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Clinical Trials/NCT05348954
NCT05348954
Recruiting
Not Applicable

Determining the Effects of Sexual Health Education and Counseling Given to Women in the Postpartum Period Based on the EX-PLISSIT Model on Sexual Life

Karamanoğlu Mehmetbey University1 site in 1 country88 target enrollmentMay 5, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sexuality
Sponsor
Karamanoğlu Mehmetbey University
Enrollment
88
Locations
1
Primary Endpoint
EX-PLISSIT Model
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The aim of this study will be to determine the effect of the sexual health education and counseling program, which is given to women in the postpartum period based on the Ex-PLISSIT model, on women's sexual life, including sexual function, sexual distress and sexual life quality.

Detailed Description

The study is a multicenter, parallel randomized controlled experimental study with block randomization.For the determination of the working groups, the researcher; will give general information about the research to women who have applied to the family health center and meet the inclusion criteria in the postpartum period of 10 weeks-6 months and agree to participate, and will receive their written and verbal consent for participation.

Registry
clinicaltrials.gov
Start Date
May 5, 2023
End Date
June 2, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Karamanoğlu Mehmetbey University
Responsible Party
Principal Investigator
Principal Investigator

Nergiz Eryilmaz

Principal Investigator

Karamanoğlu Mehmetbey University

Eligibility Criteria

Inclusion Criteria

  • Being primiparous
  • Having given birth at 38-42 weeks of gestation,
  • Having a single birth,
  • Not experiencing any postpartum complications
  • The time elapsed from birth is between 10 weeks and 6 months
  • Being sexually active
  • Having a spouse/partner
  • Having a smartphone or computer with a camera
  • Being at least literate

Exclusion Criteria

  • A previous sexual function of the woman herself or her husband.
  • Having a chronic disease that she expresses herself (such as cardiovascular disease, hypertension, etc.)
  • Having a health problem that requires the baby to be hospitalized
  • Having received sexual education/counselling
  • Spouse or self-diagnosed mental problem
  • Having a diagnosis that will affect sexual function or body image, such as mastectomy

Outcomes

Primary Outcomes

EX-PLISSIT Model

Time Frame: EX-PLISSIT Model will be conducted to participants one weeks later after the first session

The content of the program will include information about the anatomy and physiology of the male-female reproductive system, sexuality and sexual cycle physiology, factors affecting sexuality, postpartum changes, hormonal changes, breastfeeding and their effects on sexuality, and methods of contraception.

THE FEMALE SEXUAL DISTRESS SCALE-REVISED

Time Frame: They will get an sexual health education and then their sexual disstress will be measured 4 weeks later

Measuring sex-related personal distress for women

SEXUAL QUALITY OF LIFE SCALE-FEMALE

Time Frame: They will get an sexual health education and then their sexual quality of life will be measured 4 weeks later

This scale measures the quality of sex life.

Study Sites (1)

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