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
Primary Purpose
Sexuality, Nurse's Role, Postpartum Disorder
Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
EX-PLISSIT MODEL
Sponsored by
About this trial
This is an interventional treatment trial for Sexuality
Eligibility Criteria
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
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Sexual dysfunction of women
Quality of sexual life
Arm Description
Sexual dysfunction of women
Quality of sexual life
Outcomes
Primary Outcome Measures
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.
THE FEMALE SEXUAL DISTRESS SCALE-REVISED
Measuring sex-related personal distress for women
SEXUAL QUALITY OF LIFE SCALE-FEMALE
This scale measures the quality of sex life.
Secondary Outcome Measures
Full Information
NCT ID
NCT05348954
First Posted
February 14, 2022
Last Updated
April 21, 2022
Sponsor
Karamanoğlu Mehmetbey University
Collaborators
Gazi University
1. Study Identification
Unique Protocol Identification Number
NCT05348954
Brief Title
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
Official Title
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
Study Type
Interventional
2. Study Status
Record Verification Date
April 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
May 2, 2022 (Anticipated)
Primary Completion Date
September 2, 2022 (Anticipated)
Study Completion Date
June 2, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karamanoğlu Mehmetbey University
Collaborators
Gazi University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sexuality, Nurse's Role, Postpartum Disorder
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled experimental study
Masking
Participant
Allocation
Randomized
Enrollment
88 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Sexual dysfunction of women
Arm Type
Experimental
Arm Description
Sexual dysfunction of women
Arm Title
Quality of sexual life
Arm Type
Experimental
Arm Description
Quality of sexual life
Intervention Type
Other
Intervention Name(s)
EX-PLISSIT MODEL
Intervention Description
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.
Primary Outcome Measure Information:
Title
EX-PLISSIT Model
Description
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.
Time Frame
EX-PLISSIT Model will be conducted to participants one weeks later after the first session
Title
THE FEMALE SEXUAL DISTRESS SCALE-REVISED
Description
Measuring sex-related personal distress for women
Time Frame
They will get an sexual health education and then their sexual disstress will be measured 4 weeks later
Title
SEXUAL QUALITY OF LIFE SCALE-FEMALE
Description
This scale measures the quality of sex life.
Time Frame
They will get an sexual health education and then their sexual quality of life will be measured 4 weeks later
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
The population of the study will be composed of women who are registered to family health centers determined by randomization in Karaman city center and who are in the 10 weeks-6 months postpartum period.
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nergiz Eryilmaz, Master
Phone
+905458848830
Email
nergizeryilmaz@kmu.edu.tr
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
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
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