The Effect of Sex Education on Sexuality of Pregnant Women

Sponsor
NESLİHAN YILMAZ SEZER (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05790967
Collaborator
(none)
74
2
3.1

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Other: Sexual Education
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
74 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
The Effect of Sex Education on the Sexual Response and Attitudes Towards Sexuality of Pregnant Women
Anticipated Study Start Date :
Mar 27, 2023
Anticipated Primary Completion Date :
Jun 29, 2023
Anticipated Study Completion Date :
Jun 29, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Education Group

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.

No Intervention: CONTROL

Outcome Measures

Primary Outcome Measures

  1. Change in sexual response [baseline, four weeks later]

    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".

  2. Attitude Scale toward Sexuality during Pregnancy Change: [baseline, four weeks later]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • NESLİHAN YILMAZ SEZER

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
NESLİHAN YILMAZ SEZER, Faculty of Nursing, Ankara University
ClinicalTrials.gov Identifier:
NCT05790967
Other Study ID Numbers:
  • 20/189
First Posted:
Mar 30, 2023
Last Update Posted:
Mar 30, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Mar 30, 2023