This trial was a prospective, non-randomized, controlled study (a quasi-experimental study), which was conducted in April 2013. Each patient was randomly assigned to one of the three groups: control, traditional (face-to-face), and SMS. This study was conducted after asking permission and a letter of introduction from the deputy research of Ahvaz Jundishapour University of Medical Sciences, department of nursing and midwifery (ETH Code-536) and the chairmen of Abadan city’s hospitals and referring to the emergency of Abadan city’s hospitals (Iran) and by sampling method of convenience.
In the study by Park et al. (
33) the sample size was estimated at 17 people in each group, with a test power of 90%. In this current study, sampling was conducted after presenting the participants with the necessary information about the research aim and asking them for written testimonials for participating in the study. They were reassured that their registered personal information would not be revealed. They were also advised that the study was based on the formula of a sample volume, and what the criteria were for entering the study. Each group consisted of 25 participants who met the following criteria: being over 18 years old; suffering from hypertension, which was confirmed by a specialized physician; having the ability to answer questions and participate in educational sessions; starting at least 6 months’ treatment for controlling blood pressure (
30,
34); controlling their blood pressure by at least one pill; were not suffering from any specific and weakening disease; average or weak following toward treatment; having a cell phone; and having the ability to read SMS. The criteria for exiting the study included: suffering from any kind of disease that interfered with the process of research, such as chronic kidney failure, brain, a heart attack; any medicinal dependency except for hypertension treatment; non-participation in two sessions of education; no sending without text short message to the server within 2 days.
To prevent any bias in the study results and to ensure that the study participants did not get in touch with each other and transfer information between themselves (two groups of interference and one group of control), each group was selected randomly (by drawing lots) from three hospitals in Abadan city. The sampling was conducted by the researcher among the patients suffering from hypertension using the convenience sampling method and regarding characteristics of under-research units and criterion for entering in study.
In this study, each of the three groups were similar to each other in terms of age, gender, level of education, marital status, and duration of suffering from hypertension. Questionnaires were filled out by the researcher in the form of interviews and those patients whose answer points were average or low regarding following the treatment (points between 22 and 65) could enter the study. Their blood pressure was taken by observing the measurement indexes. During the research, the blood pressure apparatus was calibrated daily. After finishing these steps, the necessary explanation about the method of teaching was presented to the participants.
After coordinating with the participants in the face-to-face education group who entered in study from the Taleghani hospital of Abadan, the sessions were regulated as eight educational sessions of 30 minutes each, twice a week in two groups of eight participants and one group of nine participants. The same educational content that was presented in the face-to-face group was sent in the form of SMS for the distance education group who entered the study from the Shahid Beheshti hospital. Within 4 weeks, the control group received two fluent and attractive sentences in the form of an SMS between 8 a.m. and 8 p.m. daily for preventing from mental disturbance , every second message had the same subject and researchers tried to come to a conclusion about every discussed subject rapidly, on the same day, or ultimately within 3 days. Every day, the first message was sent in the form of semi-predicative and semi-interrogative text in order for people to prepare mentally; therefore, the first question was answered in the following message and this made the participants prepare for the next message. To make sure they received and read the messages, researchers asked the participants to send back an empty message after receiving two daily messages. They were also asked to send in any cell phone costs. Participants of the control group were selected among the eligible patients referred to 17 Shahrivar hospital of Abadan.
After finishing the education program, all three groups were given 2 months to implement the learned information into their daily lives (
24,
35). Participants of both interference groups were contacted once a week on a day they were informed about it and researchers answered their probable questions; moreover, the participants were provided with a phone number so they could give the researcher a call anytime there was a problem. After mentioned time, questionnaires were filled in again for the three groups by the researcher at the same place. It is noticeable that during this study, three participants of the face-to-face interference group exited from the study because they did not participate in more than two educational sessions.
In this study, the tool of collecting data consisted of three questionnaires. The demographic information registration questionnaire consisted of 15 questions and was provided in two parts. The personal information part examined age, gender, nationality, marital status, and level of education. The disease history part examined the duration of suffering from hypertension, the number of pills taken, and the type of medicine taken. The second questionnaire related to following the medicinal diet and the medicinal diet questionnaire (N = MMAS-8) applied (MMAS-4 is the most recent version of it). This questionnaire consisted of eight questions, and yes/no answers were regulated for seven of them. The score for a “yes” answer was 1, and for a “no” answer was 0. In the final question, answers were regulated as a 5-point Likert scale, which gives a score of 0 to answers of “never” or “rarely” and a score of 1 to other answers. A final point of 0 - 2, and points over 2, were considered as following medicine and not following, respectively (
36).
Second part of questionnaire is related to following the remedial diet. It was regulated in the form of 22 questions and was based on presented recommendations for therapeutic lifestyle changes and a dietary approach to stop hypertension. Question numbers 1 - 5 examined the mount of following recommended diet by patient. Answers were regulated as the 5-point Likert scale, and the options were scored as 1 - 5 in accordance with the accuracy of each patient’s function. Points were estimated as weak, average, good, and excellent by obtaining 15 - 30, 31 - 45, 46 - 60, and 61 -75 points, respectively. Question number 16 was allocated to the patient’s physical activity and was scored by a 5-point Likert scale. Patients were considered as weak, average, good, and excellent by obtaining scores of 1, 2, 3, 4, and 5, respectively. Questions 17 - 22 examined the amount of lifestyle modifications required, such as stopping smoking, stopping or reducing alcohol intake, controlling stress, losing weight, and taking painkillers. Questions 17 - 21 were scored by a 5-point Likert scale. In question number 22, each patient’s body mass index (BMI) of 10 was in the normal range of 18 - 25 and obtained 5 scores and a BMI over normal obtained 1 score. Ultimately, patients estimated as weak, average, good, and excellent obtained scores of 6 - 11, 12 - 17, 18 - 23, and 24 - 30, respectively.
The third questionnaire was related to testing the patients’ awareness of their disease and consisted of 27 questions of three options: “yes”, “wrong” and “I do not know” answers; scores of 2, 0, and 1 were allocated to each answer, respectively. Ultimately, obtaining scores of 0 - 17, 18 - 35, and 36 - 54 were considered as weak, average, and good, respectively.
After translating the main form of the questionnaire of following the medicinal diet by two experts of the English language, its Persian translation was delivered to three other English experts to translate it to the source language to ensure its accuracy. Then, the questionnaires (demographic, evaluation of awareness, following medicinal diet) were delivered to 10 members of the Ahvaz nursing and midwifery faculty. A final version was then regulated after any necessary modifications and was given to 10 participants to determine the stability of this type of data-collecting tool. After its collection, the interior correlation of data was examined by Cronbach’s alpha coefficient that 85% coefficient indicating reliability of tool. In order to confirm the stability of the blood pressure measurement apparatus, other mercurial pressure gauge for arms with the Alpeka 2 brand applied and two blood pressure measured by any apparatus compared with each other daily and in order to estimate the stability of weight, a 1 kg weight control used daily. In this study, SPSS software Version 20 and analysis tests of one way variance applied for analysis of datum, the Toki test and the Chi-square test for two-by-two comparisons, and the paired T-test for the comparison of quantity variables before and after interference were used.