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NCT Number: NCT06951529

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

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.

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Key information

Conditions

Perception of Violence Conflict Resolution Styles

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Reproductive violence education

Other

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 outcomes

  1. Introductory Information Form

    Time frame: Baseline (10 mn)

    Women's age, socio-demographic characteristics, parameters related to violence are questioned. It will be created based on literature.

  2. Reproductive Violence Perception Form

    Time frame: Baseline (10 mn)

    It includes questions about physical, psychological, economic, sexual and emotional violence during the reproductive period.

  3. Conflict and violence awareness scale (CVV)

    Time frame: Baseline (10 mn)

    It was developed by the Ohio Education Commission in 2002 and its validity and reliability study was conducted by Sargin in 2010. CSFQ, which can be applied to adolescents and adults, is a five-point scale containing 27 categorical symptom items. (1. Strongly disagree, 2. Disagree, 3. Partially agree, 4. Agree, 5. Strongly agree). There is no reversed item. The high score obtained from the total of the items in the scale indicates that the individual has a high level of awareness regarding conflict and violence. The min-max score range of the CSFQ scale is 27-135. The internal consistency coefficient of the scale was found to be 0.87.

Secondary outcomes

  1. Reproductive Violence Perception Form

    Time frame: Post-test after training (10 mn)

    It includes questions regarding physical, psychological, economic, sexual and emotional violence applied during the reproductive period.

  2. Conflict and violence awareness scale (CVV)

    Time frame: Post-test after training (10 mn)

    It was developed by the Ohio Education Commission in 2002 and its validity and reliability study was conducted by Sargin in 2010. CSFQ, which can be applied to adolescents and adults, is a five-point scale containing 27 categorical symptom items. (1. Strongly disagree, 2. Disagree, 3. Partially agree, 4. Agree, 5. Strongly agree). There is no reversed item. The high score obtained from the total of the items in the scale indicates that the individual has a high level of awareness regarding conflict and violence. The min-max score range of the CSFQ scale is 27-135. The internal consistency coefficient of the scale was found to be 0.87.

Other outcomes

  1. Reproductive Violence Perception Form

    Time frame: 4 weeks after training (10 mn)

    It includes questions regarding physical, psychological, economic, sexual and emotional violence applied during the reproductive period.

  2. Conflict and violence awareness scale (CVV)

    Time frame: 4 weeks after training (10 mn)

    It was developed by the Ohio Education Commission in 2002 and its validity and reliability study was conducted by Sargin in 2010. CSFQ, which can be applied to adolescents and adults, is a five-point scale containing 27 categorical symptom items. (1. Strongly disagree, 2. Disagree, 3. Partially agree, 4. Agree, 5. Strongly agree). There is no reversed item. The high score obtained from the total of the items in the scale indicates that the individual has a high level of awareness regarding conflict and violence. The min-max score range of the CSFQ scale is 27-135. The internal consistency coefficient of the scale was found to be 0.87.

Study contacts

Contact information is provided by the study sponsor or research team.

Aleyna Bulut Ress. Ass, Res. Ass

CONTACT

[email protected]

0536 562 61 84

Yasemin Aydın Kartal Prof. Dr.

CONTACT

[email protected]

0543 287 00 29

Sponsors and collaborators

Lead sponsor

Saglik Bilimleri Universitesi

Other

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Apr 30, 2025
Registry last updated
Apr 30, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.