This clinical trial was conducted after obtaining permission from the Ethics Committee of Zabol University of Medical Sciences (code: IR.ZBMU.REC.1397.204). The study sample included 60 patients undergoing angiography in the coronary care unit (CCU) of Ali-Ibn Abi-Taleb Hospital in Zahedan, located in southeast of Iran. Sixty patients who met the inclusion criteria were randomly selected and assigned to three groups (20 subjects per group), including two intervention groups and a control group. The inclusion criteria were as follows: having a physician order for coronary angiography at least one day before the procedure; being in the age range of 30 to 60 years; having the ability to speak and understand Persian; having minimum literacy; having no visual or hearing impairment; no history of angiography; not using sleeping pills, sedatives, or strong analgesics; having no severe pain due to the nature of the disease, and having no history of known psychological problems or anxiety disorders. On the other hand, the exclusion criteria were leaving the study, having an emergency angiography order, and patient’s death at any stage of the study.
The instruments used to collect the data included a demographic information form and the Depression, Anxiety, and Stress scale (DASS-21). The demographic information form documented the participant’s age, gender, occupation, years of education, and marital status. Moreover, the stress and anxiety subscales of DASS-21 were used in this study. Each subscale contained seven items, scored on a four-point Likert scale (from “very untrue of me” = 0 to “very true of me” = 3). A higher score on this scale indicates higher levels of anxiety and stress in the patient. The reliability of the anxiety and stress subscales was estimated at 0.81 and 0.89, respectively, based on Cronbach’s alpha method (
15). The corresponding values reported by Brown et al. (
16) were 0.89 and 0.93, respectively, and the values reported by Siamak Samani (
17) were 0.75 and 0.87, respectively. In the present study, Cronbach’s alpha coefficients for the two subscales of anxiety and stress were 0.79 and 0.92, respectively.
The patients who met the inclusion criteria were selected using convenience sampling. The participants were randomly assigned to the nursing consultation, guided imagery, and control groups after providing their written consent. The DASS-21 was completed on the first day of hospitalization and before the intervention for each patient. The participants in the nursing consultation group received face-to-face training individually and orally on the day before angiography. The training program content included instructions about the anatomy and physiology of blood and heart circulation, pathophysiology of CAD, risk factors, elective treatments (including angiography), possible risks and complications of angiography, length of hospital stay, and expected results. The maximum duration of training was two hours, depending on the needs of the hospitalized patient.
The guided imagery audio file (including relaxing music, visualization of beautiful seaside landscapes with a positive accent for increasing mental health, and repetition of relaxing words, such as God, love, beauty, and cheerfulness), prepared by the researcher, was played using headphones for each participant in the guided imagery group 20 minutes before angiography. To control for intervening factors, such as noise in the ward, the intervention was performed in a quiet environment in the researcher’s presence. Before angiography, DASS-21 was completed by the participants in the three groups as the post-test.
The collected data were analyzed in SPSS version 25 using statistical tests, such as analysis of variance (ANOVA), Tukey’s post-hoc test, analysis of covariance (ANCOVA), paired samples t-test, Fisher’s exact test, and chi-square test at a significance level of 0.05 (P < 0.05).