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
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COMPLETED
NA
60 participants
INTERVENTIONAL
2024-11-18
2025-05-23
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
SUPPORTIVE_CARE
SINGLE
Study Groups
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Behavioral: sexual health counseling based on the BETTER model
Sexual health counseling based on the BETTER model
The content of the research will be discussed by face-to-face interviews with women who gave birth vaginally and applied to the hospital for birth control 8-10 weeks after delivery. Pre-evaluation forms will be applied to women who have agreed to participate in the study to evaluate the inclusion criteria. Women who meet the inclusion criteria will be divided into experimental-control groups using the block randomization method.
An appointment will be made for interviews with the women in the experimental group. It is planned that these meetings will be held in the form of online video calls and will last an average of 45 minutes. The final tests will be held 8 weeks after the online meetings are over.
Behavioral: sexual health counseling based on the BETTER model
The content of the research will be discussed by face-to-face interviews with women who gave birth vaginally and applied to the hospital for birth control 8-10 weeks after delivery. Pre-evaluation forms will be applied to women who have agreed to participate in the study to evaluate the inclusion criteria. Women who meet the inclusion criteria will be divided into experimental-control groups using the block randomization method.
An appointment will be made for interviews with the women in the experimental group. It is planned that these meetings will be held in the form of online video calls and will last an average of 45 minutes. The final tests will be held 8 weeks after the online meetings are over.
Control group: Routine postpartum care
Routine postpartum care
Women who gave birth vaginally and applied to the hospital for postpartum controls 8-10 weeks after delivery will be interviewed face-to-face with the women and the content of the research will be mentioned. Pre-evaluation forms will be applied to the women who accepted to participate in the study to evaluate the inclusion criteria. Women who meet the inclusion criteria will be divided into experimental-control groups using the block randomization method. Women in the control group will receive routine postpartum care administered in the hospital. Women in the control group will receive routine postpartum care administered in the hospital. Post-tests will be administered 8 weeks after the first interview.
No interventions assigned to this group
Interventions
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Behavioral: sexual health counseling based on the BETTER model
The content of the research will be discussed by face-to-face interviews with women who gave birth vaginally and applied to the hospital for birth control 8-10 weeks after delivery. Pre-evaluation forms will be applied to women who have agreed to participate in the study to evaluate the inclusion criteria. Women who meet the inclusion criteria will be divided into experimental-control groups using the block randomization method.
An appointment will be made for interviews with the women in the experimental group. It is planned that these meetings will be held in the form of online video calls and will last an average of 45 minutes. The final tests will be held 8 weeks after the online meetings are over.
Eligibility Criteria
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Inclusion Criteria
* Weeks of gestation 37 weeks and over,
* Who had a singleton pregnancy,
* Having a sexual partner/partner,
* Having started sexual intercourse before starting training,
* Without a diagnosed chronic disease (DM, HT, Heart disease, etc.),
* Labour week 37 weeks and over
* 18 years or older,
* Able to speak and understand Turkish,
Exclusion Criteria
* To have received training on sexual health and family planning in a hospital or other health institution other than discharge training,
18 Years
FEMALE
Yes
Sponsors
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Lokman Hekim University
OTHER_GOV
Responsible Party
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Nurgül ŞİMAL YAVUZ
Lecturer
Principal Investigators
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Nurgül ŞİMAL YAVUZ, Lecturer
Role: STUDY_DIRECTOR
Lokman Hekim University
Locations
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Lokman Hekim Etlik Hospital
Ankara, Keçiören, Turkey (Türkiye)
Countries
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Other Identifiers
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NSIMALYAVUZ
Identifier Type: -
Identifier Source: org_study_id
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