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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05790967
Other study ID # 20/189
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 27, 2023
Est. completion date June 29, 2023

Study information

Verified date November 2023
Source Ankara University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 74
Est. completion date June 29, 2023
Est. primary completion date June 29, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Primigravida - Having a singleton pregnancy - Being between 14 -22 weeks of pregnancy - Living with their partner Exclusion Criteria: - Pregnant woman or her partner has a previous diagnosis of sexual dysfunction - Having a risky situation where sexual intercourse is prohibited during pregnancy by the physician - Use of psychiatric drugs - Pregnant woman or her partner has a previous diagnosis of sexual dysfunction - Having a risky situation where sexual intercourse is prohibited during pregnancy by the physician - Use of psychiatric drugs such as antidepressants

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Sexual Education
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.

Locations

Country Name City State
Turkey Ankara University Cebeci Hospital Ankara Mamak

Sponsors (1)

Lead Sponsor Collaborator
NESLIHAN YILMAZ SEZER

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in sexual response Pregnancy Sexual Response Inventory which evaluates sexual activity and sexuality problems in pregnant women, consists of two parts and a total of 38 items. The total score ranges from 0 to 100, with scores between 0-25 as "Very bad", between 25-50 as "Bad", between 50-75 as "Good" and between 75-100 as "Excellent". baseline, four weeks later
Primary Attitude Scale toward Sexuality during Pregnancy Change: Attitude towards Sexuality in Pregnancy consists of 34 items and 3 sub-dimensions. The increase in the total score obtained from the scale indicates that the attitudes towards sexuality during pregnancy are positive, and the decrease in the total score indicates that the attitudes towards sexuality during pregnancy are negative. In addition, the cut-off point of the scale was determined as 111.5. baseline, four weeks later
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