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The Effect of Reproductive Violence Education Given to Women on Perception of Violence, Conflict Resolution Styles and Awareness of Violence: A Randomized Controlled Trial

S

Saglik Bilimleri Universitesi

Status

Not yet enrolling

Conditions

Conflict Resolution Styles
Perception of Violence

Treatments

Other: Reproductive violence education

Study type

Interventional

Funder types

Other

Identifiers

NCT06951529
SBU-AYDINKARTAL-ALEYNATEZ

Details and patient eligibility

About

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.

Enrollment

80 estimated patients

Sex

Female

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

80 participants in 2 patient groups

No Intervention : control group (n:40)
No Intervention group
Description:
No intervention will be made to the control group.
Experimental : intervention group (n:40)
Experimental group
Description:
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.
Treatment:
Other: Reproductive violence education

Trial contacts and locations

0

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Central trial contact

Aleyna Bulut Ress. Ass, Res. Ass; Yasemin Aydın Kartal Prof. Dr.

Data sourced from clinicaltrials.gov

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