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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

K

Karamanoğlu Mehmetbey University

Status

Enrolling

Conditions

Sexuality
Postpartum Disorder
Nurse's Role

Treatments

Other: EX-PLISSIT MODEL

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Full 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.

Enrollment

88 estimated patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

88 participants in 2 patient groups

Sexual dysfunction of women
Experimental group
Description:
Sexual dysfunction of women
Treatment:
Other: EX-PLISSIT MODEL
Quality of sexual life
Experimental group
Description:
Quality of sexual life
Treatment:
Other: EX-PLISSIT MODEL

Trial contacts and locations

1

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Central trial contact

Ayten Şentürk Erenel, Prof; Nergiz Eryilmaz, Master

Data sourced from clinicaltrials.gov

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