The study will be carried out in two different groups. Participants will be approached after being hospitalized for at least 24 hours. After the pregnant women are evaluated in terms of eligibility criteria for the research, the pregnant women who are eligible will be informed about the research and written informed consent will be obtained from the pregnant women who accept. The random distribution of pregnant women to the study groups will be carried out random.
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Change in anxiety
Timeframe: at the beginning of the study, 3 days later
Change in Depression
Timeframe: at the beginning of the study, 3 days later
Change in Sleep Quality
Timeframe: at the beginning of the study, 3 days later