- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07049510
- Original Trial
Combating Violence Against Women
The Effect of the Programme on Combating Violence Against Women on Domestic Violence Awareness and Gender Attitudes: A Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Personal Information Form, Domestic Violence Awareness Scale and Gender Role Attitude Scale will be used in collecting research data.
After the Personal Information Form, Domestic Violence Awareness Scale and Gender Role Attitude Scale are applied to all women as a pre-test, the women in the experimental group will be included in the Combating Violence Against Women program. The program will be given in 4 sessions in 1 day. Demonstration, powerpoint, feedback and brainstorming methods will be used in the training.
No intervention will be made to the control group.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Çorum, Turkey
- Ordu University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Women between the ages of 18-45,
- Who speaks Turkish,
- Who has previously applied to law enforcement due to violence,
- Women who volunteer to participate in the research.
Exclusion Criteria:
- Women diagnosed with a psychiatric illness.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Active Comparator: Control group
All women will be given the Personal Information Form, Domestic Violence Awareness Scale and Gender Role Attitude Scale as a pre-test.
No intervention will be made to the control group.
After 8 weeks, all women will be reunited and given the Domestic Violence Awareness Scale and Gender Role Attitude Scale as a post-test.
|
After the Personal Information Form, Domestic Violence Awareness Scale and Gender Role Attitude Scale are applied to all women as a pre-test, the women in the experimental group will be included in the Combating Violence Against Women program. The program will be given in 4 sessions in 1 day. Demonstration, powerpoint, feedback and brainstorming methods will be used in the training. 8 weeks after the completion of the training, all women will be reunited and the Domestic Violence Awareness Scale and Gender Role Attitude Scale will be applied as a post-test. |
|
Experimental: Combating violence against women
After the Personal Information Form, Domestic Violence Awareness Scale and Gender Role Attitude Scale are applied to all women as a pre-test, the women in the experimental group will be included in the Combating Violence Against Women program. The program will be given in 4 sessions in 1 day. Demonstration, powerpoint, feedback and brainstorming methods will be used in the training. 8 weeks after the completion of the training, all women will be reunited and the Domestic Violence Awareness Scale and Gender Role Attitude Scale will be applied as a post-test. |
After the Personal Information Form, Domestic Violence Awareness Scale and Gender Role Attitude Scale are applied to all women as a pre-test, the women in the experimental group will be included in the Combating Violence Against Women program. The program will be given in 4 sessions in 1 day. Demonstration, powerpoint, feedback and brainstorming methods will be used in the training. 8 weeks after the completion of the training, all women will be reunited and the Domestic Violence Awareness Scale and Gender Role Attitude Scale will be applied as a post-test. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Domestic Violence Awareness Scale
Time Frame: 2 months
|
The scale developed by Özyürek and Kurnaz (2019) consists of 20 items measuring awareness of domestic violence on a three-point Likert scale.
The highest score that can be obtained from each item is three, and the lowest score is one.
Items 1-5 in the scale constitute the sub-dimensions of "Definition of Domestic Violence", items 6-10 constitute the sub-dimensions of "Consequences of Domestic Violence", items 11-15 constitute the sub-dimensions of "Acceptance of Domestic Violence", and items 16-20 constitute the sub-dimensions of "Normalization of Domestic Violence".
High total scores obtained from the entire scale can be interpreted as the individual having views compatible with the expected behaviors and attitudes in scientific and legal fields in interpreting domestic violence and having a high level of awareness of domestic violence.
The Cronbach alpha coefficient of the scale was reported to be 0.92 and ranged between 0.71 and 0.92 for its sub-dimensions.
In this study, Cronbach
|
2 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Gender Roles Attitude Scale
Time Frame: 2 months
|
Gender Roles Scale was originally developed by García-Cueto and colleagues (2015).
Adaptation of the scale to Turkish and reliability validity study were conducted by Bakioğlu and Türküm (2019).
In the original study, Cronbach alpha internal consistency coefficient was calculated as 0.99 within the scope of reliability of the scale, in the adaptation study, Cronbach alpha internal consistency coefficient was calculated as 0.88 and test-retest reliability was calculated as 0.77.
The scale consists of 15 questions and a single dimension.
The items are answered in Likert type as 1= I completely disagree, 2= I disagree, 3= I am undecided, 4= I agree, 5= I completely agree and so on.
The 13 items of the scale, except for items 1 and 2, are reverse coded.
A total score is obtained from the scale, and a higher score indicates a higher negative attitude towards gender roles.
In other words, a person who scores high on the scale adopts gender roles less and shows less commitment than a person
|
2 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Combating Violence Against Wom
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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