First, an ethical code (IR.IAU.TMU.REC.1397.163) and approval of the Ethics Committee of the University were acquired. Then, a letter of introduction was received from the Research Department of the Islamic Azad University of Tehran Medical Sciences. Finally, after obtaining the agreement of the Research Department of Lorestan University of Medical Sciences, the authors referred to Imam Khomeini Hospital in Pol-e Dokhtar. A total of 56 patients with ischemic heart disease were chosen through simple random sampling according to the table introduced by Krejcie and Morgan. Rand list software was used to classify patients into the experimental and control groups.
The inclusion criteria were the lack of formal training in empowerment programs, lack of perceptual problems (e.g., attention deficit disorder) according to the patient’s profile, no history of mental illness (depression, neuroticism, violence, obsessive-compulsive disorder, etc.) according to the patient’s profile, lack of employment in healthcare areas, and lack of prior hospitalization for treating and controlling ischemic heart disease. Alternatively, the exclusion criteria were the lack of phone call access to the patient and his/her family during the research process, the occurrence of a stressful event for the patient during the intervention (stress, pain, depression, etc.), and patient’s death due to the illness. The data collection tool consisted of, first, a questionnaire covering the patients’ demographic and clinical information and, second, the career decision self-efficacy scale (CDSES) designed and validated by Lorig (1996).
CDSES contains 33 questions to examine patients’ self-efficacy in 10 areas. The first three questions address regular exercise, question 4 is related to disease information, questions 5 to 8 deal with assistance by the community, family, and friends, questions 9 to 11 are related to the relationship with the physician, questions 12 to 16 cover disease management, questions 17 to 19 cover habitual activities, questions 20 and 21 cover social and recreational activities, questions 22 to 26 cover symptom management, question 27 is related to managing shortness of breath, and the last six questions address depression management. Each item is scored on a 10-point Likert scale. If the score of the questionnaire is between 1 and 33, the degree of the variable is low; if it is between 33 and 165, the degree of the variable is moderate; and if it is above 165, the degree of the variable is very high. Hatef et al. (
21) obtained the content validity of this scale and established its validity (0.93) based on Cronbach’s alpha. The reliability of the questionnaire was 0.84 based on Cronbach’s alpha.
In the first session, the goals of the study were described and informed consent forms were obtained from the patients. Then, both questionnaires were completed by the researcher for experimental and control groups. Some of the educational materials were presented to the patients in this session. In the following days, based on the suggested time, two other educational sessions were held for patients in the experimental group. After the end of the training sessions, the post-test was performed in both groups. Then, four weeks (first phase of control) and eight weeks (second phase of control) post-intervention when the patients had been discharged, both groups were called to the heart clinic to complete CDSES. In cases where patients did not return for the follow-up, the researcher referred to their house.
The content of the intervention was presented according to the program’s instructions from the second day of hospitalization. The training sessions were held between 11 and 12 A.M. so as not to interfere with visiting hours or physician rounds of the ward. All the three sessions (each lasting 45 minutes) were organized by the researcher in groups of three to five people in the patient room over six weeks on Mondays, Tuesdays, and Wednesdays. Participants were separated based on gender before attending the sessions.
The aim of the empowerment intervention in this study was to provide an integrated training program in the form of a booklet. The educational content in the booklet encompassed the recognition of the nature of the disease, different causative and predisposing factors of ischemia and myocardial infarction, signs and symptoms of the disease, exacerbating and relieving factors, diagnostic procedures, warning and discernable symptoms, general and medical treatment methods, disease control agents, medications (including nitrates, antihyperlipidemic agents, beta blockers, calcium blockers, and antiplatelet drugs), diet, relevance of weight control and obesity prevention, exercise benefits, avoiding substance abuse, stress control, specific self-care instructions, allowable and restricted activities, and different measures for stress reduction.
In the second session, the topics taught in the previous session were reviewed and patients’ questions were answered. Moreover, a new subject was discussed. Similarly, the third sessions focused on teaching and responding to patients’ questions about the instructions provided in the previous sessions and the booklet. In the end, the materials were recapitulated and more significant topics were highlighted. It must be added that after the second control stage and data collection, the control group was also exposed to the empowerment training program for three sessions as the experimental group.
SPSS version 23 was used to analyze the obtained data. At the level of descriptive statistics, measures such as mean and standard deviation, skewness, and kurtosis were used to analyze descriptive indices. Moreover, the Kolmogorov-Smirnov test was used to check the normality of data. As for inferential statistics, covariance analysis and independent t test were used to compare the means of experimental and control groups.