The Effect of Sex Education on Sexuality of Pregnant Women - Trial NCT05790967
Access comprehensive clinical trial information for NCT05790967 through Pure Global AI's free database. This phase not specified trial is sponsored by NESLฤฐHAN YILMAZ SEZER and is currently Recruiting. The study focuses on Pregnancy. Target enrollment is 74 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.
Study Focus
Sponsor & Location
NESLฤฐHAN YILMAZ SEZER
Ankara University
Timeline & Enrollment
N/A
Mar 27, 2023
Jun 29, 2023
Primary Outcome
Change in sexual response,Attitude Scale toward Sexuality during Pregnancy Change:
Summary
Aim: In this study, it is aimed to determine the effect of sexual education given to pregnant
 women on attitudes towards sexuality and sexual response during pregnancy.
 
 The study will be carried out in two different groups. After the women are evaluated in terms
 of eligibility criteria for the research, the eligible pregnant women will be informed about
 the research and written informed consent will be obtained from those who accept. Random
 distribution of pregnant women to study groups will be made using the Block Randomization
 method. The following applications will be made to the groups.
 
 Education Group: Women in the experimental group will be given education on sexual life
 during pregnancy. Before the training, preliminary data will be collected and then the
 participants will be given two hours of individual and face-to-face training.
 
 At the end of the training, homework will be given to pregnant women to practice at home,
 including sharing their sexual feelings and thoughts with their spouse, sharing problems and
 concerns about sexuality during pregnancy, and using alternative ways other than sexual
 intercourse. In addition, a Sexual Life in Pregnancy Information Booklet will be given, and
 they will be asked to read the information in the booklet and share it with their spouses.
 After 4 weeks, the data sheets will be applied again.
 
 Control Group: Patients in the control group of the study will not be subjected to any
 treatment other than the routine procedure. Data collection forms will be applied to the
 patients in the control group at the beginning of the study and after 4 weeks.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT05790967
Non-Device Trial

