Perception of ViolenceNCT06951529
The Effect of Reproductive Violence Education Given to Women on Perception of Violence, Conflict Resolution Styles and Awareness of Violence: A Randomized Controlled Trial
A study testing Reproductive violence education in people with Perception of Violence and Conflict Resolution Styles, run by Saglik Bilimleri Universitesi.
Trial summary
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. Read more about this study
- Who is it for?
- Any age, women only
- Conditions the study is for
- Perception of Violence, Conflict Resolution Styles
- What is being tested?
- Reproductive violence education
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 80 participants
- Where
- No sites listed yet
- Study dates
- 1 May 2025to 15 Sep 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- Women only
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- 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
Who cannot join
- Being in menopause
- Having a mental health problem that would prevent participation in the study
- Receiving psychiatric treatment
- Being an adolescent
Trial locations and contacts
No sites are listed yet.
About this study
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.
Read more
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.
- Conditions
- Perception of Violence, Conflict Resolution Styles
- Being tested
- Reproductive violence education
- Keywords
- violence, reproductive period, woman, midwifery
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Reproductive violence educationOther
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.
| Study group | Role | What they receive |
|---|---|---|
| No Intervention : control group (n:40) | No intervention | No intervention will be made to the control group. |
| Experimental : intervention group (n:40) | Experimental | 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. Receives: Other: Reproductive violence education |
What is being measured
The primary outcome is the main question the study is designed to answer.
Introductory Information Form
Women's age, socio-demographic characteristics, parameters related to violence are questioned. It will be created based on literature.
Measured: Baseline (10 mn)
Reproductive Violence Perception Form
It includes questions about physical, psychological, economic, sexual and emotional violence during the reproductive period.
Measured: Baseline (10 mn)
Conflict and violence awareness scale (CVV)
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.
Measured: Baseline (10 mn)
Secondary outcomes (2)
Reproductive Violence Perception Form
It includes questions regarding physical, psychological, economic, sexual and emotional violence applied during the reproductive period.
Measured: Post-test after training (10 mn)
Conflict and violence awareness scale (CVV)
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.
Measured: Post-test after training (10 mn)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted30 Apr 2025
- Study start1 May 2025 (estimated)
- Primary completion15 Jun 2025 (estimated)
- Study completion15 Sep 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Perception of ViolenceStudies of the same condition, open and under way.
- More trials run by Saglik Bilimleri UniversitesiThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 80 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Saglik Bilimleri Universitesi
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, YASEMİN AYDIN KARTAL, Saglik Bilimleri Universitesi
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06951529
- Sponsor's protocol ID
- SBU-AYDINKARTAL-ALEYNATEZ
- Status last verified
- Oct 2024
- First submitted
- 20 Mar 2025
- Last updated
- 30 Apr 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 30 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Reproductive Violence Education Given to Women on Perception of Violence, Conflict Resolution Styles and Awareness of Violence: A Randomized Controlled Trial
- ClinicalTrials.gov ID
- NCT06951529
- Acronym / sponsor ID
- SBU-AYDINKARTAL-ALEYNATEZ
- Conditions
- Perception of Violence, Conflict Resolution Styles
- Keywords
- violence, reproductive period, woman, midwifery
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 80 participants (estimated)
- Lead sponsor
- Saglik Bilimleri UniversitesiUniversity, hospital or other
- Study start
- 1 May 2025 (estimated)
- Primary completion
- 15 Jun 2025 (estimated)
- Study completion
- 15 Sep 2025 (estimated)
- First posted
- 30 Apr 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| No Intervention : control group (n:40) | No intervention | –No intervention will be made to the control group. |
| Experimental : intervention group (n:40) | Experimental | Other: Reproductive violence educationIn 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. |
Who may qualify
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (3 listed)
- 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
Key exclusion criteria (4 listed)
- Being in menopause
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Reproductive violence educationThe 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. | Other | Experimental : intervention group (n:40) |
Primary outcome
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.
Reproductive Violence Perception Form
Time frame: Baseline (10 mn)
It includes questions about physical, psychological, economic, sexual and emotional violence during the reproductive period.
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.
2 secondary outcomes
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)
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Apr 2025.
- Individual participant dataSharing planned: Yes
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Questions about this trial
What is this clinical trial studying?
A study testing Reproductive violence education in people with Perception of Violence and Conflict Resolution Styles, run by Saglik Bilimleri Universitesi.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 30 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Yasemin Aydın Kartal Prof. Dr. (0543 287 00 29, yasemin.aydin@sbu.edu.tr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Introductory Information Form (time frame: Baseline (10 mn)). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Apr 2025.