3.2. Participants, Sampling, and Intervention
According to
Figure 1, based on the initial screening process and the predefined inclusion and exclusion criteria, 178 students were deemed eligible to participate in the study. The sample size was calculated using the formula for comparing the means of two independent groups, with particular emphasis on the primary study outcomes, namely health literacy and self-efficacy. The calculation was based on the study conducted by Panahi et al. (
30), entitled "Effect of Health Belief Model-Based Education on Health Literacy and Smoking Prevention Among Students." Based on the reported means and standard deviations for health literacy (M = 72.51, SD = 5.64 in the intervention group and M = 62.21, SD = 5.54 in the control group) and self-efficacy (M = 28.24, SD = 3.24 in the intervention group and M = 26.89, SD = 3.54 in the control group), and a significance level of 0.05 (α = 0.05), the minimum required sample size was estimated to be 27 participants per group. To account for a potential attrition rate of 10%, the final sample size was increased to 30 participants per group, resulting in a total sample of 60 participants. During the screening phase, standardized questionnaires assessing health literacy, self-efficacy, and intention to smoke were administered to all eligible students. Individuals whose health literacy and self-efficacy scores were below the predefined cutoff values and whose intention-to-smoke scores exceeded the cutoff value were identified as at risk and, after meeting the inclusion and exclusion criteria, were enrolled in the study. After written informed consent was obtained, participants were randomly assigned to either the intervention group (n = 30) or the control group (n = 30) using a simple coin-toss randomization procedure, which provided an equal probability (50%) of allocation to either group. Participants were assigned to the intervention group if the outcome was heads and to the control group if the outcome was tails. To minimize selection bias, the randomization process was conducted by an individual independent of the research and intervention teams. The inclusion criteria were completion of at least two academic semesters and having smoked at least once during the previous week. The exclusion criteria included complete smoking cessation for at least two months before the study, use of substances other than cigarettes during the previous two months, participation in other smoking cessation programs or methods, and absence from more than two intervention sessions. After enrollment, baseline assessments (pre-test) were conducted. Subsequently, the intervention group participated in eight 90-minute educational sessions based on the health belief model and designed according to the World Health Organization protocol (
Table 1). During the intervention period, the control group received no specific educational program. A post-test assessment was conducted one week after completion of the intervention.
| Weeks | Session Durations | Provided Contents |
|---|
| First | 1.5 hours | Conducting a pre-test and learning about the dangers of nicotine |
| Second | 1.5 hours | Preparing a list of risks and dangers of smoking and the necessity of quitting smoking |
| Third | 1.5 hours | Investigating the extent and severity of students' concerns about the listed dangers |
| Fourth | 1.5 hours | Exploring disease prevention and the possible benefits of quitting smoking |
| Fifth | 1.5 hours | Examining the triggers of temptation, obstacles to smoking cessation, and disrupting factors in starting a smoking cessation program |
| Sixth | 1.5 hours | Exploring resources that can help reduce smoking, such as treatment centers, counseling centers, and self-help books |
| Seventh | 1.5 hours | Creating a timetable for reducing smoking over a six-month period |
| Eighth | 1.5 hours | Conducting post-tests, evaluating the success of the program, and conducting student interviews and surveys |
Random allocation sampling process
3.3. Measures
One of the tools used in this study was the attitudes toward smoking questionnaire, which was developed and validated by Riahi et al. in 2009 (
21). This questionnaire measures three variables: contact with smokers, a smoke-free and healthy environment, and participants' views on smoking-related laws. It consists of 32 closed-ended items scored on a five-point Likert scale, with scores ranging from 1 (strongly disagree) to 5 (strongly agree).
Questions 4, 5, 12, 13, 14, 15, 16, and 17 are scored in reverse order. A score between 32 and 54 indicates a negative attitude toward smoking, a score between 55 and 108 indicates a moderate attitude toward smoking, and a score above 109 indicates a positive attitude toward smoking. This questionnaire assesses three dimensions: cognitive, emotional, and behavioral. The reliability coefficient for the total questionnaire was 0.871. The reliability coefficients for the cognitive dimension (9 items), emotional dimension (11 items), and behavioral dimension (12 items) were 0.739, 0.825, and 0.876, respectively. The content validity ratio (CVR) was 0.62, and the content validity index (CVI) was 0.84.
To ascertain questionnaire validity, face validity was assessed to ensure the representativeness of the item content and the overall structure of the questionnaire through direct consultation with experts and specialists in the field, in addition to the use of scales developed in previous studies (
21).
To measure self-efficacy, the 17-item Sherer and Maddox questionnaire, standardized by Barati, was used (
22). The reliability of the questionnaire based on Cronbach's alpha was 0.79. Regarding questionnaire validity, there is a moderate negative correlation between the scores of the self-efficacy scale and the internal-external control scale developed by Sherer and Maddox. The CVR was 0.78, and the CVI was 0.79.
This scale comprises three components: the inclination to initiate behavior, the tendency to continue persisting and exerting effort, and the ability to maintain persistence in the face of failure. Scoring was based on a Likert scale from completely disagree (
1) to completely agree (
5). Questions 1, 3, 8, 9, 13, and 15 are scored in reverse order. Scores between 17 and 34 indicate weak self-efficacy, scores between 34 and 51 indicate moderate self-efficacy, and scores above 51 indicate very high self-efficacy (
23).
To measure health literacy, the 33-item scale developed by Tavoussi et al. in 2014 was used (
24). It measures individuals' abilities across various dimensions of health literacy, including reading skills (4 questions), access (6 questions), comprehension (7 questions), evaluation (4 questions), and decision-making and application of health information (12 questions) (
25).
This questionnaire uses a 5-point Likert scale. For questions related to reading skills, a score of 5 is assigned to "completely easy," 4 to "easy," 3 to "neither easy nor difficult," 2 to "difficult," and 1 to "completely difficult." For the other four dimensions of health literacy, a score of 5 is assigned to "always," 4 to "most of the time," 3 to "sometimes," 2 to "rarely," and 1 to "not at all" (
26).
Scoring was performed as follows: first, the raw score for each individual across the domains was obtained as the algebraic sum of the item scores. Subsequently, to convert this score to a range of zero to 100, the formula of the difference between the raw score and the minimum possible raw score divided by the difference between the maximum possible score and the minimum possible score was used. Finally, to calculate the total score, the scores of all dimensions, based on the established range of zero to 100, were summed and divided by the total number of dimensions.
Scores ranging from 0 to 50 are classified as insufficient health literacy, scores up to 66 reflect a not very sufficient level of health literacy, scores between 66 and 84 indicate sufficient health literacy, and scores from 84 to 100 are categorized as excellent health literacy. Moreover, this questionnaire has good validity and acceptable reliability. The CVR was 0.75, and the CVI was 0.81 (
27).