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
NCT ID: NCT05348954
Last Updated: 2024-02-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
88 participants
INTERVENTIONAL
2023-05-05
2024-06-02
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Effect of Sexual Education-Counseling According to PLISSIT Model of Couples' Sexual Functions During Pregnancy and Postpartum
NCT06762301
The Effect of Sexual Education Based on the PLISSIT Model on Sexual Function, Attitudes Towards Sexuality and Sexual Distress in Pregnant Women
NCT06530108
The Effect of Postpartum Contraceptive Method Counselling on the Intention to Use Family Planning Methods
NCT07119554
The Effect of Sexual Counseling Based on PLISSIT Model to Women Undergoing Open Heart Surgery on Sexual Function and Sexual Quality of Life
NCT05260697
Sexual Education in Women Based On The Plissit Model On Awareness And Attitude in Midwifery Students
NCT05967104
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Sexual dysfunction of women
Sexual dysfunction of women
EX-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.
Quality of sexual life
Quality of sexual life
EX-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.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
EX-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.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* 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
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Gazi University
OTHER
Karamanoğlu Mehmetbey University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Nergiz Eryilmaz
Principal Investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Karaman Halk Sağlığı Müdürlüğü
Karaman, Merkez, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Ayten Şentürk Erenel, Prof
Role: CONTACT
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
study1
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.