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The Effect of Sex Education on Sexuality of Pregnant Women

N

NESLİHAN YILMAZ SEZER

Status

Completed

Conditions

Pregnancy

Treatments

Other: Sexual Education

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

74 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

74 participants in 2 patient groups

Education Group
Experimental group
Treatment:
Other: Sexual Education
CONTROL
No Intervention group

Trial contacts and locations

1

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Central trial contact

Faik Acar Koç, Prof

Data sourced from clinicaltrials.gov

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