The Effect of Sexual Counseling Based on PLISSIT Model to Women Undergoing Open Heart Surgery on Sexual Function and Sexual Quality of Life
NCT ID: NCT05260697
Last Updated: 2022-03-02
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.
UNKNOWN
NA
64 participants
INTERVENTIONAL
2020-11-16
2022-04-01
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 Counselling Based on PLISSIT and BETTER Model After Hysterectomy
NCT06609096
The Effect of EX-PLISSIT Model-Based Sexual Counseling in Postmenopausal Women
NCT07283146
The Effect of Sexual Counseling Given According to the PLISSIT Model on FSFI, MAS and SQOL-F of Postmenopausal Women
NCT05448079
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
NCT05348954
Sexual Counseling's Impact on Hip Replacement Patients' Sexual Function and Quality of Life: a PLISSIT Model Study
NCT06017128
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
CROSSOVER
SUPPORTIVE_CARE
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Sexual Counselling Group
Sexual Counselling with PLISSIT model
sexual counselling with plissit model
sexual counselling
Control Group
no intervention group
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
sexual counselling with plissit model
sexual counselling
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Being a woman
* Being over 18 years old
* Willingness to undergo open heart surgery
* Euroscore score ≤ 6 (low mortality risk due to cardiac surgery)
* Being sexually active
* Absence of sexual health problems in the spouse
* Ability to communicate verbally and be literate
* Women without neurological or psychiatric disorders
* Knowing Turkish
Exclusion Criteria
* Euroscore score \>6 (high risk of mortality)
* Not being sexually active
* Having a diagnosed sexual health problem in the spouse
* Women with neurological and psychiatric disorders
18 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Istanbul University - Cerrahpasa
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Merve Tuncer
Lecturer
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Merve TUNCER
Istanbul, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
References
Explore related publications, articles, or registry entries linked to this study.
Tuncer M, Yesiltepe Oskay U. Effect of sexual counseling on sexual function and sexual quality of life for women undergoing open heart surgery: a pilot randomized controlled trial. J Sex Med. 2023 Jun 28;20(7):1010-1017. doi: 10.1093/jsxmed/qdad065.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
13022260-302.14.05
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.