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The Effect of Showing Fetal Images to High-Risk Pregnant Women on Stress and Sleep

NCT07260838 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2025-12-03

No results posted yet for this study

Summary

The study will be conducted to determine the effect of showing fetal images to high-risk pregnant women on pregnancy stress and sleep quality.

The study was conducted at Adana City Training and Research Hospital between November 2024 and May 2025 using a randomized controlled, interventional design. The sample of the study consisted of 35 intervention and 35 control group participants, totaling 70 individuals. Data were collected using the Personal Information Form, the Pregnancy Stress Rating Scale (PSRS-36) and the Richard-Campbell Sleep Scale. The intervention group was shown fetal images three times a day for two days; the control group received no intervention. The collected data were analyzed by comparing the pre-test and post-test scores. The data obtained from the study will be evaluated using SPSS IBM 24.0 package program in computer environment.

Research Hypotheses:

In the intervention and control groups; H0-1: Showing fetal images to high-risk pregnant women has no effect on pregnancy stress.

H0-2: Showing fetal images to high-risk pregnant women has no effect on sleep quality.

H1-1: Showing fetal images to high-risk pregnant women has an effect on pregnancy stress.

H1-2: Showing fetal images to high-risk pregnant women has an effect on sleep quality.

Conditions

  • Pregnancy, High-Risk

Interventions

OTHER

Showing fetal images

High-risk pregnant women in the intervention group were shown fetal images three times a day for two days.

Sponsors & Collaborators

  • Melike Nur SÖNMEZ

    lead OTHER

Principal Investigators

  • EVŞEN NAZİK, Professor · Çukurova University Faculty of Health Sciences

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-12-02
Primary Completion
2025-05-17
Completion
2025-05-19

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07260838 on ClinicalTrials.gov