Clincosm LogoSign in Get a demo

The Effect of Sexual Counseling Based on PLISSIT Model to Women Undergoing Open Heart Surgery on Sexual Function and Sexual Quality of Life

Sponsor
Istanbul University-Cerrahpasa (Other)
Overall Status
Recruiting
CT.gov ID
NCT05260697
Collaborator
(none)
64
Enrollment
1
Location
2
Arms
16.5
Anticipated Duration (Months)
3.9
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This study is about sexual counseling after cardiac surgery; It can contribute to the counseling planning of nurses and other health professionals regarding sexual problems that may occur after surgery. Increasing the quality of life in the rehabilitation process after cardiac surgery and facilitating adaptation to life after surgery; but not enough.

Condition or Disease Intervention/Treatment Phase
  • Other: sexual counselling with plissit model
 N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
64 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Participant)
Primary Purpose:
Supportive Care
Official Title:
The Effect of Sexual Counseling Based on PLISSIT Model to Women Undergoing Open Heart Surgery on Sexual Function and Sexual Quality of Life
Actual Study Start Date :
Nov 16, 2020
Actual Primary Completion Date :
Dec 30, 2021
Anticipated Study Completion Date :
Apr 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Sexual Counselling Group

Sexual Counselling with PLISSIT model

Other: sexual counselling with plissit model
sexual counselling
No Intervention: Control Group

no intervention group

Outcome Measures

Primary Outcome Measures

  1. 'Female Sexual Function Index' scores will increase after sexual counseling based on the PLISSIT model will be given to individuals who will undergo open heart surgery. [1 year]

  2. After the sexual counseling based on the PLISSIT model to be given to the individuals who will undergo open heart surgery, the scores of the "Sexual Quality of Life Scale-Female Form" will increase. [1 year]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:

  • Volunteering to participate in the research

  • 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:

  • Unwillingness to participate in the research

  • 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Merve TUNCER İstanbul Turkey

Sponsors and Collaborators

  • Istanbul University-Cerrahpasa

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Merve Tuncer, Lecturer, Istanbul University-Cerrahpasa
ClinicalTrials.gov Identifier:
NCT05260697
Other Study ID Numbers:
  • 13022260-302.14.05
First Posted:
Mar 2, 2022
Last Update Posted:
Mar 2, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Mar 2, 2022