This was a cross-sectional descriptive-analytical study. Statistical population of the study consisted of male schoolteachers who aged more than 30 and were affiliated to the Department of Education of Qaenat County, Iran. Based on the findings of an earlier study into HL (
17), using the sample size calculation formula for the estimation of a proportion, and with a confidence interval of 95%, probability value of 0.29, and degree of freedom of 0.07, the sample size was calculated to be 162. However, in order to increase the study power, 202 schoolteachers were selected. Sampling was done through stratified random sampling so that all schools in Qaenat county were divided into four strata, namely junior elementary, senior elementary, junior high, and senior high schools. Then, the lists of all teachers in these schools were obtained from the Qaenat Department of Education. Then, a proportionate sample was selected from each stratum through simple random sampling. The inclusion criteria included consent for participation in the study, age of more than 30, and no university degree in medical sciences. Teachers were excluded if they incompletely answered study instruments.
3.1. Data Collection and Instruments
Data collection instruments were a demographic questionnaire, the short test of functional health literacy in adults, Sherer’s GSE scale, and Mularcik’s HSE scale. The demographic questionnaire included 15 items on teachers’ demographic characteristics such as age, educational level, marital status, number of children, smoking status, weight, height, diastolic and systolic blood pressures, and family history of hypertension.
The short test of functional health literacy in adults (S-TOFHLA) is the short version of TOFHLA and needs comparatively shorter amount of time (7 - 10 minutes) for answering. S-TOFHLA used in the present study contained 36 multiple-choice questions. Each question had only a correct answer, which was selected from four options and was scored 1. Wrong answers were scored 0. Thus, the total score of the test was 0 - 36 (
18). Teachers with S-TOFHLA scores of 0 - 16, 17 - 22, and 23 - 36 were considered to have inadequate, borderline, and adequate HL, respectively. The Persian S-TOFHLA is a valid and reliable test with a Cronbach’s alpha of 0.78 (
15).
Sherer’s GSE Scale included 17 items, which were scored on a five-point Likert-type scale from 1 “completely disagree” to 5 “completely agree”, with a total score of 17 - 85. The scores of this scale were interpreted as the following: 17 - 33, low GSE; 34 - 51, moderate GSE; and 52 - 85, high GSE. The Persian version of the scale was reported to have a Guttman split-half coefficient of 0.76 and a Cronbach’s alpha of 0.79 (
19).
Mularcik’s HSE scale (
20) included six items on factors contributing to hypertension, namely physical activity, cigarette smoking, stress, dietary regimen, daily activities, and medications. Items were scored on a ten-point Likert-type scale from 1 “completely disagree” to 10 “completely agree”, resulting in a total score of 6 - 60. Scores were interpreted as follows: 6 - 32, low HSE; 33 - 44, moderate HSE; and 45 - 60, high HSE. The content validity of this scale was assessed in the present study by 10 specialists. Its test-retest stability coefficient, total Cronbach’s alpha, and subscale Cronbach’s alpha values in the present study were 0.99, 0.96, and 0.79 - 0.94, respectively.
For data collection, study participants were asked to personally complete the study instruments. Moreover, their right-hand blood pressures were measured using a digital sphygmomanometer (Omron Healthcare, Japan) in the sitting position. Before blood pressure measurement, they were required to urinate completely, avoid drinking coffee, smoking cigarette, do vigorous physical activity for 30 minutes, and sit in the sitting position for at least five minutes. Participants with a diastolic blood pressure of 80 - 89 mmHg or a systolic blood pressure of 120 - 139 mmHg were considered as prehypertensive (
6). Height and weight were also measured based on the Center for Disease Control and Prevention standards and using a portable height scale and a digital weight scale (both made in Australia). Then, body mass index (BMI) was calculated. Participants with BMIs of 18.5 - 24.9, 25 - 29.9, and more than 30 were considered as normal, overweight, and obese, respectively (
6).
Data were entered into the SPSS program (V. 19.0). The Kolmogorov-Smirnov test indicated that all study variables had normal distribution. Therefore, the independent-sample t, Chi-square, Tukey’s post hoc tests, Pearson correlation analysis, and one-way analysis of variance were employed for data analysis at a significance level of less than 0.05.
This study was approved by the Institutional Review Board and the Ethics Committee of Mashhad University of Medical Sciences, Mashhad, Iran (with the approval codes of 950139 and IR.MUMS.REC.1395.597, respectively). Participants were provided with explanations about the study aim and then, were asked to provide consent for participation.