Effect of Video-Based Versus Verbal Preoperative Information on Anxiety and Cortisol Levels in Elective Cesarean Section

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorElazıg Fethi Sekin Sehir Hastanesi

About this trial

Preoperative anxiety is a common problem in patients undergoing elective cesarean section and may negatively affect perioperative outcomes through activation of the stress response, including increased cortisol levels. Effective preoperative information is considered a key non-pharmacological strategy to reduce anxiety; however, the optimal method of information delivery remains unclear. This prospective randomized controlled trial aims to compare the effects of video-based versus verbal preoperative information on anxiety levels and serum cortisol response in patients scheduled for elective cesarean delivery under spinal anesthesia. Anxiety will be assessed using the State-Trait Anxiety Inventory (STAI), and serum cortisol levels will be measured before and after the intervention. The findings of this study are expected to provide evidence for improving patient-centered preoperative education strategies in obstetric anesthesia."

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Pregnant women aged 18 years or older

Scheduled for elective cesarean delivery

Planned to receive spinal anesthesia

American Society of Anesthesiologists (ASA) physical status I-II

Disqualifiers

Emergency cesarean delivery

History of psychiatric disorders

Current use of anxiolytic or antidepressant medications

Endocrine disorders, particularly adrenal or thyroid disease

Trial design

Design model

Parallel

Treatments tested in this trial

  • Verbal Preoperative Information

    Behavioral

    Participants will receive standard preoperative information about anesthesia and the surgical procedure through face-to-face verbal communication delivered by an anesthesiologist according to routine clinical practice at least one hour before surgery.

  • Video-Based Preoperative Information

    Behavioral

    Participants will receive standardized video-based preoperative information covering anesthesia and the surgical procedure at least one hour before surgery. The content of the video will be equivalent to the verbal information provided in routine clinical practice.

Treatment groups

140 Participants
are divided into 2 treatment groups
Group A: Verbal Information GroupOther 1 intervention
Group B: Video-Based Information GroupOther 1 intervention

Trial outcomes

Primary outcomes

1

Change in preoperative anxiety level measured by the State-Trait Anxiety Inventory (STAI-S)

Change in preoperative anxiety level measured by the State-Trait Anxiety Inventory-State (STAI-S), a 20-item scale with scores ranging from 20 to 80, where higher scores indicate greater anxiety.

Time frame
Immediately before preoperative information and approximately 1 hour after preoperative information, before surgery

Secondary outcomes

1

Serum cortisol level change

Change in serum cortisol levels measured from venous blood samples obtained immediately before preoperative information and approximately 1 hour after preoperative information, before surgery.

Time frame
Immediately before preoperative information and approximately 1 hour after preoperative information, before surgery

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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