Role of Body Image in the Relationship Between Pregnant Women's Sexuality and Sexual Stress

NCT ID: NCT07132359

Last Updated: 2025-08-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

422 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-06-25

Study Completion Date

2025-03-15

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Sexual activity is negatively affected during pregnancy. In addition process of adapting to the changes in the pregnant woman's body negatively affects her psychology. Therefore, pregnant woman's perception of her body image can lead to sexual stress. This study aimed to determine the mediating role of body image perception in the relationship between pregnant women's attitudes toward sexuality and their sexual stress. The study sample consisted of 422 pregnant women.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Sexual activity is negatively affected during pregnancy. In addition process of adapting to the changes in the pregnant woman's body negatively affects her psychology. Therefore, pregnant woman's perception of her body image can lead to sexual stress. This study aimed to determine the mediating role of body image perception in the relationship between pregnant women's attitudes toward sexuality and their sexual stress. The study sample consisted of 422 pregnant women. Data collection tools included a "Personal Information Form," the "Attitude Scale toward Sexuality during Pregnancy," the "Female Sexual Distress Scale-Revised" and the "Body Understanding Measure for Pregnancy Scale."

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Women (Between 18 to 50 Years Old)

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

The Body Understanding Measure for Pregnancy Scale

During the study, the purpose of the study was explained to the pregnant women, and it was stated that participation in the study was completely voluntary and that they could leave the study at any time, and their written and verbal consent was obtained (Informed Consent Form). Pregnant women who agreed to participate in the study filled out the data collection forms individually.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Volunteering to participate in the study
* Having no communication problems
* Being at the ≥10th weeks of gestation
* Scoring ≥11.5 on the Female Sexual Distress Scale-Revised

Exclusion Criteria

* Refusing to participate in the study
* Having been diagnosed with a sexual dysfunction before pregnancy
* Having psychological health problems according to medical records
Minimum Eligible Age

20 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of Gaziantep

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Ece Kaplan

Asisstant Professor Obstetrics and Gynecology Nursing

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Gaziantep University

Gaziantep, , Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

References

Explore related publications, articles, or registry entries linked to this study.

Batuhan Karasin F, Yilmaz T. Psychometric properties of the Turkish version of BUMPs and its relationship with prenatal attachment. J Reprod Infant Psychol. 2025 Jan;43(1):62-75. doi: 10.1080/02646838.2023.2217718. Epub 2023 Jun 5.

Reference Type BACKGROUND
PMID: 37272411 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

GAUN-EBE-EKD-04

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

FETAL MOVEMENT COUNTING
NCT05361265 COMPLETED NA