NCT06735677

Brief Summary

The aim of this experimental study is to learn the effects of sexual health education during pregnancy on sexual myths, sexual function and quality of sexual life. The main question it aims to answer is: Is sexual health education effective in correcting sexual myths? Is sexual health education intervention effective in improving quality of sexual life? Is sexual health education intervention effective in improving sexual function? Participants who received the educational intervention prepared to improve quality of sexual life, sexual myths and sexual function will answer the survey questions after the completion of the training program.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
90

participants targeted

Target at P25-P50 for not_applicable pregnancy

Timeline
Completed

Started Feb 2023

Shorter than P25 for not_applicable pregnancy

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

February 1, 2023

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2023

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2023

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

December 6, 2024

Completed
10 days until next milestone

First Posted

Study publicly available on registry

December 16, 2024

Completed
Last Updated

December 16, 2024

Status Verified

December 1, 2024

Enrollment Period

5 months

First QC Date

December 6, 2024

Last Update Submit

December 11, 2024

Conditions

Keywords

Sexual mythsreproductive healthsexual attitudessexual health education

Outcome Measures

Primary Outcomes (2)

  • Sexual Quality of Life-Female

    Increase in sexual life quality scores at the end of the training program.

    4 weeks.

  • Female Sexual Function Index

    Increase in sexual function index scores at the end of the training program.

    4 weeks.

Study Arms (1)

Education

EXPERIMENTAL

These sessions covered reproductive health, sexual activity during pregnancy and the postpartum period, personal and sexual hygiene, domestic violence during pregnancy, and misconceptions about pregnancy.

Behavioral: sexual health education

Interventions

These sessions covered reproductive health, sexual activity during pregnancy and the postpartum period, personal and sexual hygiene, domestic violence during pregnancy, and misconceptions about pregnancy.

Education

Eligibility Criteria

Age18 Years - 49 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsFemale gender is suitable for participation in the study.
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • At least primary school graduate
  • Being in the 18-49 age group
  • Being pregnant

You may not qualify if:

  • Having a condition that prevents communication
  • Receiving hospital treatment during the data collection process

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kahramanmaraş Sütçü İmam University Faculty of Medicine Pregnant School

Kahramanmaraş, 46000, Turkey (Türkiye)

Location

MeSH Terms

Interventions

Sex Education

Intervention Hierarchy (Ancestors)

SexologyBehavioral SciencesBehavioral Disciplines and Activities

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Model Details: Data collection forms were administered to 100 pregnant women who attended the pregnancy school of a city hospital in a province of Türkiye and agreed to participate in the study. The participants were then randomly assigned by lot into intervention (n=50) and control (n=50) groups. Pregnant women in the intervention group received four training sessions over one month. These sessions covered reproductive health, sexual activity during pregnancy and the postpartum period, personal and sexual hygiene, domestic violence during pregnancy, and misconceptions about pregnancy. Following the completion of the training sessions, the Sexual Quality of Life-Female (SQOL-F) questionnaire and the Female Sexual Function Index (FSFI) were re-administered to all participants for final evaluation. Written informed consent was obtained from all participants before the study commenced. The study was completed with 90 participants (45 in the intervention group and 45 in the control group).
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Asst. Prof.

Study Record Dates

First Submitted

December 6, 2024

First Posted

December 16, 2024

Study Start

February 1, 2023

Primary Completion

June 30, 2023

Study Completion

December 31, 2023

Last Updated

December 16, 2024

Record last verified: 2024-12

Data Sharing

IPD Sharing
Will not share

Locations