Anxiety. Anxiety
Conditions
Interventions
Intervention 1: This study is done on two groups, one intervention group attending in the training sessions and one control group that no specific action is performed for them.Intervention Group: Init
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Willingness to enter the study Cesarean section operation (for reasons including previous cesarean sections, medical conditions, abnormalities of the placenta such as placenta praevia, and abnormal position of the fetus such as breech position) Having a gestational age of 34 weeks or more No history of anxiety and mental illness (if patients take anti-depressant or sedative medications on a regular basis, they are not included in the study) No history of chronic and cancerous pains Multigravida women
Exclusion criteria
Exclusion criteria: No willingness to participate in the research In case of any complications during surgery and anesthesia, they will be excluded from the study In case of the emergency cesarean section, the patient will be excluded from the study In the case of preterm delivery, they will be excluded from the study In the case of having a classic scar from the previous cesarean section, the patient will be excluded from the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Anxiety score and physiological parameters (including blood pressure, breathing rhythm, blood oxygen saturation, and heart rate) in pregnant mothers before participating in educational classes. Timepoint: Before participating in educational classes. Method of measurement: Anxiety score by completing the Beck anxiety questionnaire and physiological parameters using pertained tools. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNeda Hatami
Shiraz University of Medical Sciences
Outcome results
None listed