About this trial
This prospective randomized controlled trial aims to evaluate the effects of verbal and video-based preoperative education on anxiety levels and serum cortisol response in women scheduled for elective cesarean delivery under spinal anesthesia.
Eligible participants will be randomly assigned to receive either standard verbal education or a standardized video-based educational intervention before surgery. Anxiety levels will be assessed using the State-Trait Anxiety Inventory (STAI-S), and serum cortisol levels will be measured before and after the educational intervention.
The primary objective is to compare the effectiveness of the two educational methods in reducing preoperative anxiety and physiological stress response.
Eligibility criteria
Qualifiers
Female participants aged 18 years or older
Scheduled for elective cesarean delivery
Planned to undergo spinal anesthesia
American Society of Anesthesiologists (ASA) physical status I or II
Disqualifiers
Emergency cesarean delivery
History of psychiatric disease
Current use of anxiolytic or antidepressant medications
Endocrine disorders, including adrenal or thyroid disease
Trial design
Treatments tested in this trial
- Video-Based Preoperative Education
- Verbal Preoperative Education