The Effect of Reproductive Violence Education Given to Women on Perception of Violence, Conflict Resolution Styles and Awareness of Violence: A Randomized Controlled Trial
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Reproductive violence education.
- Who it may be relevant to
- Registry conditions: Perception of Violence, Conflict Resolution Styles. Basic parameters: No limits · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
This study was planned as a methodological and randomized controlled experimental study to determine the effects of reproductive violence education given to women on women's perceptions of violence. H0a: There is no difference in the perception levels of reproductive violence between women who were given and those who were not given reproductive violence education. 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.
Interventions
- Other 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.
Primary outcome measures
- Introductory Information Form [Time frame: Baseline (10 mn)]
- Reproductive Violence Perception Form [Time frame: Baseline (10 mn)]
- Conflict and violence awareness scale (CVV) [Time frame: Baseline (10 mn)]
Secondary outcome measures (2)
- Reproductive Violence Perception Form [Time frame: Post-test after training (10 mn)]
- Conflict and violence awareness scale (CVV) [Time frame: Post-test after training (10 mn)]
Eligibility criteria
Inclusion criteria
- Being literate
- 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
- Being in menopause
- Having a mental health problem that would prevent participation in the study
- Receiving psychiatric treatment
- Being an adolescent
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Health services research
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06951529 · SBU-AYDINKARTAL-ALEYNATEZ