The Effect of Reproductive Violence Education Given to Women on Perception of Violence, Conflict Resolution Styles and Awareness of Violence: A Randomized Controlled Trial
NCT ID: NCT06951529
Last Updated: 2025-04-30
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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NOT_YET_RECRUITING
NA
80 participants
INTERVENTIONAL
2025-05-01
2025-09-15
Brief Summary
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H1a: There is a difference in the perception levels of reproductive violence between women who were given and those who were not given reproductive violence education.
H0b: There is no difference in the conflict resolution styles and violence awareness levels between women who were given and those who were not given reproductive violence education.
H1b: There is a difference in the conflict resolution styles and violence awareness levels between women who were given and those who were not given reproductive violence education.
In the second phase of the study, 4 hours of reproductive violence education will be given to women in the intervention group and brochures on reproductive violence will be distributed. The education will be held in the meeting hall of Hamidiye Faculty of Health Sciences in the form of a powerpoint presentation and case discussion. Before the training, the "Informed Consent Form", "Introductory Information Form", "Reproductive Violence Perception Form/Scale" and "Conflict and Violence Awareness Scale" will be applied to the intervention group. After the training, the "Reproductive Violence Perception Form/Scale" and "Conflict and Violence Awareness Scale" will be applied. As a follow-up test, the "Reproductive Violence Perception Form/Scale" and "Conflict and Violence Awareness Scale" will be applied after 4-6 weeks.
Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
SINGLE
Study Groups
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No Intervention : control group (n:40)
No intervention will be made to the control group.
No interventions assigned to this group
Experimental : intervention group (n:40)
In the second phase of the study, women in the intervention group will receive a 4-hour training on reproductive violence and brochures on reproductive violence will be distributed. The training will be given in the form of a powerpoint presentation and case discussion in the meeting hall of the Hamidiye Faculty of Health Sciences. Before the training, the "Informed Voluntary Consent Form", "Introductory Information Form", "Reproductive Violence Perception Form/Scale" and "Conflict and Violence Awareness Scale" will be applied to the intervention group. After the training, the "Reproductive Violence Perception Form/Scale" and "Conflict and Violence Awareness Scale" will be applied. As a follow-up test, the "Reproductive Violence Perception Form/Scale" and "Conflict and Violence Awareness Scale" will be applied after 4-6 weeks.
Reproductive violence education
The training content, which was created by obtaining expert opinions based on literature, will cover the violence that women are exposed to or may be exposed to according to the cycles they experience during their reproductive years. Definition of Violence and Its Effects on Women's Health, Adolescence and Menstruation Period Violence, Family Planning and Infertility Violence, Pregnancy and Birth-Related Violence, Menopause-Related Violence, Legal Processes in Combating Reproductive Violence.
Interventions
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Reproductive violence education
The training content, which was created by obtaining expert opinions based on literature, will cover the violence that women are exposed to or may be exposed to according to the cycles they experience during their reproductive years. Definition of Violence and Its Effects on Women's Health, Adolescence and Menstruation Period Violence, Family Planning and Infertility Violence, Pregnancy and Birth-Related Violence, Menopause-Related Violence, Legal Processes in Combating Reproductive Violence.
Eligibility Criteria
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Inclusion Criteria
* Being a volunteer to participate in the research
* Being a female administrative staff other than academic staff working within the Health Sciences University Hamidiye Complex
Exclusion Criteria
* Having a mental health problem that would prevent participation in the study
* Receiving psychiatric treatment
* Being an adolescent
FEMALE
No
Sponsors
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Saglik Bilimleri Universitesi
OTHER
Responsible Party
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YASEMİN AYDIN KARTAL
Prof. Dr.
Central Contacts
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Other Identifiers
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SBU-AYDINKARTAL-ALEYNATEZ
Identifier Type: -
Identifier Source: org_study_id