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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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05348954
Enrollment
88
Registered
2022-04-27
Start date
2023-05-05
Completion date
2024-06-02
Last updated
2024-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nurse's Role, Postpartum Disorder, Sexuality

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.

Interventions

OTHEREX-PLISSIT MODEL

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.

Sponsors

Gazi University
CollaboratorOTHER
Karamanoğlu Mehmetbey University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

Randomized controlled experimental study

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
EX-PLISSIT ModelEX-PLISSIT Model will be conducted to participants one weeks later after the first sessionThe 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-REVISEDThey will get an sexual health education and then their sexual disstress will be measured 4 weeks laterMeasuring sex-related personal distress for women
SEXUAL QUALITY OF LIFE SCALE-FEMALEThey will get an sexual health education and then their sexual quality of life will be measured 4 weeks laterThis scale measures the quality of sex life.

Countries

Turkey (Türkiye)

Contacts

Primary ContactNergiz Eryilmaz, Master
nergizeryilmaz@kmu.edu.tr+905458848830
Backup ContactAyten Şentürk Erenel, Prof

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026