This was a quasi-experimental study conducted among 32 senior undergraduate midwifery students from December to February 2018. Sampling was performed using the census method, and all the senior midwifery students were enrolled. The students had completed all the clinical and theoretical units in obstetrics and gynecology areas and were willing to participate in the study. Guest students, students with previous clinical experience, working in midwifery or clinical centers, and those who had previously received training on prescription were excluded from the study. The study was approved by the Ethics Committee of Babol University of Medical Sciences (IR.MUBABOL.REC.1398.016).
The data collection tools included a demographic information form (including marital status, age, residential location, and grade point average) and OSCE test and checklist scoring. The OSCE test included four stations in four common domains in gynecology including treatment of trichomoniasis vaginitis, cervicitis, pelvic inflammatory disease, and abnormal uterine bleeding. The duration of the OSCE was 20 minutes. First, the students took a history from a simulated patient, and then they prescribed a prescription within 5 minutes to fit each case of the disease. The answer to each question was entered in a separate rating form. Adherence to the principles of prescribing by the students was evaluated using a checklist before and after training and four weeks later. The checklist was prepared based on the principles of rational treatment of the WHO (
11,
12), the National Committee on Rational Drug Administration and Consumption, and the Department of Food and Drug of Iran's health ministry (
13).
The validity and internal consistency of the OSCE tests were assess using face and content validity and Cronbach's alpha coefficient, respectively. A qualitative method was used to assess face validity, and quantitative and qualitative methods were used to assess content validity. To assess the face validity, experts and 10 students were separately asked to comment on difficulty level, inadequacy, phrase ambiguity and deficiencies in the meanings of the words, and then the necessary changes were made to the questionnaire. For the purpose of qualitative content validity, experts were asked to provide feedback on grammar, the use of appropriate words and the importance of questions. After collecting expert opinions, the necessary changes to the tool were considered. For the quantitative assessment of content validity, content validity ratio (CVR), and content validity index (CVI) were measured. To calculate the CVR, the questionnaire was sent to 11 specialists in midwifery and medical education and were asked to answer each of the tool questions as “necessary”, “not necessary but useful” and “not necessary”. Responses were calculated based on the formula. The numbers above 0.59 were accepted. To calculate the CVI, the questionnaire was given to the previous experts and their opinions were collected for each question on the relevance, clarity, and simplicity based on a 4-point Likert scale from 0 to 3 (such as irrelevant, somewhat relevant, relevant, completely relevant). CVI score was higher than 0.79. To establish the reliability, a pilot study was carried out and the questionnaire was completed by 30 university students other than the actual study participants. Two weeks later, they were asked to complete the questionnaires again. The standardized Cronbach’s alpha reliability coefficient was 0.82. After confirmation of the initial reliability, the study was conducted.
The checklist was prepared in four parts including superscription (patient profile, name, age, phone number and address), general principles of prescription (header symbol, date, cause of visit, diagnosis, readability of the prescription, number of prescription drugs, name and signature of the writer of the prescription), standard principles of prescription (using the generic name of the drug, writing the full name of the drug, right spelling of drug name, correct drug, form of the drug, dose, and number of medications), and instructions for using the medication (how to use, drug use intervals, route of administration, use of abbreviated symbols or use of the phrase "as ordered or as needed", and drug side effects training). Each correct answer had one point and lack of an answer or an incorrect answer was given zero point. In this way, four scores were considered for the superscription, seven scores for general principles of prescription, eight scores for standard principles of prescription, and six scores for instructions for using the medication. The total score was 25. Since each participant provided four prescriptions in the four common domains of gynecology, 128 prescriptions were obtained from 32 participants.
To conduct the educational program, the students were divided into two equal groups. For each group, a two-day workshop was held, with each session taking 5 hours a day. Each group was divided into three subgroups for practical work. First, the researcher provided a description of the prescription and its importance. Then, the stages of rational treatment, personalized medicines, general principles of prescribing and how to write a prescription, drug forms, monitoring treatment and medication errors were described. The contents were organized using lectures and slideshows, whiteboard, question and answer, and review of the samples of existing medications. The educational content was derived from the principles of rational treatment of the WHO, the National Committee on Rational Drug Administration and Consumption, and the Department of Food and Drug of Ministry of Health (
11-
13). The educational program was then continued in the subgroups with practical training on 15 cases from prescription guideline (
13) and eight questions about gynecological diseases developed as a description of the disease by the researcher.
The data were analyzed using SPSS version 23. The normality of the variables was assessed by the Kolmogorov-Smirnov test. For descriptive statistics, frequency, percentage, mean ± standard deviation and percentage change were used. The percentage change was calculated for each of the four parts of the prescription principles (i.e., superscription, general principles of prescription, standard principles of prescription and instructions of using the medication) by the formula ([E - B] / B) × 100, where E is the end of intervention value and B is the baseline value.
In the repetitive measure analysis, the sphericity assumption must first be examined. The implication of the sphericity assumption is that the variance of the difference in observations in the study stages is the same. This assumption is tested in SPSS software with Mouchly test. Due to the P value of this test, which was less than 0.05, the sphericity assumption is not established. In other words, the variance of the differences between the different stages is not equal. Therefore, the Greenhouse-Geisser test was used in this study.
In all the tests, the confidence coefficient was 95%, and the significance level was 0.05.