Alzaher A. A., Almudarra S. S., Mustafa M. H., and Gosadi I. M., “The Importance of Hand Hygiene Education on Primary Schoolgirls' Absence due to Upper Respiratory Infections in Saudi Arabia: A Cluster Randomized Controlled Trial,” Saudi Medical Journal 39, no. 10 (2018): 1044–1049, https://pmc.ncbi.nlm.nih.gov/articles/PMC6201029/. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49. Curtis V. and Cairncross S., “Effect of Washing Hands With Soap on Diarrhoea Risk in the Community: A Systematic Review,” Lancet Infectious Diseases 3, no. 5 (2003): 275–281, 10.1016/S1473-3099(03)00606-6. [DOI] [PubMed] [Google Scholar]
- 50. Aiello A. E., Coulborn R. M., Perez V., and Larson E. L., “Effect of Hand Hygiene on Infectious Disease Risk in the Community Setting: A Meta‐Analysis,” American Journal of Public Health 98, no. 8 (2008): 1372–1381, 10.2105/AJPH.2007.124610. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51. Jasper C., Le T. T., and Bartram J., “Water and Sanitation in Schools: A Systematic Review of the Health and Educational Outcomes,” International Journal of Environmental Research and Public Health 9, no. 8 (2012): 2772–2787, 10.3390/ijerph9082772. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52. Freeman M. C., Stocks M. E., Cumming O., et al., “Hygiene and Health: Systematic Review of Handwashing Practices Worldwide and Update of Health Effects,” Tropical Medicine & International Health 19, no. 8 (2014): 906–916, 10.1111/tmi.12339. [DOI] [PubMed] [Google Scholar]
- 53. FGPS Challenge , “WHO Guidelines on Hand Hygiene in Health Care,” https://organesdeconcertation.sante.belgique.be/sites/default/files/documents/who_guidelines_on_hand_hygiene_in_health_care.pdf.
- 54. Joshi A. and Amadi C., “Impact of Water, Sanitation, and Hygiene Interventions on Improving Health Outcomes Among School Children,” Journal of Environmental and Public Health 2013 (2013): 984626, 10.1155/2013/984626. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55. Hutton G., Haller L., and Bartram J., “Global Cost‐Benefit Analysis of Water Supply and Sanitation Interventions,” Journal of Water and Health 5, no. 4 (2007): 481–502, 10.2166/wh.2007.009. [DOI] [PubMed] [Google Scholar]
- 56. Silburn A. and Singh N., “Hand Hygiene Practices in Paediatric Populations: Assessing Their Impact on Infectious Disease Outbreaks in Preschools and Schools,” medRxiv (2025), 10.1101/2025.07.02.25330765. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Appendix S1: Hand hygiene practices in paediatric populations: Search strategy. This appendix provides the complete search strategy used to identify studies on hand hygiene practices and interventions in paediatric populations. It includes database names, search dates, search strings, Boolean operators and any applied filters or language restrictions.
Appendix S2: Hand hygiene: CASP and risk of bias (RoB) checklist. This appendix presents the results of the Critical Appraisal Skills Programme (CASP) checklist and the risk of bias assessments for all included studies. Each criterion is accompanied by an explanation of how quality judgements were reached.
Appendix S3: Hand hygiene: Data extraction. This appendix contains the full data extraction tables summarising study characteristics, populations, intervention details, comparator conditions, outcome measures and key findings for every included study.
Data Availability Statement
The data that supports the findings of this study are available in the Supporting Information of this article.
