Hygiene practices, particularly hand and oral hygiene, are crucial for preventing both infectious and chronic diseases.1, 2 Since the COVID-19 pandemic, the significance of hand hygiene has gained renewed attention. 3 Hand hygiene is a simple yet highly effective method for minimizing the transmission of infectious diseases, including respiratory and gastrointestinal infections, which are prevalent in communal environments such as schools. Public health authorities emphasize handwashing as a key preventive strategy. 4, 5 Their guidelines recommend regular handwashing, especially before eating, after using the restroom, and after touching potentially contaminated surfaces. Similarly, oral hygiene plays a vital role in maintaining overall health and preventing various diseases. 6 Poor oral hygiene is linked to dental caries, periodontal diseases, and systemic conditions such as cardiovascular diseases and diabetes. 7 Moreover, inadequate oral hygiene can affect quality of life by causing dental pain, tooth loss, and oral infections, which impair eating, speaking, and social interactions, leading to psychological distress and reduced self-esteem. 8
While hand and oral hygiene are often studied independently, integrating these practices into a single study provides a more comprehensive understanding of personal hygiene behaviors. Both practices share common determinants, such as access to health education, socioeconomic factors, and personal habits, and they reflect broader health awareness and preventive behaviors. 9 Examining these hygiene practices together can help identify shared barriers and facilitators, which is critical for designing holistic health promotion strategies.
Adolescents, who are transitioning from childhood to adulthood, are particularly susceptible to developing poor hygiene habits that may persist into adulthood. Promoting good hygiene practices in this age group is important for improving long-term health outcomes. In China, where rapid urbanization and lifestyle changes impact health behaviors, understanding the state of hand and oral hygiene among adolescent students is essential. Despite the recognized importance of hygiene practices, there is limited research focusing specifically on hand and oral hygiene among Chinese adolescent students. Existing studies conducted in other countries may not be directly applicable to Chinese adolescent students due to unique cultural, environmental, and socioeconomic factors.10–13 The lack of region-specific data hinders our understanding of hygiene practices in China, emphasizing the need for targeted research.
This study seeks to fill the existing knowledge gap by investigating the prevalence of and factors influencing hand and oral hygiene behaviors among adolescent students in Zhejiang Province, Eastern China. Identifying the key factors influencing these practices will not only enhance hygiene behaviors in this population but also support the development of targeted public health policies that can reduce the incidence of infectious diseases and promote better overall health outcomes.
Materials and Methods Study Design and PopulationOur study utilized data derived from the 2022 Zhejiang Province Youth Risk Behavior Survey (YRBS) of China, an ongoing school-based, cross-sectional survey carried out by the Zhejiang Provincial Center for Disease Control and Prevention (CDC). Launched in 2007, the YRBS was designed to assess the prevalence of health-related behaviors and influencing factors among adolescent students, and it has been conducted every five years since its inception. The study population comprised all middle and high school students in 30 surveillance districts of Zhejiang Province. The participants were students with household registration in Zhejiang Province, excluding those from adult education institutions (eg, adult middle schools, adult high schools, and adult specialized secondary schools) and schools for students with disabilities.
A multistage stratified cluster sampling method, consisting of three stages, was employed to ensure economical and efficient sampling. In the first stage, data from all schools in 30 surveillance counties or districts were collected based on the sample framework of Zhejiang Province’s health surveillance districts. Schools were then categorized into three strata: middle schools, vocational high schools and academic high schools. In the second stage, within each stratum, classes were organized in sequence according to the geographic location of the surveillance site (from north to south and from west to east) and by grade level (from lower to higher grades). 706 classes out of 376 schools were selected by a simple random sampling technique. Finally, all adolescent students within the selected classes were surveyed. Detailed descriptions of the study design and sampling strategy are available in prior publication.14 During the sampling procedure, the Probability Proportional to Size (PPS) method was applied, ensuring that the proportion of students selected from each type of school (middle school, academic high school, and vocational high school) accurately reflected their relative distribution in the overall adolescent population.
Sample Size CalculationThe sample size was calculated using the following formula: where the parameters were defined as follows: the design effect (deff) was set at 5.0, P = 0.556 (the prevalence of poor oral hygiene practices among Chinese adolescents in 2003),15μ = 1.96, and the relative error,
with r = 0.1. Using these parameters, the sample size for each stratum was calculated to be 1535 cases. Considering the stratification of the study population into 12 strata (2 strata for urban and rural areas, 2 for gender, and 3 for school types) and adjusting for a non-response rate of 15.0%, the final required sample size for the survey was calculated to be 21,670 participants.
The questionnaire was specifically designed for this study, drawing on references from the Global School-based Student Health Survey (GSHS) and the US Youth Risk Behavior Surveillance System (YRBSS). It covered a broad range of topics, including sociodemographic details, awareness of hypertension, physical activity, overall health and quality of life, smoking habits, alcohol consumption, usage of mobile phone, dietary patterns, weight management, hygiene practices, among others. The data were collected using a self-administered questionnaire, which students completed collectively in their classrooms. Prior to the survey, investigators provided an explanation of the study’s purpose and importance, emphasizing the anonymity of the responses. Students were assured that their teachers and parents would not have access to their answers and that their participation would have no impact on their academic performance. To ensure privacy during the survey, students were seated at least one meter apart, and the classroom environment was kept quiet. Neither school doctors nor teachers were present during the survey process. Upon completion, students individually placed their questionnaires into a sealed collection box to maintain confidentiality.
This study was conducted in accordance with the ethical principles outlined in the Declaration of Helsinki. Ethical approval was obtained from the Zhejiang Provincial CDC’s ethics committee (Approval No: 2022–007-01). Written informed consent was obtained from all participating students. For students under 18 years of age, written informed consent was provided by a parent or legal guardian prior to their participation in the study.
Definition of the VariablesIn this study, oral and hand hygiene practices were primary outcome variables. Oral hygiene practice was assessed with the question, “In the past month, how many times did you usually brush your teeth per day”? The response options ranged from 1 (never brushed) to 6 (four or more times per day). For analysis, responses 1–3 were recoded as 1, indicating poor oral hygiene, and responses 4–6 were recoded as 0, indicating good oral hygiene practice. Hand hygiene practices were evaluated using three specific questions: (1) “In the past month, did you wash hands before meals”?; (2) “In the past month, did you wash hands after using the restroom”?; and (3) “In the past month, did you use hand sanitizer, soap, or liquid soap while washing hands”? Each of these questions had response options ranging from 1 (never) to 5 (always). For analysis, each question was dichotomized: “always” was recoded as 0, representing good hygiene, while all other responses were recoded as 1, representing poor hygiene. The study also collected sociodemographic data, including age, gender, parents’ marriage status, parental education levels, only-child status, school type, current living situation, household registration, and family economic status.
Statistical MethodsData collected by the self-administered questionnaire were input using EpiData software, and double-entry verification was conducted to ensure the accuracy of the data input. SAS software (version 9.4), was used to analyze the research data. Continuous variables were presented as mean ± standard deviation. Categorical data were summarized by reporting their frequencies and percentages. To examine the factors influencing poor oral and hand hygiene behaviors, a multivariate logistic regression analysis was employed. The significance level for statistical tests was set at α = 0.05.
Results General Characteristics of the ParticipantsIn this survey, 27,070 individuals were approached, yielding a high response rate of 96.53%. Out of these, 26,101 met the World Health Organization’s definition of adolescents (ages 10–19)16 and provided complete survey data. Table 1 summarizes the general characteristics of the participants. The average age of students was 15.92 ± 1.74 years, with most participants being 16 years or older (58.28%), followed by those aged 14–15 years (31.87%). The gender distribution was relatively balanced, with 13,456 boys (51.55%) and 12,645 girls (48.45%). A significant proportion of the participants were from rural areas (68.08%), compared to 31.92% from urban areas. The participants were predominantly from middle schools (47.05%), while 27.49% attended academic high schools and 25.45% vocational high schools. Most participants came from families with married parents (87.17%). The educational levels of the parents varied, with a majority of fathers (55.17%) and mothers (59.04%) having a middle school education or below. Additionally, 62.09% of the participants were not only children, and a slight majority (54.66%) lived outside school dormitories. Regarding family income, 85.80% of participants reported being from middle-income families.
Table 1 General Characteristics of the Subjects (n=26,101)
Prevalence of Poor Oral Hygiene PracticeTable 2 presents the prevalence of poor oral hygiene practices among the 26,101 adolescents, categorized by sociodemographic variables. Overall, 29.25% of participants exhibited poor oral hygiene, with boys (34.45%) showing a higher prevalence than girls (23.72%). Adolescents from rural areas reported a higher prevalence of poor oral hygiene (30.04%) compared to those from urban areas (27.59%). Vocational high school students showed the highest prevalence (30.48%), followed by middle school students (29.96%) and academic high school students (26.91%). Adolescents from non-traditional families (eg, divorced or separated) had a higher prevalence of poor oral hygiene (32.36%) compared to those from married families (28.79%). Poor oral hygiene was also more common among adolescents whose parents had lower educational attainment, with the highest prevalence observed in those whose fathers (32.25%) and mothers (31.83%) had a middle school education or below, and the lowest prevalence among those with college-educated parents (paternal: 22.52%, maternal: 22.24%). Adolescents who were not the only child had a slightly higher prevalence of poor oral hygiene (29.94%) compared to only children (28.13%). Adolescents from low/very low-income families exhibited the highest prevalence of poor oral hygiene (37.32%), compared to those from middle-income (29.33%) and high/very high-income families (23.01%).
Table 2 Prevalence of Poor Oral Hygiene Practice Among the Subjects (n=26,101)
Figure 1 illustrates the frequency of tooth brushing among boys, girls, and the overall participants. The majority (51.43%) reported brushing their teeth twice daily, with notable gender differences: 59.98% of girls versus 43.39% of boys reported brushing twice a day.
Figure 1 The frequency of tooth brushing among boys, girls, and the overall participants.
Prevalence of Poor Hand Hygiene PracticesTable 3 details the prevalence of poor hand hygiene practices among the adolescents. Overall, 78.06% reported poor hygiene before meals, 24.67% after using the toilet, and 82.56% when using soap. The prevalence of poor hand hygiene before meals and when using soap was higher among older adolescents (≥16 years), girls, rural residents, academic high school students, those from non-traditional families, adolescents whose parents had lower educational attainment, those living outside school dormitories, and those from lower-income families. In contrast, poor hand hygiene practice after using the toilet was more prevalent among younger adolescents (≤13 years), boys, urban residents, middle school students, those from non-traditional families, those with mothers who had higher educational attainment, only children, those living in school dormitories, and those from lower-income families.
Table 3 Prevalence of Poor Hand Hygiene Practices Among the Subjects (n=26,101)
Associated Factors of Poor Oral Hygiene PracticeMultivariable logistic regression analysis (Table 4) revealed that adolescents whose parents had other marital statuses (divorced, widowed, separated) were at higher risk of poor oral hygiene practices (OR: 1.18, 95% CI: 1.09–1.28). Conversely, being a girl (0.58, 0.55–0.62), attending an academic high school (0.83, 0.73–0.95), having a father with a high school education (0.87, 0.81–0.93) or higher (0.77, 0.69–0.85), having a mother with a high school education (0.91,0.85–0.98) or higher (0.76, 0.68–0.84), being an only child (0.91, 0.86–0.97), and having a middle (0.77, 0.69–0.86) or high/very high family income (0.60, 0.52–0.70) were all linked to a reduced risk of poor oral hygiene practices (all p < 0.05).
Table 4 Multivariable ORs and 95% CIs for the Association Between Hand and Oral Hygiene Practices and Sociodemographic Factors (n=26,101)
Associated Factors of Poor Hand Hygiene PracticesTable 4 further shows that the adolescents aged 14–15 years (1.28, 1.16–1.41) and those 16 years or older (1.46, 1.26–1.69), being a girl (1.55, 1.46–1.65), attending an academic high school (1.74, 1.52–2.01) or vocational high school (1.26, 1.10–1.45), having parents with other marital status (divorced, widowed, separated) (1.13, 1.03–1.24), and those living in school dormitories (1.30, 1.22–1.39) were all linked to an increased risk of poor hand hygiene before meals. In contrast, adolescents from high/very high-income families (0.73, 0.62–0.86) were less likely to have poor hand hygiene before meals. Regarding poor hand hygiene after using the toilet, being an only child (1.10, 1.04–1.17) was a risk factor, while attending an academic high school (0.51, 0.45–0.58) and belonging to a middle-income (0.76, 0.67–0.85) or high/very high-income family (0.73,0.63–0.86) were protective. Moreover, the adolescents aged 14–15 years (1.38, 1.24–1.53) and those 16 years or older (1.46, 1.24–1.70), being a girl (1.42, 1.33–1.52), attending an academic high school (1.71, 1.47–1.99), and those living in dormitories (1.61, 1.49–1.73) were linked to an increased risk of poor hand hygiene with using soap. Conversely, adolescents whose fathers (0.83, 0.74–0.93) or mothers (0.88, 0.78–0.98) had a college or higher education, and those from high/very high-income families (0.70, 0.59–0.83) were less likely to exhibit poor hand hygiene with using soap (all p < 0.05).
DiscussionOur study offers the latest evaluation of oral and hand hygiene practices among adolescent students in Zhejiang Province during the COVID-19 pandemic, providing crucial insights into the prevalence and influencing factors of poor hygiene behaviors in this population. The prevalence of poor oral hygiene practice was 29.25%. This rate is higher than that observed in adolescents from 4 Southeast Asian countries (India, Indonesia, Myanmar, and Thailand) (22.4%), 12 Malaysia (12.9%),11 9 African countries (Botswana, Kenya, Namibia, Senegal, Swaziland, Tanzania, Uganda, Zambia, and Zimbabwe) (22.7%), 17 and France (23.9%). 18 However, it is lower compared to Chinese adolescents in 2003 (55.6%), 15 adolescents in Bangladesh (36.4%),10 school adolescents in Southern India (38.1%), 19 and those in Finland, Belgium, and Lithuania (34.9–49.2%). 18 In terms of hand hygiene before meals, the prevalence was 78.06%, which is higher than in the Trinidad and Tobago, Suriname and Dominican Republic (68.2%), 20 6 Southeast Asian countries (Bangladesh, Indonesia, Laos, Philippines, Thailand, and Timor-Leste) (44.8%),10 4 Southeast Asian countries (India, Indonesia, Myanmar, and Thailand) (45.2%),12 Pacific island states (30–35%), 21 9 African countries (Botswana, Kenya, Namibia, Senegal, Swaziland, Tanzania, Uganda, Zambia, and Zimbabwe) (37.8%),17 and global data (43.3%). 22 Poor hand hygiene after using the toilet was 24.67%, similar to that in 4 Southeast Asian countries (India, Indonesia, Myanmar, and Thailand) (26.5%), 12 but lower compared to global data (31.7%), 22 6 Southeast Asian countries (Bangladesh, Indonesia, Laos, Philippines, Thailand, and Timor-Leste)(31.9%),10 and 9 African countries (Botswana, Kenya, Namibia, Senegal, Swaziland, Tanzania, Uganda, Zambia, and Zimbabwe) (41.6%). 17 The prevalence of poor hand hygiene with using soap was 82.56%, higher than in Thailand (73.4%),10 9 African countries (Botswana, Kenya, Namibia, Senegal, Swaziland, Tanzania, Uganda, Zambia, and Zimbabwe) (65.0%),17 6 Southeast Asian countries (Bangladesh, Indonesia, Laos, Philippines, Thailand, and Timor-Leste) (55.8%) 10 and global data (54.7%).22 These findings indicate that poor hand and oral hygiene practices are alarmingly prevalent among adolescent students in Zhejiang Province, Eastern China.
The low percentage of adolescents reporting handwashing after toilet use is concerning and may be attributed to several factors. First, some school restrooms may lack essential supplies, such as paper towels for drying hands, which may discourage students from washing their hands properly. Second, the absence or inconsistent replenishment of soap in school facilities further hinders effective hand hygiene practices. Third, the short duration of breaks between classes may lead students to prioritize other activities over handwashing, as they may perceive it as time-consuming or unnecessary. Additionally, schools often fail to emphasize the importance of handwashing after toilet use through educational campaigns or reminders, which could contribute to a lack of awareness and motivation among students. Addressing these barriers through improved infrastructure, consistent provision of hygiene supplies, targeted educational initiatives, and increased awareness campaigns could help promote better hygiene practices among adolescents.
The multivariable analysis showed that several factors were significantly linked to poor hand and oral hygiene practices. Gender emerged as a significant influence on hygiene behaviors. 18 This study confirmed previous findings10, 18, 23–26 that boys are more likely to exhibit poor oral hygiene compared to girls. However, our study revealed a positive association between girls and poor hand hygiene, which contrasts with other studies.25, 26 Notably, higher family income appeared to serve as a protective factor for both oral and hand hygiene practices, aligning with other study.21 This suggests that financial resources may enhance access to hygiene products and education, which could explain the lower prevalence of proper hand hygiene in lower-income countries due to limited resources and knowledge. Additionally, even in more affluent countries, people from lower socioeconomic backgrounds are more likely to experience poor hygiene and face higher infection risks. 27 Consistent with Schwendicke et al28 our study found that adolescents with higher levels of parental education tend to have better oral hygiene practices. As parents are pivotal in forming children’s hygiene habits, those from lower socioeconomic backgrounds generally display poorer oral hygiene. 29, 30 This is supported by research showing that parents with higher educational levels and incomes are more knowledgeable about preventive dental care programs. 31 Furthermore, our study noted that being an only child correlated with better oral hygiene, consistent with Liu’s findings that only children often have better oral health. 32
Our findings also indicate that adolescents with divorced, widowed, or separated parents, and those residing in school dormitories, face a higher risk of poor hygiene practices. This underscores the importance of family stability and parental supervision in fostering healthy behaviors. Additionally, older adolescents were found to have poorer hand hygiene practices, a finding not always consistent with other researches.11,33 This disparity may be attributed to increased independence and reduced supervision, leading to neglect or shortcuts in hygiene routines. Higher academic pressures could also diminish their focus on personal hygiene.
Cultural factors may play a significant role in shaping both oral and hand hygiene practices.34–36 In some Chinese households, there is a belief that nighttime brushing is more effective in removing accumulated plaque and food debris from the day, thereby preventing dental issues. This cultural preference may lead to neglect of morning brushing, especially among students who face early school start times. Many students struggle to wake up early and often rush through their morning routines, leaving little time for brushing their teeth after breakfast.
Regarding hand hygiene, traditional Chinese cultural attitudes may also influence behaviors.37 A Chinese proverb, “little dirt, never hurt”, may reflect a lack of urgency or awareness about the risks of poor hand hygiene, particularly in informal or non-critical settings. Such cultural beliefs, combined with limited access to handwashing facilities and insufficient education, may explain the low prevalence of handwashing after toilet use or before meals.
This study is crucial for drawing attention to the troubling state of oral and hand hygiene behaviors among adolescent students in Zhejiang Province, Eastern China. It also identifies key high-risk groups and factors that influence hygiene behaviors in this population. The insights gained can guide public health strategies aimed at improving hygiene behaviors among adolescents. By understanding the underlying factors contributing to poor hygiene, targeted educational programs and policies can be developed to promote healthier behaviors among adolescents.
Understanding the limitations inherent in our study is essential. First, due to the cross-sectional nature of the study, establishing causal relationships between the identified factors and hygiene practices is not feasible. Second, the reliance on self-reported data may introduce reporting bias, as participants might underreport or overreport their hygiene behaviors. Lastly, since the research was carried out in a specific region of China, the results may not be applicable to other regions or populations.
ConclusionIn conclusion, adolescent students in Zhejiang Province, Eastern China, exhibit a notably high prevalence of poor oral and hand hygiene practices. Despite increased awareness of hygiene due to the COVID-19 pandemic, a significant portion of adolescents still engage in sub-optimal hygiene practices. This highlights the urgent need to motivate and empower adolescents to take greater responsibility for their personal hygiene. Furthermore, these results emphasize the importance of improving existing oral and hand hygiene promotion programs by incorporating sociodemographic considerations. This study provides valuable baseline data that can inform future research and public health interventions aimed at improving adolescent students’ hygiene practices.
AcknowledgmentsXiangyu Chen and Feng Lu are co-correspondence authors for this study. We would like to express our gratitude to the local CDC staff at each survey site involved in this study.
DisclosureThe authors report no conflicts of interest in this work.
References1. Water MC. Sanitation and hygiene (WASH) in schools in low-income countries: a review of evidence of impact. Int J Environ Res Public Health. 2019;16(3). PubMed: 30696023. doi:10.3390/ijerph16030359
2. Guo D, Shi Z, Luo Y, Ding R, He P. Association between oral health behavior and chronic diseases among middle-aged and older adults in Beijing, China. Bmc Oral Health. 2023;23(1):97. PubMed: 36788510. doi:10.1186/s12903-023-02764-y
3. Beale S, Johnson AM, Zambon M, Hayward AC, Fragaszy EB. Hand hygiene practices and the risk of human coronavirus infections in a UK community cohort. Wellcome Open Res. 2020;5:98. PubMed: 34250260. doi:10.12688/wellcomeopenres.15796.2
4. Aledort JE, Lurie N, Wasserman J, Bozzette SA. Non-pharmaceutical public health interventions for pandemic influenza: an evaluation of the evidence base. Bmc Public Health. 2007;7:208. PubMed: 17697389. doi:10.1186/1471-2458-7-208
5. Stebbins S, Downs JS, Vukotich CJ. Using nonpharmaceutical interventions to prevent influenza transmission in elementary school children: parent and teacher perspectives. J Public Health Man. 2009;15(2):112–117. PubMed: 19202410doi: 10.1097/01.PHH.0000346007.66898.67
6. Gizaw Z, Demissie NG, Gebrehiwot M, Bitew BD, Nigusie A. Oral hygiene practices and associated factors among rural communities in northwest Ethiopia. Bmc Oral Health. 2024;24(1):315. PubMed: 38461252. doi:10.1186/s12903-024-04049-4
7. Toth S, Singer SR, Jiang SS, et al. Associations between periodontal disease severity and selected cardiometabolic risk factors. Quintessence Int. 2024. PubMed: 39352377. doi:10.3290/j.qi.b5768586
8. Agnese C, Schoffer C, Kantorski KZ, Zanatta FB, Susin C, Antoniazzi RP. Periodontitis and oral health-related quality of life: a systematic review and meta-analysis. J Clin Periodontol. 2024. PubMed: 39343995. doi:10.1111/jcpe.14074
9. Braveman P, Gottlieb L. The social determinants of health: it’s time to consider the causes of the causes. Public Health Rep. 2014;129(Suppl 2):19–31. PubMed: 24385661. doi:10.1177/00333549141291S206
10. Pengpid S, Peltzer K. Prevalence and associated factors of oral and hand hygiene behaviour among adolescents in six Southeast Asian countries. Int J Adolesc Med Health. 2020;33(6):421–427. PubMed: 32549158. doi:10.1515/ijamh-2019-0177
11. Che SN, Mohamad AM, Abdullah NA, et al. Prevalence and factors associated with oral and hand hygiene practices among adolescents in Malaysia: findings from the national health and morbidity survey 2017. Asia-Pac J Public Health. 2019;31(8_suppl):97S–104S. PubMed: 31640393. doi:10.1177/1010539519880998
12. Peltzer K, Pengpid S. Oral and hand hygiene behaviour and risk factors among in-school adolescents in four Southeast Asian countries. Int J Environ Res Public Health. 2014;11(3):2780–2792. PubMed: 24608901. doi:10.3390/ijerph110302780
13. Mehta A, Kaur G. Oral health-related knowledge, attitude, and practices among 12-year-old schoolchildren studying in rural areas of Panchkula, India. Indian J Dent Res. 2012;23(2):293. PubMed: 22945729. doi:10.4103/0970-9290.100446
14. Wang M, Xu J, Fang H, et al. Associations of weight control related behaviors with current cigarette smoking among Chinese adolescents: results from an ongoing school-based survey in Zhejiang province. Tob Induc Dis. 2024:22. PubMed: 39280935. doi:10.18332/tid/192001
15. Zhu L, Petersen PE, Wang H-Y, Bian J-Y, Zhang B-X. Oral health knowledge, attitudes and behaviour of children and adolescents in China. Int Dent J. 2003;53(5):289–298. PubMed: 14560803. doi:10.1111/j.1875-595x.2003.tb00762.x
16. Kokka I, Mourikis I, Nicolaides NC, et al. Exploring the effects of problematic internet use on adolescent sleep: a systematic review. Int J Environ Res Public Health. 2021;18(2):760. PubMed: 33477410. doi:10.3390/ijerph18020760
17. Pengpid S, Peltzer K. Hygiene behaviour and associated factors among in-school adolescents in nine African countries. Int J Behav Med. 2011;18(2):150–159. PubMed: 20593258. doi:10.1007/s12529-010-9109-6
18. Zaborskis A, Kavaliauskiene A, Levi S, Tesler R, Dimitrova E. Adolescent toothbrushing and its association with sociodemographic factors-time trends from 1994 to 2018 in twenty countries. Healthcare-Basel. 2023;11(24). PubMed: 38132038. doi:10.3390/healthcare11243148
19. Gupta T, Sequeira P, Acharya S. Oral health knowledge, attitude and practices of a 15-year-old adolescent population in Southern India and their social determinants. Oral Health Prev Dent. 2012;10(4):345–354. PubMed: 23301235.
20. Pengpid S, Peltzer K. Hand and oral hygiene practices among adolescents in Dominican Republic, Suriname and Trinidad and Tobago: prevalence, health, risk behavior, mental health and protective factors. Int J Environ Res Public Health. 2020;17(21). PubMed: 33120963. doi:10.3390/ijerph17217860
21. Tran D, Phongsavan P, Bauman AE, Havea D, Galea G. Hygiene behaviour of adolescents in the Pacific: associations with socio-demographic, health behaviour and school environment. Asia-Pac J Public Health. 2006;18(2):3–11. PubMed: 16883964. doi:10.1177/10105395060180020201.
22. Jatrana S, Hasan MM, Mamun AA, Fatima Y. Global variation in hand hygiene practices among adolescents: the role of family and school-level factors. Int J Environ Res Public Health. 2021;18(9). PubMed: 34067142. doi:10.3390/ijerph18094984
23. Sadinejad M, Kelishadi R, Qorbani M, et al. A Nationwide Survey on Some Hygienic Behaviors of Iranian Children and Adolescents: the CASPIAN-IV Study. Int J Preventive Med. 2014;5(9):1083–1090. PubMed: 25317289.
24. Nordhauser J, Rosenfeld J. Adapting a water, sanitation, and hygiene picture-based curriculum in the Dominican Republic. Glob Health Promot. 2020;27(3):6–14. PubMed: 31736435. doi:10.1177/1757975919848111
25. Dobe M, Mandal RN, Jha A. Social determinants of good hand-washing practice (GHP) among adolescents in a rural Indian community. Fam Community Health. 2013;36(2):172–177. PubMed: 23455687. doi:10.1097/FCH.0b013e318282ac42
26. Park Y-D, Patton LL, Kim H-Y. Clustering of oral and general health risk behaviors in Korean adolescents: a national representative sample. J Adolescent Health. 2010;47(3):277–281. PubMed: 20708567. doi:10.1016/j.jadohealth.2010.02.003
27. Smith L, Butler L, Tully MA, et al. Hand-washing practices among adolescents aged 12-15 years from 80 countries. Int J Environ Res Public Health. 2020;18(1):PubMed: 33375506. doi:10.3390/ijerph18010138
28. Schwendicke F, Dörfer CE, Schlattmann P, Page LF, Thomson WM, Paris S. Socioeconomic inequality and caries: a systematic review and meta-analysis. J Dent Res. 2015;94(1):10–18. PubMed: 25394849. doi:10.1177/0022034514557546
29. Ayele FA, Taye BW, Ayele TA, Gelaye KA. Predictors of dental caries among children 7-14 years old in Northwest Ethiopia: a community based cross-sectional study. Bmc Oral Health. 2013;13:7. PubMed: 23331467. doi:10.1186/1472-6831-13-7
30. Peres MA, Peres KG, de Barros AJD, Victora CG. The relation between family socioeconomic trajectories from childhood to adolescence and dental caries and associated oral behaviours. J Epidemiol Commun H. 2007;61(2):141–145. PubMed: 17234873. doi:10.1136/jech.2005.044818
31. Saldunaite K, Bendoraitiene EA, Slabsinskiene E, Vasiliauskiene I, Andruskeviciene V, Zubiene J. The role of parental education and socioeconomic status in dental caries prevention among Lithuanian children. Medicina-Lithuania. 2014;50(3):156–161. PubMed: 25323543doi: 10.1016/j.medici.2014.07.003
32. Liu M, Yun Q, Zhao M, et al. Association of siblings’ presence and oral health-related quality of life among children: a cross-sectional study. Bmc Oral Health. 2021;21(1):153. PubMed: 33757508. doi:10.1186/s12903-021-01526-y
33. Seidu A, Amu H, Salihu T, et al. Prevalence and factors associated with hygiene behaviours among in-school adolescents in Ghana. J. 2021;4(2):169–181. doi:10.3390/j4020014
34. Butani Y, Weintraub JA, Barker JC. Oral health-related cultural beliefs for four racial/ethnic groups: assessment of the literature. Bmc Oral Health. 2008;8:26. PubMed: 18793438. doi:10.1186/1472-6831-8-26
35. Ruslana FH, Mulyono S. The relationship of cultural values with clean and healthy life behaviour (CHLB) among Islamic boarding school students in Indonesia. J Public Health Res. 2021;11(2):PubMed:35255670. doi:10.4081/jphr.2021.2739
36. Wong D, Perez-Spiess S, Julliard K. Attitudes of Chinese parents toward the oral health of their children with caries: a qualitative study. Pediatr Dent. 2005;27(6):505–512. PubMed: 16532893.
37. Tao SY, Cheng YL, Lu Y, Hu YH, Chen DF. Handwashing behaviour among Chinese adults: a cross-sectional study in five provinces. Public Health. 2013;127(7):620–628. PubMed: 23790806. doi:10.1016/j.puhe.2013.03.005
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