The ethics committee of Zahedan University of Medical Sciences (IR.ZAUMS.REC.1400.050) approved the study protocol. Also, informed consent was obtained from all patients prior to the study.
This quasi-experimental study included 100 CAD patients hospitalized in the CCUs and post-CCUs. Using simple randomization method, the patients were assigned into two groups of intervention and control. Following a similar study Faraji et al. (
25), the sample size was estimated as 46 persons per group using the following formula with a 95% confidence level and 85% statistical test power. Considering the possibility of the participants’ dropout, the sample size for each group was considered as 50 persons (100 persons in total):
Z (1-α/2) = 1.96 (at a 95% confidence interval); Z (1-β) = 1.03 (with an 85% test power); S1 = 1, S2 = 7.75, = 9.78, and = 12.76.
The inclusion criteria were a definite diagnosis of CAD without myocardial infarction, aged 18 - 70 years, ejection fraction of higher than 40% (EF > 40%), the ability to speak and understand Persian, having minimum literacy, ability to communicate, non-attendance in similar face-to-face training programs, and the absence of mental disorders and severe chronic diseases (thyroid, cancer, obstructive lung disease, asthma and liver, and kidney damage). The exclusion criteria were the occurrence of any emergency for the patient, unwillingness to continue participation in the study, impossibility of communicating by phone, the patient’s failure to attend the training sessions, early discharge, non-participation in more than one training session, and the death of the patient.
The data in this study were collected using a demographic information form (age, gender, marital status, employment, education, place of residence, economic status, living conditions, and the disease-related variables, including the duration of the disease, underlying disease, and hospitalization history), the Brief Illness Perception Questionnaire (Brief IPQ), and the Cardiovascular Management Self-efficacy Scale (CMSES).
The Brief IPQ is a 9-item tool developed by Weinman et al. (1996) cited in Broadbent et al. to assess illness perception. The eight items (one open question is not included in the scoring) are ranked using a scale of 0 to 10. Items 3, 4, and 7 are reverse scored. A respondent’s total score ranges from 0 to 80. The Cronbach’s alpha value for the questionnaire was reported to be 0.80 and its test-retest reliability coefficient was reported from 0.42 to 0.75 (
26). In the present study, the reliability of the tool was calculated as 0.75 using Cronbach’s alpha coefficient.
The CMSES was developed by Steca et al. (2015) cited in Jafari Sejzi et al. in Italy. The scale contains nine items that assess a person’s confidence in their self-efficacy in disease management using a 5-point Likert scale, ranging from 0 (not at all confident) to 4 (completely confident). Higher scores show a better cardiovascular management self-efficacy. The scale has three dimensions: self-efficacy in cardiac risk factors, which consists of four items that assess patients' beliefs about their ability to faithfully follow a set of restrictions for smoking, diet, physical activity, and avoiding stressful situations; self-efficacy in following treatment, which consists of strong beliefs from two items showing patients' beliefs about their ability to remember to take medication correctly; and self-efficacy in diagnosing symptoms that evaluates patients' beliefs about the ability to recognize signs and symptoms of worsening disease. The total score ranges from 9 to 45. The reliability and validity of the Persian version of the scale were confirmed for use in the Iranian community, and its validity and reliability were assessed, and its psychometric properties were confirmed (80%) using Cronbach’s alpha coefficient (
27). The reliability of the instrument was assessed in this study, and its Cronbach’s alpha was reported to be 0.81.
After obtaining the ethical code, the researcher went to the heart departments of Zahedan teaching hospitals, presented the objectives of the study, and completed the three questionnaires (demographic, Brief IPQ, and the CMSES) for each patient by interviewing method. The teach-back method was carried out individually in three sessions over three days for the patients in the intervention group (
Table 1). The first training session was conducted at the patient’s bedside one day after hospitalization upon the stability of the patient’s condition. Each training session lasted for 30-45 minutes based on the patient’s tolerance and learning rate. A total of six patients were discharged before the completion of the intervention sessions. Thus, the third training session was held at the patient’s home upon prior arrangements. During the training session, the patient was asked to repeat the instructed concept or topic in their own words. If the patient did not understand the instructed material, the material was instructed again to them. Then, at the end of the third training session, an education pamphlet prepared based on the content of the training sessions was given to the patients in the intervention group. The patients in the control group received only routine training in the CCUs. On the day of discharge, the patients of this group were also given the same educational booklet as the intervention group. One month after the intervention, the patients in both groups were asked to attend the hospital and complete the questionnaires.
| Session | Focus | Content | Duration (min) |
|---|
| 1 | Illness perception | Getting familiar with the patient; establishing rapport with the patients and creating a reassuring environment; explaining the training sessions; making arrangements for subsequent sessions; defining the disease, its nature, symptoms, risk factors, duration of the disease, the disease outcomes, effective treatments and controlling measures; changing the patient’s misconceptions about the disease; asking the patient to reproduce the instructed materials; and resolving any problem faced by the patient. | 30 - 45 |
| 2 | Self-efficacy | Reviewing the instructed materials; discussing the patient’s diet and medication; the significance of not smoking; stress control; sexual health; asking the patient to reproduce the instructed materials; and resolving any problem faced by the patient. | 30 - 45 |
| 3 | Overview | Reviewing the instructed materials; highlighting important issues; asking the patient’s opinions about the impact of the instructed materials; giving an educational pamphlet to the patient; asking the patient to reproduce the instructed materials; and resolving any problem faced by the patient. | 30 - 45 |
The Shapiro-Wilk test was used to assess the normal distribution of the data. The collected data were analyzed in the statistical package for the social sciences (SPSS v.22) software using the independent samples t-test, paired samples t-test, chi-square test, Fisher’s exact test, regression test, and analysis of covariance (ANCOVA) at a significant level of P < 0.05.
To improve the quality of implementing the feedback-based teaching method, special attention was paid to points such as the quality of the patients' memory, the patient's understanding of the various issues of the disease and its treatment, and the discovery of the patient's personality in terms of shyness. In the first training session, during the introduction, we assessed the quality of the patient's memory. Understanding the concepts related to the disease through open dialogue was considered in the interviews. By creating intimate and informal interviews, efforts were made to effectively reduce the patient's embarrassment in accepting the training and retelling these trainings without fear of the researcher. Also, at the end of each training session, the important and basic content was repeated, and the possible problems of the patients were resolved. This was emphasized with the principles of the feedback-oriented teaching method.