Sexual Health Education Given to Women

NCT ID: NCT07037602

Last Updated: 2025-06-25

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

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Recruitment Status

ENROLLING_BY_INVITATION

Clinical Phase

NA

Total Enrollment

66 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-05-29

Study Completion Date

2025-09-20

Brief Summary

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No study was found in the literature examining the effects of sexual health education on sexual myths and self-consciousness. The aim of the study was to investigate the effects of sexual health education on sexual myths and self-consciousness in women.

Detailed Description

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Sexual myths can be defined as false, stereotyped judgments that individuals believe to be true about sexuality, are generally exaggerated, have no scientific basis, and limit the freedom to live sexuality. Sexual myths are widely seen in society and can vary between cultures and societies, and even between individuals. Especially in closed-structure societies, these myths are increasingly widespread by being passed down from generation to generation. Sexual myths can cause people to have unrealistic expectations, feel inadequate due to these expectations, and feel anxious. As a result of all these, sexual dysfunctions can occur, and the treatment process can be negatively affected in people with sexual dysfunction. If sexual self-consciousness, that is, sexuality, has not yet been discovered as a personal area, if the person's idea of what to expect from sexual contact is shaped by myths, their sexual health may deteriorate. It is known that the most important factors that pave the way for sexual myths are lack of sexual education and information, the inability to openly discuss and discuss issues related to sexuality within the family, schools or society, and the inability to benefit from sufficient scientific research and publications.

Conditions

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Nursing

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

SINGLE

Participants

Study Groups

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Control group

All women will be given the Personal Information Form, Sexual Myths Scale and Sexual Self-Consciousness Scale as a pre-test. No intervention will be made to the control group. After 8 weeks, the women will be reunited and given the Sexual Myths Scale and Sexual Self-Consciousness Scale as a post-test.

Group Type ACTIVE_COMPARATOR

No Interventions

Intervention Type OTHER

No intervention will be made.

sexual health education

After the Personal Information Form, Sexual Myths Scale and Sexual Self-Awareness Scale are applied as a pre-test to all women, sexual health training will be given to the women in the experimental group. The training will be given in 4 sessions over 2 weeks. Demonstration, powerpoint, feedback and brainstorming methods will be used in the training.

Group Type EXPERIMENTAL

Sexual Health Education

Intervention Type OTHER

After the Personal Information Form, Sexual Myths Scale and Sexual Self-Awareness Scale are applied as a pre-test to all women, sexual health training will be given to the women in the experimental group. The training will be given in 4 sessions over 2 weeks. Demonstration, powerpoint, feedback and brainstorming methods will be used in the training.

Interventions

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Sexual Health Education

After the Personal Information Form, Sexual Myths Scale and Sexual Self-Awareness Scale are applied as a pre-test to all women, sexual health training will be given to the women in the experimental group. The training will be given in 4 sessions over 2 weeks. Demonstration, powerpoint, feedback and brainstorming methods will be used in the training.

Intervention Type OTHER

No Interventions

No intervention will be made.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Women between the ages of 18-45,
* Those who have not received sexual health education before,
* Those who speak Turkish,
* Women who volunteer to participate in the research.

Exclusion Criteria

* Those who have been medically diagnosed with sexual dysfunction,
* Women diagnosed with a psychiatric illness.
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Hitit University

OTHER

Sponsor Role lead

Responsible Party

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Fatma Yildirim

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Ordu University

Ordu, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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Sexual Health Education

Identifier Type: -

Identifier Source: org_study_id

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