Study Results
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.
COMPLETED
NA
90 participants
INTERVENTIONAL
2023-02-01
2023-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Sexual dysfunction in women is a complex problem affected by many biological, psychological and individual factors. It is stated that sexual dysfunction in women is a common problem that increases with age and affects 30% to 50% of women, but it is known that its prevalence is quite high among young women.
Sexual life quality can be defined as the individual's perception of their own sexual life in a culture and value system according to their personal goals, expectations, criteria and earnings. Almost all sexual myths consist of negative attitudes such as sexual intercourse during pregnancy being harmful, and these attitudes also negatively affect the quality of sexual life.
By receiving consultancy services on how to have sexual life during pregnancy and obtaining information from the right sources, the prevalence of sexual myths during pregnancy will decrease and the effect on the quality of sexual life during pregnancy will be minimized.
This study aims to provide training to the target group of pregnant women on issues such as reproductive health, changes that may occur due to pregnancy, sexual activity during pregnancy and the postpartum period, and hygiene. The aim of these trainings is to inform pregnant women about sexual health and to increase the quality of their sexual life.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Education
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.
sexual health education
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.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
sexual health education
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.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Being in the 18-49 age group
* Being pregnant
Exclusion Criteria
* Receiving hospital treatment during the data collection process
18 Years
49 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Amasya University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Zehra Incedal Sonkaya
Asst. Prof.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Kahramanmaraş Sütçü İmam University Faculty of Medicine Pregnant School
Kahramanmaraş, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
182213
Identifier Type: -
Identifier Source: org_study_id