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The Effect of Watching Cat Videos on Non-Stress Test Results And Stress Parameters in Pregnant Women

NCT07332039 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-01-25
Last updated
2026-02-11

Condition(s) studied

Maternal StressFetal Well-Being

Investigational drug(s) / intervention(s)

Group watching cat videosNon-Video Watching Group

Group watching cat videos: The cat video, which will be shown to pregnant women as part of the study, will be implemented as an intervention to reduce participants' stress levels during the NST. The NST session takes approximately 20 minutes, and the video will be played for this duration. The content of the video will be carefully selected to create a relaxing and entertaining effect on the audience. Participants will begin watching the video immediately after connecting to the NST device and will continue to watch throughout the NST. This process aims to calm participants, reduce stress levels, and promote overall relaxation.

Non-Video Watching Group: Participants randomly assigned to the control group will also rest for 10 minutes in a private room and all initial measurements will be taken.

Study summary

Pregnancy is a period in which women are physiologically and psychologically vulnerable, and the stress experienced can affect both maternal mental health and fetal well-being. The non-stress test (NST), used to assess fetal health in the final weeks of pregnancy, can cause anxiety in some women because it requires the mother to remain supine and immobile for extended periods. Prolonged testing or non-reactive results can also increase this stress. Therefore, simple methods are needed to reduce stress during NST. Humorous and cute content, especially animal videos, is known to promote positive emotions and psychological relaxation. This study evaluated the effects of watching cat videos during NST on stress levels and fetal physiological parameters in primiparous pregnant women.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Pregnant women who are primiparous, * Able to communicate in Turkish, * In their 34th-40th weeks of pregnancy, * Have no problems that would prevent them from viewing visual or auditory materials, * Have the cognitive ability to understand interactive video content, * Have not engaged in physical exercise for at least 2 hours prior to fetal heart rate monitoring will be included in the study. Exclusion Criteria: * Pregnant women with multiple pregnancies, * Uterine contractions detected during NST, * Diagnosed with a high-risk pregnancy (preeclampsia, gestational diabetes, placenta previa, etc.), * A phobia of cats (ailurophobia), * Pregnant women who became pregnant using assisted reproductive technologies (ART), * Have a history of a diagnosed endocrinological (e.g., hypothyroidism, hyperthyroidism, Cushing's syndrome) or psychiatric (e.g., anxiety disorder, depression) disease will be excluded from the study.

Primary outcome measure(s)

  • The effect of watching cat videos on stress parameters in pregnant women — This procedure will be performed during the NST for pregnant women experiencing their first pregnancy and who are between weeks 34 and 40 of gestation.
    Participants randomly assigned to the intervention group will be taken to a designated room determined by the researcher before the NST for their initial measurements. The "Pregnant Women Demographic Information Form" and the "State-Trait Anxiety Inventory (STAI Form TX-1)" will be administered. Blood pressure, heart rate, oxygen saturation, cortisol, and ACTH levels will be measured. All physiological measurements except ACTH and cortisol will be performed at three time points: before the NST (2 minutes before start), in the middle of the NST (approximately 10 minutes), and after the NST (2 minutes after completion). The "State-Trait Anxiety Inventory (STAI Form TX-1)" will also be administered after the NST. Following the NST, satisfaction levels will also be assessed using the Visual Analog Scale (VAS).

Trial sites (1)

FacilityCityRegionStatus
Istanbul University- Cerrahpasa Istanbul Turkey (Türkiye)
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07332039 on ClinicalTrials.gov ↗ ← All trials in Turkey