Video briefing before C-Section may lower stress hormones
NCT ID NCT07521592
First seen Jun 27, 2026 · Last updated Aug 27, 2026 · Updated 4 times
Summary
This study tests whether watching a short video about anesthesia and surgery before an elective C-section can lower anxiety and stress hormones (cortisol) more than standard verbal instructions from a doctor. 140 pregnant women will be randomly assigned to either video or verbal information. Researchers will measure anxiety with a questionnaire and cortisol from blood samples before and after the information session.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- video-based preoperative information
- What this could lead to
- If it works, hospitals could use simple videos to help calm women before planned C-sections, reducing stress without medication.
- What could go wrong
- This is a small, early-stage study (140 people) comparing two types of information delivery. The results may not apply to all hospitals or patients, and anxiety is complex—videos may not help everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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140 people
The number who actually took part.
- Started
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Apr 2026
- Finished
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Jul 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 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 * Ability to provide written informed consent Exclusion Criteria: * Emergency cesarean delivery * History of psychiatric disorders * Current use of anxiolytic or antidepressant medications * Endocrine disorders, particularly adrenal or thyroid disease * Current corticosteroid therapy * History of previous surgery under spinal anesthesia * Cognitive impairment preventing effective communication or completion of the assessment scales * American Society of Anesthesiologists (ASA) physical status III-V
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Elazığ Fethi Sekin City Hospital
Elâzığ, Lütfen Seçiniz., 23100, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a nasal spray make surgery less scary for kids?
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- Can simple recovery checklists after cesarean boost patient well-being?