Study design and participants
This study is a cross-sectional study conducted during March 24 and April 7, 2020 in Shiraz; the fifth populous city located in Southwest of Iran. The study protocol was written based on the Helsinki ethical principles for medical researches and approved by the Ethics Committee affiliated to Shiraz University of Medical Sciences (SUMS) (IR.SUMS.REC.1398.1424).
The participants were pregnant mothers registered in maternity clinics affiliated to SUMS. The secretary of each maternity clinic contacted mothers through a phone call and introduce them the study and its goal. After reminding the participants their rights, they were asked to fill an online questionnaire. Pregnant mothers included in this study if they were visited by an obstetrician working in maternity clinics affiliated to SUMS. On the other hand, pregnant mothers were excluded from the study if
- They did not answer their phone for three times.
- They were reluctant to participate.
- They had not been living in Shiraz for at least 6 months prior to the study.
Finally, 540 pregnant mothers sent us a completed questionnaire. (Figure 1)
Data gathering tools
Aimed to assess the level of depression, anxiety and stress in pregnant mothers, we used an online self-administered data gathering tool, so that the respondents feel more secure. The data gathering tool had three main parts: socio- demographic, obstetric and medical history, and the short form of Depression Anxiety Stress Scales (DASS-21).
The socio-demographic part comprised the participant’s age, marriage duration, residential area (Shiraz versus villages around Shiraz), educational level, employment status, insurance status, self-reported socioeconomic status (SES), and the perceived correlation between the household income and expenditure.
The second part included gestational age (GA), number of pregnancies including the current pregnancy, concurrent maternal comorbidities and medication history including the supplements.
The third part was DASS-21 questionnaire. This questionnaire was suggested by S. H. Lovibond and P. F. Lovibond as an acceptable substitution for DASS-42 in 1995 [15]. They applied DASS-21 in a sample of 2914 non-clinical individuals and showed that the internal consistency of Depression, Anxiety and Stress subscale was 0.91, 0.84 and 0.90, respectively. The validity and reliability of DASS-21 has been assessed by Asghari et al in a sample of 378 non-clinical Iranian population. They showed that DASS-21 had an acceptable Cronbach alpha for total score of DASS-21 (0.94) as well as for the subscales; including, 0.85 for Depression, 0.85 for Anxiety and 0.87 for Stress [16]. Also, Samani et al evaluated DASS-21 reliability in a sample of 638 Iranian university student [17]. They reported the internal consistency of Depression, Anxiety and Stress subscales 0.8, 0.76 and 0.77, respectively.
DASS-21 questionnaire consists of 21 questions, 7 in each subscale; depression (DASS-D), Anxiety (DASS-A) and Stress (DASS-S). Each question is scored through a 4-point Likert scale; 0 for “never”, 1 for “often”, 2 for “usually” and 3 for “always”. Hence, the score in each subscale ranges from 0 to 21, while the higher score represents the respondent’s higher level of stress, anxiety and stress. Score of DASS-D, DASS-A and DASS-S was considered abnormal if it was higher than 9, 7, and 14, respectively.
Statistical analysis
SPSS version 18.0 (IBM Corp., Armonk, NY, USA) was used for analysis of the data. Chi-square test was applied to assess the association between qualitative variables. Independent T test and ANOVA were used for comparing numeric variables between two groups and among three groups. Variables with p-values less than 0.2 in univariate analysis were entered into the logistic regression model and backward elimination (alpha-to-remove= 0.1) was used. P value less than 0. 05 was considered statistically significant.