NCT07332039

Brief 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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2026

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 8, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

January 12, 2026

Completed
13 days until next milestone

Study Start

First participant enrolled

January 25, 2026

Completed
8 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 2, 2026

Completed
3 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 5, 2026

Completed
Last Updated

February 11, 2026

Status Verified

January 1, 2026

Enrollment Period

8 days

First QC Date

December 8, 2025

Last Update Submit

February 9, 2026

Conditions

Keywords

Fetal Well-BeingMaternal StressCat Videos

Outcome Measures

Primary Outcomes (1)

  • The effect of watching cat videos on stress parameters in pregnant women

    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).

    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.

Secondary Outcomes (1)

  • The effect of watching cat videos on physiological parameters of the fetus

    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.

Study Arms (2)

Control Group

EXPERIMENTAL

Participants randomly assigned to the control group will also rest in a private room for 10 minutes, after which all initial measurements will be taken. A routine NST will then be performed.

Behavioral: Non-Video Watching Group

Intervention group

EXPERIMENTAL
Behavioral: Group watching cat videos

Interventions

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.

Intervention 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.

Control Group

Eligibility Criteria

Age18 Years+
Sexfemale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Istanbul University- Cerrahpasa

Istanbul, Turkey (Türkiye)

Location

Central Study Contacts

Rukiye Duman Research assistant

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
CARE PROVIDER
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Model Details: A Randomized Controlled Trial
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research assistant

Study Record Dates

First Submitted

December 8, 2025

First Posted

January 12, 2026

Study Start

January 25, 2026

Primary Completion

February 2, 2026

Study Completion

February 5, 2026

Last Updated

February 11, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Locations