Introduction
Oral well-being is an essential part of overall health, and preventive measures are crucial in reducing the risks associated with harmful oral habits. Risky oral habits such as smoking and betel quid chewing are major factors contributing to oral health problems, including an increased risk of oral cancer and related diseases.
Oral cancer is one of the most dangerous diseases among all oral conditions, caused by the abnormal growth of cells in the oral cavity. Several factors contribute to the development of oral cancer, including smoking, betel quid chewing, alcohol consumption, chronic inflammation, genetics, and immunodeficiency. Treatment options for oral cancer include surgery, radiation therapy, chemotherapy, or a combination of these methods. The success rate of treatment decreases with the progression of the disease, so early detection of oral cancer and the avoidance of risk habits are essential [1–16].
Oral cancer screening programs can significantly reduce mortality rates by enabling early detection of oral cancer and oral potentially malignant disorders (OPMDs), allowing timely referral for appropriate treatment [17–19]. These screening programs recognize the importance of early detection and intervention, making them a vital tool for promoting oral health awareness and encouraging habit change [20]. Participants in such screening programs are expected to modify their habits appropriately to reduce their risk of developing oral diseases in the future.
Previous research, whether based on surveys or cohort databases, suggests that factors such as dosage of consumption, educational level, illness, and intention to adjust habits have an impact on the likelihood of success in promoting positive changes in tobacco and betel quid chewing habits. Nevertheless, these investigations are limited to enhancing a single harmful habit, such as smoking or betel quid chewing [21–27]. However, in reality, most individuals with oral risk habits do not engage in just one single risky habit, as these habits can often trigger or reinforce the development of other associated risk habits [28].
This study aims to report the changes in oral risk habits among individuals participating in an oral screening program that targeted those engaged in high-risk oral habits, including cigarette smoking and betel quid chewing. We also investigated factors associated with changes in oral habits, yielding more precise insights into the consequences of harmful modifications. The primary objective of this study is to investigate the changes in oral risk habits and assess the factors linked to the adoption of advantageous oral habits among individuals participating in a population-based oral cancer screening program in Taiwan. This analysis will consider combining two specific oral risk habits, cigarette smoking and betel quid chewing.
Materials and methods
Study design and setting
This is a retrospective cohort study that uses data from the oral cancer screening program in Taiwan.
Data source and collection
This study utilized data collected between 2010 and 2021 from a population-based oral cancer screening program. Individuals aged 18 and above who smoke or chew betel quid are voluntarily invited to attend the biennial screening program, which is reimbursed by the Health Promotion Administration (HPA). All screening procedures were conducted at local clinics and hospitals. Oral examinations were performed by dentists, otolaryngologists, and other specialists who had completed a training program provided by HPA. This training, conducted by certified oral surgeons and senior dentists, lasted approximately three days and included both theoretical instruction and practical assessments. The program was specifically designed to enhance the detection of suspicious oral mucosal lesions. Suspected cases identified during the screenings were referred to hospital specialists for confirmatory pathological diagnosis. A screening data monitoring and surveillance center recorded screening, referral, and diagnosis data. Demographic information, oral habits, and screening results were collected at each visit. A structured questionnaire was used to gather demographic data and information on cigarette smoking and betel quid chewing through face-to-face interviews conducted in community and hospital settings [19]. Trained dentists or physicians conducted visual examinations of participants’ oral cavities to identify Oral Potentially Malignant Disorders (OPMDs), including oral leukoplakia, erythroleukoplakia, erythroplakia, oral submucous fibrosis, and verrucous hyperplasia. Chuang (2017) outlined the coding issues and specifics of this screening program [19]. Health education, including information on risk factors, risky behaviors, and proper oral hygiene practices, was provided immediately after the screening. Each session typically lasted 10–15 minutes per participant and included verbal counseling along with visual aids such as pamphlets and posters. Public health nurses and trained educators delivered the education under the supervision of dental professionals.
It is recognized that interview-based data collection is prone to biases, including interviewer bias, social desirability bias, and recall bias. To minimize these biases, all interviews were conducted by trained professionals as mentioned above. For study purposes, data from January 2010 to December 2021 were accessed on November 22, 2022. Information that could identify individual participants during or after data collection was accessible only to Dr. Amy Ming-Fang Yen, the co-principal investigator of the National Oral Cancer Screening Surveillance Program. The aggregated dataset used in this study has been publicly uploaded to the Dryad repository and is available at: https://doi.org/10.5061/dryad.612jm64h3.
Participants and variables
This study includes all screening records that met specific criteria: participants aged over 30 who attended the oral cancer screening program in Taiwan at least twice between 2010 and 2021. Based on findings from a previous study indicating that individuals under the age of 30 have a very low risk of malignancy, this study set the inclusion criterion at age over 30 [20]. After excluding 10,853 individuals under the age of 30, data from approximately 2.6 million participants were included in the analysis. The dataset contains information on oral habit changes, age groups (30–45, 46–60, 60+), sex, education level (elementary school, middle and high school, college or higher), screening frequency (only twice, more than twice), and oral potentially malignant disorders (OPMDs) status (positive or negative findings). As part of the screening program, oral cancer risk and prevention education were provided, and changes in oral habits were recorded at each screening to evaluate the effectiveness of the educational component.
Measurement of cigarette smoking and betel quid chewing
This study intends to investigate two habits, cigarette smoking and betel quid chewing. This study used 10 years of use and 20 pieces per day as the criteria for classifying levels of oral habits, based on previous studies [29,30]. The use of cigarette smoking is categorized into 3 levels: LS: never smoke, cessation, and low degree (<10 years and <20 pieces per day); MS: medium degree (<10 years and ≥20 pieces per day, ≥ 10 years and < 20 pieces per day); and HS: high degree (≥10 years and ≥20 pieces per day). The betel quid chewing is categorized into 5 levels NB: never chewing, QB: cessation, LB: low degree (<10 years and <20 pieces per day), MB: medium degree (<10 years and ≥20 pieces per day, ≥ 10 years and < 20 pieces per day), and HB: high degree (≥10 years and ≥20 pieces per day). The combined oral habit changes between the first and the last screening for cigarette smoking and betel quid chewing were rated to improve and not improve (Fig 1a). The improvement of the combination of smoking and betel quid chewing indicates that at least 1 habit is being improved with no other habit worsening (Fig 1d). The improvement of smoking and betel quid chewing was defined as shown in Fig 1b, c.
[Figure omitted. See PDF.]
(A.) Participants who attended at least two screening visits were included in this study. Oral habit changes were compared between the first and last screening visits, regardless of the total number of visits, if more than two were attended. (B.) The improving oral habit changes of betel quid chewing. (C.) The improving oral habit changes of smoking. (D.) The improvement of combined oral habit changes between cigarette smoking and betel quid chewing indicates that at least 1 habit has to be improved, with no other habit getting worse. Oral habits: NB-never chewing betel quid, QB-quit the chewing, LB-low degree chewing, MB-medium degree chewing, HB-high degree chewing, LS-never or quit or low degree smoking, MS-medium degree smoking, and HS-high degree smoking.
Statistical analysis
The oral habit changes (improved, no change, or deterioration) were summarized as numbers and percentages by the following characteristics: oral habits of the first screening, sex, age, education, screening times, and OPMD screening results. The investigation of the associated factors for improving habit changes was established with the logistic regression model and 95% confidence intervals (Wald method). The key assumptions for logistic regression were met, including independence of observations, a binary outcome, and absence of multicollinearity. The data were collected from independent observation, and all variables showed acceptable variance inflation factor (VIF) values (<2), indicating no serious multicollinearity. The outcome of the model was improvement or non-improvement. For missing data, this study categorized it as one level of the data, allowing for adjustments during the analysis. Note that individuals in LS and also in QB/LB at baseline were not included in the logistic regression analysis because they did not have a space to improve. All analyses were conducted with SAS version 9.4 (SAS Institute, Cary, NC, USA).
Ethical considerations
The Research Ethics Committee of the National Taiwan University Hospital approved this study under the annual Institutional Review Board (IRB) approval process and waived the requirement for informed consent in accordance with institutional review board regulations. This study was conducted from 2022 to 2024 under ethical approval numbers 202204036W, 202306056W, and 202403087W for each respective year. The study protocol was reviewed and approved by the Health Promotion Administration of the Taiwanese government, adhering to the ethical principles of the Declaration of Helsinki and its amendments.
Results
Oral habit changes distribution
There were 2,569,920 participants aged 30 years and older had at least two times of screening between 2010 and 2021. Among the participants who underwent repeated screening, 25.3% made a change to improve their oral habits. For those never chewed betel quids, participants with medium-degree and high-degree smoking changed to improving habits by 8.8% and 33.1%, respectively. Participants stopped chewing betel quids with medium-degree smoking, and high-degree smoking changed to improve habits by 24.1% and 46.1%, respectively. Low-degree chewing betel quids with no smoking, low-degree smoking, medium-degree smoking, and high-degree smoking all improved to 34.4%, 52.8%, and 69.9%, respectively. Medium-degree chewing betel quids with no smoking, low-degree smoking, medium-degree smoking, and high-degree smoking improved to 42.3%, 53.3%, and 74.2%, respectively. High-degree chewing betel quids with no smoking, low-degree smoking, medium-degree smoking, and high-degree smoking improved to 48.7%, 55.9%, and 72.7%, respectively. Males changed to improving habits at 26.2%, while females were at 20.8%. Participants aged 30–45 years, 46–60 years, and over 61 years changed to improving habits at 25.2%, 26.8%, and 23%, respectively. Among participants, 25.5% of those whose highest education level was elementary school demonstrated habit improvement, compared to 26.7% of those with education up to middle school or high school, and 22.6% of those with education beyond college. Among participants, 35.9% of those with a positive OPMD screening result showed habit improvement, compared to 24.5% in the negative screening group. Regarding participation frequency, 23.7% of those who participated only twice and 27.1% of those who participated more than twice in the oral screening program demonstrated habit improvement Table 1.
[Figure omitted. See PDF.]
S1 Table in S1 File shows medium-degree betel quid chewing with high-degree smoking (MBHS) and high-degree betel quid chewing with high-degree smoking (HBHS) in males could improve habits by more than 70%, while low-degree betel quid chewing with high-degree smoking (LBHS), medium-degree betel quid chewing with high-degree smoking (MBHS), and high-degree betel quid chewing with high-degree smoking (HBHS) in females could improve habits by more than 70%. Positive OPMDs who engaged in medium-degree betel quid chewing with high-degree smoking (MBHS) and high-degree betel quid chewing with high-degree smoking (HBHS) saw an improvement in their habits of more than 70%. On the other hand, when the negative group engaged in low-degree betel quid chewing with high-degree smoking (LBHS), medium-degree betel quid chewing with high-degree smoking (MBHS), and high-degree betel quid chewing with high-degree smoking (HBHS), their habits improved by more than 70%. Improving habits more than 70% found in medium-degree betel quid chewing with high-degree smoking (MBHS) of aged 30–45 years; low-degree betel quid chewing with high-degree smoking (LBHS), medium-degree betel quid chewing with high-degree smoking (MBHS), and high-degree betel quid chewing with high-degree smoking (HBHS) of aged 46–60 years; low-degree betel quid chewing with smoking over medium-degree level (LBMS LBHS), medium-degree betel quid chewing with high-degree smoking (MBHS) and high-degree smoking with smoking over medium-degree level (HBMS HBHS) of aged over 61 years. Improving habit of more than 70% was found in low-degree betel quid chewing with high-degree smoking (LBHS), medium-degree betel quid chewing with high-degree smoking (MBHS) and high-degree betel quid chewing with high-degree smoking (HBHS) of participants whose highest education was elementary school; medium-degree betel quid chewing with high-degree smoking (MBHS) and high-degree betel quid chewing with high-degree smoking (HBHS) of participants whose highest education was middle and high school; low-degree betel quid chewing with high-degree smoking (LBHS), medium-degree betel quid chewing with high-degree smoking (MBHS) and high-degree betel quid chewing with high-degree smoking (HBHS) of participants whose highest education level was over college. Two-time screening participation resulted in an improvement of more than 70% in medium-degree betel quid chewing with high-degree smoking (MBHS); on the other hand, more than two-time screening participation led to an improvement of more than 70% in low-degree betel quid chewing with high-degree smoking (LBHS), medium-degree betel quid chewing with high-degree smoking (MBHS), and high-degree betel quid chewing with high-degree smoking (HBHS) S1 Table in S1 File.
Factors related to better habit changes
This logistic regression model was adjusted for age group, sex, education level, oral habit severity, screening frequency, and initial OPMD diagnosis. To simplify the categorization of oral habits severity during the first round of screenings, we consolidate them into four distinct groups: only cigarette smoking, betel quid chewing combined with mild smoking, betel quid chewing combined with moderate smoking, and betel quid chewing combined with severe smoking. This approach helps to avoid an excessive number of levels. The study revealed that the favorable results of OPMDS had a significant impact on improving habits, but only in people who had a smoking habit exclusively (adjusted odds ratio (aOR) 1.18, 95% confidence interval (CI) 1.16–1.20). However, the presence of OPMD did not lead to improvement in habits for individuals who engaged in both smoking and chewing betel quids (aOR 0.84 (95% CI 0.82–0.87) for individuals who chewed betel quid and engaged in mild smoking, aOR 0.79 (95% CI 0.77–0.81) for those who chewed Betel quid and engaged in moderate smoking, aOR 0.88 (95% CI 0.86–0.9) for those who chewed betel quid and engaged in severe smoking). Males were less likely to improve their oral habits compared to females (aOR = 0.86, 95% CI: 0.85–0.87). Compared to individuals aged 30−45 years, it demonstrated that as age increased, there was a significant increase in improving oral habit. The adjusted odds ratio (95% confidence interval) was 1.31 (1.3–1.32) for individuals aged 46–60 years and 1.71 (1.69–1.73) for those over 61 years. Those with the highest education level in middle and high school showed a decreased likelihood of habit improvement when comparing their education to the elementary school level (aOR 0.94, 95% CI 0.93–0.95), while individuals with the highest level of education beyond college have a greater chance of improving their habits (aOR 1.09, 95% CI 1.08–1.11). Participating attending more than two rounds of screening, compared to two rounds of screening, significantly increased the opportunity for habit improvement (aOR 1.046, 95% CI 1.038–1.053) Table 2.
[Figure omitted. See PDF.]
Discussion
Among participants who had never chewed betel quid, those with low degree smoking habits were more likely to exhibit worsening habits (75.8%) compared to those with higher degree smoking habits. In contrast, individuals who had previously quit betel quid chewing, indicating they had already modified at least one risky habit, showed less deterioration in low-degree smoking habits (33.5%). This suggests that smoking habits are more prone to worsening than betel quid chewing, which is consistent with previous findings [31]. Moreover, when focusing on the group with high-degree smoking habits, it was found that individuals who also engaged in betel quid chewing demonstrated greater improvement in their habits. This suggests that betel quid chewing may have a stronger influence on habit modification than smoking. US and Korean populations’ studies showed that people with high-degree smoking decreased the opportunity for improving oral risk habits (smoking cessation), with an OR (95% CI) of 0.42 (0.35, 0.5) and 0.67 (0.47, 0.95), respectively [25,26]. It is possible that the easier accessibility of cigarettes nowadays, for example, their availability in convenience stores, may contribute to the difficulty in improving smoking behavior.
Those diagnosed with OPMDs can increase health awareness and promote habit modification among cigarette smokers (aOR 1.18, 95%CI: 1.16–2). The study in China and Korea, which found that participant illness influenced smoking improvement [26,32], supports this result. According to a study in China, illness was the 47.3% most common reason for smoking cessation [32]. In Korea, a study found that illness affected smoking cessation with an OR (95% CI) of 1.4 (1.07, 1.85) for hypertension and 1.68 (1.03, 2.75) for cardiovascular disease [26]. Some suspected abnormal findings on CT screening affected smoking’s improvement [33,34]. Although the presence of OPMD may help motivate habit change among individuals with only a smoking habit (low-risk group), its effect appears limited among those with both smoking and betel quid chewing habits (high-risk group). This is despite the high-risk group demonstrating a higher proportion of habit improvement. These findings suggest that awareness of the dangers associated with OPMD may still be insufficient. Therefore, enhancing the effectiveness of oral cancer screening programs may require the integration of targeted strategies aimed at increasing participants’ understanding of the severity and long-term consequences of OPMDs.
Male individuals demonstrated a greater capacity for enhancing their habits in comparison to their female counterparts. However, consideration of other variables revealed that males showed less improvement in their habits than females (aOR 0.86, 95%CI: 0.85–0.87). Previous research conducted in the US and China also found that men were less likely to quit smoking, with adjusted odds ratios (aOR) of 0.96 (95% CI: 0.84–1.11) in the US [25] and 0.81 (95% CI: 0.43–1.54) in China [27]. Conversely, the Malaysian study found a hazard rate ratio (HRR) of 0.82 for females who stopped chewing betel quid, with a 95% confidence interval spanning from 0.5 to 1.3 [21]. Nevertheless, the outcomes of all three trials did not demonstrate statistical significance. In China, further research showed a similar distribution, with 16.6% of males and 16.3% of females intending to quit smoking [32]. Evidence indicates that both males and females can contribute to habit enhancement, with differing effects depending on geographical area.
The opportunity for improving the oral risk habits of both models in this study is higher as age increases (aOR 1.31, 95%CI:1.3–1.32 for age 46−60 and aOR 1.71, 95%CI:1.69–1.73). However, researchers found that elderly Malaysians were less likely to stop their betel quid chewing habit (HRR 0.2, 95% CI 0.1–0.6) [21]. Additionally, some studies of smoking cessation in China and Korea showed a non-significant effect of age, with an OR (95% CI) of 0.94 (0.4, 2.23) and 2.35 (0.48, 11.45), respectively [24,27]. The disparities in oral health outcomes among regions can be attributed to differences in health awareness and adherence to traditional practices. Nevertheless, it is encouraging to see that middle-aged and older adults in Taiwan are becoming more attentive to their oral health. Even greater benefits, however, could be realized if the avoidance of risky behaviors were instilled from a younger age.
The participants’ highest level of education, particularly a college degree or higher, can positively influence habit improvement (aOR 1.09, 95%CI: 1.08–1.11). The findings of this study align with prior research conducted in China and Korea. In China, a study found that education has a non-significant effect on improving cigarette smoking, with an OR (95% CI) of 1.21 (0.84, 1.74) for medium education and 1.29 (0.83, 1.98) for high education, compared to low education [27]. However, this survey study in China was limited to urban areas, but most Chinese smokers live in rural areas [27]. The study in Korea showed that higher education increases the opportunity for improving cigarette smoking, with an OR (95% CI) of 3.19 (1.02, 9.98) [24]. Highly educated persons sometimes prioritize their personal opinions over societal conventions. Once individuals comprehensively grasp the risks linked to their behaviors, they are more inclined to implement modifications.
Conducting screenings more than twice could improve participants’ habits (aOR 1.046, 95%CI: 1.038–1.053). Repeated participation indicates a deliberate effort to change these oral risky habits and maintain a healthy lifestyle. Other studies in China and Korea also found the same pattern: participants who intended to quit smoking were more successful [24,26,27]. The study in Korea used the clinic visit period to demonstrate the intention to quit smoking and found the impact to be an OR (95% CI) of 7.16 (5.57, 9.2) [26]. Among Korean participants who consulted about smoking cessation, counseling increased the opportunity for success, with an OR (95% CI) of 1.87 (1.21, 2.89) [24]. Among Chinese participants, those who tried to quit smoking had more improvement in smoking cessation, with an OR (95% CI) of 2.29 (1.81, 2.89) [27]. It is anticipated that increased promotion and public awareness campaigns about the screening program could enhance participation and lead to greater improvements in oral health behaviors.
The investigation reveals that a quarter of the participants in an oral cancer screening program were able to effectively enhance their practices. The screening program offers both early diagnosis of abnormal lesions or diseases and knowledge about oral risk factors that can lead to oral cancer. The study found that individuals who engaged in both betel quid chewing and smoking were more likely to improve their habits than those who smoked only. Oral potentially malignant disorders (OPMDs) are conditions that may progress to oral cancer; thus, detecting such abnormalities should encourage individuals to adopt healthier behaviors. However, the positive impact of OPMD was observed only among participants who smoked but did not chew betel quid, indicating a lack of awareness about the dangers associated with OPMDs. Age-related vulnerability to illness may explain why older adults in this study appeared to have greater awareness of health risks and were more likely to engage in positive habit modification. Additionally, individuals with higher education levels may be more inclined to adhere to their own reasoning rather than societal values. Once they understand the dangers of their personal habits, they are more likely to make informed decisions to change. Regular participation in screening programs also reflects a strong and consistent commitment to personal health, which can foster successful long-term habit improvement. In Taiwan, oral cancer screening programs are conducted by trained oral health professionals, including doctors, nurses, and technicians, which enhances the credibility and effectiveness of the program in promoting healthy behaviors [35–40].
However, 75% of participants did not show improvement in their risk habits, particularly among those with low-intensity habits. It is possible that these individuals perceive low levels of consumption as harmless. If this is the case, increasing the intensity of educational content to emphasize the dangers associated with even low-level use, along with promoting more consistent participation in the screening program, may be necessary to enhance the effectiveness of habit change. Furthermore, other underlying factors may hinder improvement in this group. Future research should consider exploring additional determinants such as socioeconomic constraints and the accessibility of cigarettes and betel quid.
Limitations
Nevertheless, we used participant cognition to gather data on their highest level of education and information about cigarette or betel quid consumption. As a result, the occurrence of recall bias is a very plausible scenario. The current study had one limitation. As we had a particular set of people who participated in the screening program at least twice as the subject of the current study, the results could not be generalized to people who participated in the screening program only once.
Conclusion
This study highlights that 25% of participants improved their oral habits, reflecting a positive outcome of the oral cancer screening program. The most significant improvements were observed among elderly individuals, those with higher education levels, and participants who consistently engaged with the program. These findings underline the potential of such initiatives to foster healthier habits, particularly among groups more likely to be influenced by health education and regular monitoring. However, being diagnosed with oral potentially malignant disorders (OPMDs) has not proven to be a strong motivator for habitual change, except among individuals who smoked but did not engage in other risky habits, such as betel quid chewing. This indicates a gap in awareness among high-risk groups engaging in multiple risky habits, who seem less likely to recognize the dangers of their habits or the severity of OPMDs.
To address this issue, future efforts should focus on enhancing public knowledge and understanding through collaboration between health organizations and the screening program. By promoting greater awareness of the risks associated with smoking, betel quid chewing, and OPMDs, such partnerships could help individuals recognize the importance of changing their habits. Increased understanding could empower individuals to make more informed decisions about their health. Enhancing the effectiveness of the oral cancer screening program could further reduce the incidence of oral cancer over time and significantly lower the healthcare costs associated with its treatment. These combined efforts would not only improve individual outcomes but also strengthen the overall impact of the screening initiative on public health.
Supporting information
S1 File.
S1 Table Characteristics of oral habit change used in the logistic regression model (improve and not improve). S2 Table The number of study participants per number of visits.
https://doi.org/10.1371/journal.pone.0320461.s001
(ZIP)
Acknowledgments
The authors provide their warm thanks and appreciation to all study participants.
References
1. 1. Raghavi S, Anbarasu K. Unravelling the role of key genes in oral cancer progression: a comprehensive review. Oral Oncology Reports. 2024;10:100384.
* View Article
* Google Scholar
2. 2. Canadian Cancer Society. Risk factors for oral cancer. 2024. https://cancer.ca/en/cancer-information/cancer-types/oral/risks
* View Article
* Google Scholar
3. 3. Bagnardi V, Rota M, Botteri E, Tramacere I, Islami F, Fedirko V, et al. Alcohol consumption and site-specific cancer risk: a comprehensive dose-response meta-analysis. Br J Cancer. 2015;112(3):580–93. pmid:25422909
* View Article
* PubMed/NCBI
* Google Scholar
4. 4. Gupta B, Johnson NW. Systematic review and meta-analysis of association of smokeless tobacco and of betel quid without tobacco with incidence of oral cancer in South Asia and the Pacific. PLoS One. 2014;9(11):e113385. pmid:25411778
* View Article
* PubMed/NCBI
* Google Scholar
5. 5. Janbaz KH, Qadir MI, Basser HT, Bokhari TH, Ahmad B. Risk for oral cancer from smokeless tobacco. Contemp Oncol (Pozn). 2014;18(3):160–4. pmid:25520574
* View Article
* PubMed/NCBI
* Google Scholar
6. 6. Anwar N, Pervez S, Chundriger Q, Awan S, Moatter T, Ali TS. Oral cancer: clinicopathological features and associated risk factors in a high risk population presenting to a major tertiary care center in Pakistan. PLoS One. 2020;15(8):e0236359. pmid:32760151
* View Article
* PubMed/NCBI
* Google Scholar
7. 7. Jose M, Rajagopal V, Thankam FG. Chapter 9 - Oral tissue regeneration: Current status and future perspectives. In: Sharma CPBT-RO. Academic Press; 2021: 169–87. https://www.sciencedirect.com/science/article/pii/B9780128210857000099
8. 8. Xiao X, Wang Z. Oral Cancer. Pharynx - Diagnosis and Treatment. IntechOpen; 2021. https://doi.org/10.5772/intechopen.97330
9. 9. Chen Z, Chan ABW, Kam L-S, Chan M-H, Chan JYK, Lee W-T, et al. Changes in the incidence and human papillomavirus-Positive portion of oropharyngeal squamous cell carcinoma in Hong Kong. Cancers (Basel). 2024;16(1):226. pmid:38201653
* View Article
* PubMed/NCBI
* Google Scholar
10. 10. Senevirathna K, Pradeep R, Jayasinghe YA, Jayawickrama SM, Illeperuma R, Warnakulasuriya S, et al. Carcinogenic effects of areca nut and its metabolites: a review of the experimental evidence. Clin Pract. 2023;13(2):326–46. pmid:36961055
* View Article
* PubMed/NCBI
* Google Scholar
11. 11. Tapak L, Ghasemi MK, Afshar S, Mahjub H, Soltanian A, Khotanlou H. Identification of gene profiles related to the development of oral cancer using a deep learning technique. BMC Med Genomics. 2023;16(1):35. pmid:36849997
* View Article
* PubMed/NCBI
* Google Scholar
12. 12. Poell JB, Wils LJ, Brink A, Dietrich R, Krieg C, Velleuer E, et al. Oral cancer prediction by noninvasive genetic screening. Int J Cancer. 2023;152(2):227–38. pmid:36069231
* View Article
* PubMed/NCBI
* Google Scholar
13. 13. Lechner M, Liu J, Masterson L, Fenton TR. HPV-associated oropharyngeal cancer: epidemiology, molecular biology and clinical management. Nat Rev Clin Oncol. 2022;19(5):306–27. pmid:35105976
* View Article
* PubMed/NCBI
* Google Scholar
14. 14. Pérez Jardón A, Arroyo E, Gándara Vila P, Pérez-Sayáns M. Risk factors of oral cancer: identification and mechanism of prevention. Handbook of Cancer and Immunology. Springer International Publishing; 2023: 1–29. https://doi.org/10.1007/978-3-030-80962-1_331-1
15. 15. Aghiorghiesei O, Zanoaga O, Nutu A, Braicu C, Campian RS, Lucaciu O. The world of oral cancer and its risk factors viewed from the aspect of microRNA expression patterns. Genes. 2022;13.
* View Article
* Google Scholar
16. 16. Roman BR, Aragones A. Epidemiology and incidence of HPV-related cancers of the head and neck. J Surg Oncol. 2021;124(6):920–2. pmid:34558067
* View Article
* PubMed/NCBI
* Google Scholar
17. 17. Sankaranarayanan R, Ramadas K, Thara S, Muwonge R, Thomas G, Anju G, et al. Long term effect of visual screening on oral cancer incidence and mortality in a randomized trial in Kerala, India. Oral Oncol. 2013;49(4):314–21. pmid:23265945
* View Article
* PubMed/NCBI
* Google Scholar
18. 18. Rajaraman P, Anderson BO, Basu P, Belinson JL, Cruz AD, Dhillon PK, et al. Recommendations for screening and early detection of common cancers in India. Lancet Oncol. 2015;16(7):e352-61. pmid:26149887
* View Article
* PubMed/NCBI
* Google Scholar
19. 19. Chuang S-L, Su WW-Y, Chen SL-S, Yen AM-F, Wang C-P, Fann JC-Y, et al. Population-based screening program for reducing oral cancer mortality in 2,334,299 Taiwanese cigarette smokers and/or betel quid chewers. Cancer. 2017;123(9):1597–609. pmid:28055109
* View Article
* PubMed/NCBI
* Google Scholar
20. 20. Chuang S-L, Wang C-P, Chen M-K, Su WW-Y, Su C-W, Chen SL-S, et al. Malignant transformation to oral cancer by subtype of oral potentially malignant disorder: a prospective cohort study of Taiwanese nationwide oral cancer screening program. Oral Oncol. 2018;87:58–63. pmid:30527244
* View Article
* PubMed/NCBI
* Google Scholar
21. 21. Ghani WMN, Razak IA, Yang Y-H, Talib NA, Ikeda N, Axell T, et al. Factors affecting commencement and cessation of betel quid chewing behaviour in Malaysian adults. BMC Public Health. 2011;11:82. pmid:21294919
* View Article
* PubMed/NCBI
* Google Scholar
22. 22. Lai C-S, Shieh T-Y, Yang Y-HC, Chong M-Y, Hung H-C, Tsai C-C. Factors associated with quitting areca (betel) quid chewing. Community Dent Oral Epidemiol. 2006;34(6):467–74. pmid:17092276
* View Article
* PubMed/NCBI
* Google Scholar
23. 23. Wang J-H, Yang Y-F, Zhao S-L, Liu H-T, Xiao L, Sun L, et al. Attitudes and influencing factors associated with smoking cessation: An online cross-sectional survey in China. Tob Induc Dis. 2023;21:87. pmid:37377525
* View Article
* PubMed/NCBI
* Google Scholar
24. 24. Yeom H, Lim H-S, Min J, Lee S, Park Y-H. Factors affecting smoking cessation success of heavy smokers registered in the intensive care smoking cessation camp (Data from the National Tobacco Control Center). Osong Public Health Res Perspect. 2018;9(5):240–7. pmid:30402379
* View Article
* PubMed/NCBI
* Google Scholar
25. 25. Fagan P, Augustson E, Backinger CL, O’Connell ME, Vollinger RE Jr, Kaufman A, et al. Quit attempts and intention to quit cigarette smoking among young adults in the United States. Am J Public Health. 2007;97(8):1412–20. pmid:17600244
* View Article
* PubMed/NCBI
* Google Scholar
26. 26. Eum YH, Kim HJ, Bak S, Lee S-H, Kim J, Park SH, et al. Factors related to the success of smoking cessation: a retrospective cohort study in Korea. Tob Induc Dis. 2022;20:15. pmid:35221858
* View Article
* PubMed/NCBI
* Google Scholar
27. 27. Feng G, Jiang Y, Li Q, Yong H-H, Elton-Marshall T, Yang J, et al. Individual-level factors associated with intentions to quit smoking among adult smokers in six cities of China: findings from the ITC China Survey. Tob Control. 2010;19 Suppl 2(Suppl_2):i6-11. pmid:20935198
* View Article
* PubMed/NCBI
* Google Scholar
28. 28. Chen F-L, Chen PY, Tung T-H, Huang Y-C, Tsai M-C. The role of betel-quid chewing in smoking cessation among workers in Taiwan. BMC Public Health. 2014;14:755. pmid:25065303
* View Article
* PubMed/NCBI
* Google Scholar
29. 29. Yen AM-F, Chen S-C, Chang S-H, Chen TH-H. The effect of betel quid and cigarette on multistate progression of oral pre-malignancy. J Oral Pathol Med. 2008;37(7):417–22. pmid:18410311
* View Article
* PubMed/NCBI
* Google Scholar
30. 30. Yen AM-F, Chen S-C, Chen TH-H. Dose-response relationships of oral habits associated with the risk of oral pre-malignant lesions among men who chew betel quid. Oral Oncol. 2007;43(7):634–8. pmid:17466570
* View Article
* PubMed/NCBI
* Google Scholar
31. 31. Munpolsri P, Su CW, Chen SL, Yen AM. Behavior changes for smokers and betel quid chewers participating in the organized oral mucosal screening between 2010 and 2021 in Taiwan. Cancers. 2025;17.
* View Article
* Google Scholar
32. 32. Yang G, Ma J, Chen A, Zhang Y, Samet JM, Taylor CE, et al. Smoking cessation in China: findings from the 1996 national prevalence survey. Tob Control. 2001;10(2):170–4. pmid:11387539
* View Article
* PubMed/NCBI
* Google Scholar
33. 33. Anderson CM, Yip R, Henschke CI, Yankelevitz DF, Ostroff JS, Burns DM. Smoking cessation and relapse during a lung cancer screening program. Cancer Epidemiol Biomarkers Prev. 2009;18(12):3476–83. pmid:19959698
* View Article
* PubMed/NCBI
* Google Scholar
34. 34. Ashraf H, Tønnesen P, Holst Pedersen J, Dirksen A, Thorsen H, Døssing M. Effect of CT screening on smoking habits at 1-year follow-up in the Danish Lung Cancer Screening Trial (DLCST). Thorax. 2009;64(5):388–92. pmid:19052048
* View Article
* PubMed/NCBI
* Google Scholar
35. 35. Luh DL, Chen SLS, Yen AMF, Chiu SYH, Fann CY, Chen HH. Effectiveness of advice from physician and nurse on smoking cessation stage in Taiwanese male smokers attending a community-based integrated screening program. Tob Induc Dis. 2016;14:15.
* View Article
* Google Scholar
36. 36. Siewchaisakul P, Luh D-L, Chiu SYH, Yen AMF, Chen C-D, Chen H-H. Smoking cessation advice from healthcare professionals helps those in the contemplation and preparation stage: an application with transtheoretical model underpinning in a community-based program. Tob Induc Dis. 2020;18:57. pmid:32641923
* View Article
* PubMed/NCBI
* Google Scholar
37. 37. Tammemägi MC, Berg CD, Riley TL, Cunningham CR, Taylor KL. Impact of lung cancer screening results on smoking cessation. J Natl Cancer Inst. 2014;106(6):dju084. pmid:24872540
* View Article
* PubMed/NCBI
* Google Scholar
38. 38. Stead LF, Buitrago D, Preciado N, Sanchez G, Hartmann-Boyce J, Lancaster T. Physician advice for smoking cessation. Cochrane Database Syst Rev. 2013;2013(5):CD000165. pmid:23728631
* View Article
* PubMed/NCBI
* Google Scholar
39. 39. Rice VH, Hartmann-Boyce J, Stead LF. Nursing interventions for smoking cessation. Cochrane Database Syst Rev. 2013;(8):CD001188. pmid:23939719
* View Article
* PubMed/NCBI
* Google Scholar
40. 40. Carlebach S, Hamilton S. Understanding the nurse’s role in smoking cessation. Br J Nurs. 2009;18(11):672–4, 676. pmid:19525911
* View Article
* PubMed/NCBI
* Google Scholar
Citation: Munpolsri P, Su C-W, Yang H-F, Hsu T-H, Chou Y-Y, Lin L-J, et al. (2025) Changes in risk habits and influencing factors in the Taiwan oral cancer screening program. PLoS One 20(6): e0320461. https://doi.org/10.1371/journal.pone.0320461
About the Authors:
Pattaranan Munpolsri
Roles: Formal analysis, Software, Writing – original draft
Affiliation: School of Dentistry, College of Oral Medicine, Taipei Medical University, Taipei, Taiwan
Chiu-Wen Su
Roles: Data curation, Methodology
Affiliation: Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan
Hsu-Fei Yang
Contributed equally to this work with: Hsu-Fei Yang, Tsui-Hsia Hsu, Yen-Yu Chou, Li-Ju Lin, Chao-Chun Wu
Roles: Investigation, Project administration
Affiliation: Health Promotion Administration, Ministry of Health and Welfare, Taipei, Taiwan
Tsui-Hsia Hsu
Contributed equally to this work with: Hsu-Fei Yang, Tsui-Hsia Hsu, Yen-Yu Chou, Li-Ju Lin, Chao-Chun Wu
Roles: Investigation, Project administration
Affiliation: Health Promotion Administration, Ministry of Health and Welfare, Taipei, Taiwan
Yen-Yu Chou
Contributed equally to this work with: Hsu-Fei Yang, Tsui-Hsia Hsu, Yen-Yu Chou, Li-Ju Lin, Chao-Chun Wu
Roles: Funding acquisition, Project administration
Affiliation: Health Promotion Administration, Ministry of Health and Welfare, Taipei, Taiwan
Li-Ju Lin
Contributed equally to this work with: Hsu-Fei Yang, Tsui-Hsia Hsu, Yen-Yu Chou, Li-Ju Lin, Chao-Chun Wu
Roles: Funding acquisition, Project administration
Affiliation: Health Promotion Administration, Ministry of Health and Welfare, Taipei, Taiwan
Chao-Chun Wu
Contributed equally to this work with: Hsu-Fei Yang, Tsui-Hsia Hsu, Yen-Yu Chou, Li-Ju Lin, Chao-Chun Wu
Roles: Funding acquisition, Project administration
Affiliation: Health Promotion Administration, Ministry of Health and Welfare, Taipei, Taiwan
Sam Li-Sheng Chen
Roles: Methodology, Supervision
Affiliation: School of Oral Hygiene, College of Oral Medicine, Taipei Medical University, Taipei, Taiwan
ORICD: https://orcid.org/0000-0001-9750-3015
Amy Ming-Fang Yen
Roles: Conceptualization, Methodology, Supervision, Validation, Writing – review & editing
E-mail: [email protected]
Affiliation: School of Oral Hygiene, College of Oral Medicine, Taipei Medical University, Taipei, Taiwan
[/RAW_REF_TEXT]
[/RAW_REF_TEXT]
[/RAW_REF_TEXT]
1. Raghavi S, Anbarasu K. Unravelling the role of key genes in oral cancer progression: a comprehensive review. Oral Oncology Reports. 2024;10:100384.
2. Canadian Cancer Society. Risk factors for oral cancer. 2024. https://cancer.ca/en/cancer-information/cancer-types/oral/risks
3. Bagnardi V, Rota M, Botteri E, Tramacere I, Islami F, Fedirko V, et al. Alcohol consumption and site-specific cancer risk: a comprehensive dose-response meta-analysis. Br J Cancer. 2015;112(3):580–93. pmid:25422909
4. Gupta B, Johnson NW. Systematic review and meta-analysis of association of smokeless tobacco and of betel quid without tobacco with incidence of oral cancer in South Asia and the Pacific. PLoS One. 2014;9(11):e113385. pmid:25411778
5. Janbaz KH, Qadir MI, Basser HT, Bokhari TH, Ahmad B. Risk for oral cancer from smokeless tobacco. Contemp Oncol (Pozn). 2014;18(3):160–4. pmid:25520574
6. Anwar N, Pervez S, Chundriger Q, Awan S, Moatter T, Ali TS. Oral cancer: clinicopathological features and associated risk factors in a high risk population presenting to a major tertiary care center in Pakistan. PLoS One. 2020;15(8):e0236359. pmid:32760151
7. Jose M, Rajagopal V, Thankam FG. Chapter 9 - Oral tissue regeneration: Current status and future perspectives. In: Sharma CPBT-RO. Academic Press; 2021: 169–87. https://www.sciencedirect.com/science/article/pii/B9780128210857000099
8. Xiao X, Wang Z. Oral Cancer. Pharynx - Diagnosis and Treatment. IntechOpen; 2021. https://doi.org/10.5772/intechopen.97330
9. Chen Z, Chan ABW, Kam L-S, Chan M-H, Chan JYK, Lee W-T, et al. Changes in the incidence and human papillomavirus-Positive portion of oropharyngeal squamous cell carcinoma in Hong Kong. Cancers (Basel). 2024;16(1):226. pmid:38201653
10. Senevirathna K, Pradeep R, Jayasinghe YA, Jayawickrama SM, Illeperuma R, Warnakulasuriya S, et al. Carcinogenic effects of areca nut and its metabolites: a review of the experimental evidence. Clin Pract. 2023;13(2):326–46. pmid:36961055
11. Tapak L, Ghasemi MK, Afshar S, Mahjub H, Soltanian A, Khotanlou H. Identification of gene profiles related to the development of oral cancer using a deep learning technique. BMC Med Genomics. 2023;16(1):35. pmid:36849997
12. Poell JB, Wils LJ, Brink A, Dietrich R, Krieg C, Velleuer E, et al. Oral cancer prediction by noninvasive genetic screening. Int J Cancer. 2023;152(2):227–38. pmid:36069231
13. Lechner M, Liu J, Masterson L, Fenton TR. HPV-associated oropharyngeal cancer: epidemiology, molecular biology and clinical management. Nat Rev Clin Oncol. 2022;19(5):306–27. pmid:35105976
14. Pérez Jardón A, Arroyo E, Gándara Vila P, Pérez-Sayáns M. Risk factors of oral cancer: identification and mechanism of prevention. Handbook of Cancer and Immunology. Springer International Publishing; 2023: 1–29. https://doi.org/10.1007/978-3-030-80962-1_331-1
15. Aghiorghiesei O, Zanoaga O, Nutu A, Braicu C, Campian RS, Lucaciu O. The world of oral cancer and its risk factors viewed from the aspect of microRNA expression patterns. Genes. 2022;13.
16. Roman BR, Aragones A. Epidemiology and incidence of HPV-related cancers of the head and neck. J Surg Oncol. 2021;124(6):920–2. pmid:34558067
17. Sankaranarayanan R, Ramadas K, Thara S, Muwonge R, Thomas G, Anju G, et al. Long term effect of visual screening on oral cancer incidence and mortality in a randomized trial in Kerala, India. Oral Oncol. 2013;49(4):314–21. pmid:23265945
18. Rajaraman P, Anderson BO, Basu P, Belinson JL, Cruz AD, Dhillon PK, et al. Recommendations for screening and early detection of common cancers in India. Lancet Oncol. 2015;16(7):e352-61. pmid:26149887
19. Chuang S-L, Su WW-Y, Chen SL-S, Yen AM-F, Wang C-P, Fann JC-Y, et al. Population-based screening program for reducing oral cancer mortality in 2,334,299 Taiwanese cigarette smokers and/or betel quid chewers. Cancer. 2017;123(9):1597–609. pmid:28055109
20. Chuang S-L, Wang C-P, Chen M-K, Su WW-Y, Su C-W, Chen SL-S, et al. Malignant transformation to oral cancer by subtype of oral potentially malignant disorder: a prospective cohort study of Taiwanese nationwide oral cancer screening program. Oral Oncol. 2018;87:58–63. pmid:30527244
21. Ghani WMN, Razak IA, Yang Y-H, Talib NA, Ikeda N, Axell T, et al. Factors affecting commencement and cessation of betel quid chewing behaviour in Malaysian adults. BMC Public Health. 2011;11:82. pmid:21294919
22. Lai C-S, Shieh T-Y, Yang Y-HC, Chong M-Y, Hung H-C, Tsai C-C. Factors associated with quitting areca (betel) quid chewing. Community Dent Oral Epidemiol. 2006;34(6):467–74. pmid:17092276
23. Wang J-H, Yang Y-F, Zhao S-L, Liu H-T, Xiao L, Sun L, et al. Attitudes and influencing factors associated with smoking cessation: An online cross-sectional survey in China. Tob Induc Dis. 2023;21:87. pmid:37377525
24. Yeom H, Lim H-S, Min J, Lee S, Park Y-H. Factors affecting smoking cessation success of heavy smokers registered in the intensive care smoking cessation camp (Data from the National Tobacco Control Center). Osong Public Health Res Perspect. 2018;9(5):240–7. pmid:30402379
25. Fagan P, Augustson E, Backinger CL, O’Connell ME, Vollinger RE Jr, Kaufman A, et al. Quit attempts and intention to quit cigarette smoking among young adults in the United States. Am J Public Health. 2007;97(8):1412–20. pmid:17600244
26. Eum YH, Kim HJ, Bak S, Lee S-H, Kim J, Park SH, et al. Factors related to the success of smoking cessation: a retrospective cohort study in Korea. Tob Induc Dis. 2022;20:15. pmid:35221858
27. Feng G, Jiang Y, Li Q, Yong H-H, Elton-Marshall T, Yang J, et al. Individual-level factors associated with intentions to quit smoking among adult smokers in six cities of China: findings from the ITC China Survey. Tob Control. 2010;19 Suppl 2(Suppl_2):i6-11. pmid:20935198
28. Chen F-L, Chen PY, Tung T-H, Huang Y-C, Tsai M-C. The role of betel-quid chewing in smoking cessation among workers in Taiwan. BMC Public Health. 2014;14:755. pmid:25065303
29. Yen AM-F, Chen S-C, Chang S-H, Chen TH-H. The effect of betel quid and cigarette on multistate progression of oral pre-malignancy. J Oral Pathol Med. 2008;37(7):417–22. pmid:18410311
30. Yen AM-F, Chen S-C, Chen TH-H. Dose-response relationships of oral habits associated with the risk of oral pre-malignant lesions among men who chew betel quid. Oral Oncol. 2007;43(7):634–8. pmid:17466570
31. Munpolsri P, Su CW, Chen SL, Yen AM. Behavior changes for smokers and betel quid chewers participating in the organized oral mucosal screening between 2010 and 2021 in Taiwan. Cancers. 2025;17.
32. Yang G, Ma J, Chen A, Zhang Y, Samet JM, Taylor CE, et al. Smoking cessation in China: findings from the 1996 national prevalence survey. Tob Control. 2001;10(2):170–4. pmid:11387539
33. Anderson CM, Yip R, Henschke CI, Yankelevitz DF, Ostroff JS, Burns DM. Smoking cessation and relapse during a lung cancer screening program. Cancer Epidemiol Biomarkers Prev. 2009;18(12):3476–83. pmid:19959698
34. Ashraf H, Tønnesen P, Holst Pedersen J, Dirksen A, Thorsen H, Døssing M. Effect of CT screening on smoking habits at 1-year follow-up in the Danish Lung Cancer Screening Trial (DLCST). Thorax. 2009;64(5):388–92. pmid:19052048
35. Luh DL, Chen SLS, Yen AMF, Chiu SYH, Fann CY, Chen HH. Effectiveness of advice from physician and nurse on smoking cessation stage in Taiwanese male smokers attending a community-based integrated screening program. Tob Induc Dis. 2016;14:15.
36. Siewchaisakul P, Luh D-L, Chiu SYH, Yen AMF, Chen C-D, Chen H-H. Smoking cessation advice from healthcare professionals helps those in the contemplation and preparation stage: an application with transtheoretical model underpinning in a community-based program. Tob Induc Dis. 2020;18:57. pmid:32641923
37. Tammemägi MC, Berg CD, Riley TL, Cunningham CR, Taylor KL. Impact of lung cancer screening results on smoking cessation. J Natl Cancer Inst. 2014;106(6):dju084. pmid:24872540
38. Stead LF, Buitrago D, Preciado N, Sanchez G, Hartmann-Boyce J, Lancaster T. Physician advice for smoking cessation. Cochrane Database Syst Rev. 2013;2013(5):CD000165. pmid:23728631
39. Rice VH, Hartmann-Boyce J, Stead LF. Nursing interventions for smoking cessation. Cochrane Database Syst Rev. 2013;(8):CD001188. pmid:23939719
40. Carlebach S, Hamilton S. Understanding the nurse’s role in smoking cessation. Br J Nurs. 2009;18(11):672–4, 676. pmid:19525911
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
© 2025 Munpolsri et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Abstract
This study examines changes in oral risk habits and identifies factors influencing these changes among participants in a population-based oral cancer screening program to support effective public health interventions. The study included 2,569,920 individuals aged 30 and older who participated in Taiwan’s Oral Cancer Screening Program at least twice between 2010 and 2021. Changes in cigarette smoking and betel quid chewing were assessed between the first and last screenings and categorized as improved, unchanged, or worsened. A logistic regression model evaluated factors associated with habit improvement, including baseline oral habits, sex, age, education, screening adherence, and oral potentially malignant disorder (OPMD) findings. Among participants, 25.3% improved their oral habits. Baseline habits influenced how OPMD screening results affected behavior change. Among smokers, a positive screening result increased the likelihood of quitting or reducing smoking (adjusted odds ratio [aOR] = 1.18, 95% CI 1.16–1.20). However, among betel quid chewers, whether or not they smoked, a positive screening result was negatively associated with improved habits (aOR 0.79–0.88). Being female, older, college-educated, and regularly attending screenings were positively linked to behavior improvement. The program led to habit improvements in about one-quarter of participants, particularly older individuals, those with higher education, and frequent attendees. However, a diagnosis of OPMD motivated change only among smokers, not those engaging in both smoking and betel quid chewing, highlighting a lack of awareness in high-risk groups. Strengthening collaboration between health organizations and the screening program could enhance public awareness, improve program effectiveness, reduce oral cancer incidence, and lower long-term healthcare costs.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer