- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06408831
The Effect of Web-Based Cyber Sexual Violence Training on Cyber Sexual Violence Experience, Sensitivity and Security
May 7, 2024 updated by: Sehadet, Inonu University
The Effect of Web-Based Cyber Sexual Violence Training and Consultancy on Cyber Sexual Violence Experience, Sensitivity and Cyber Security
The aim of this study is to provide web-based cyber sexual violence training with a model (Knowledge, Motivation, Behavior Skills (IMB) Model) to female university students, who are one of the groups that are vulnerable to being victimized in terms of cyber sexual violence.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
This research was conducted with a pre-test-post-test control group trial model to measure the effect of web-based cyber sexual violence training and counseling based on the information-motivation-behavioral skills (IMB) model given to young people on cyber sexual violence experience, sensitivity and cyber security ensuring behavior.
It was planned as a study.
The sample of our research will consist of female students from the Department of Primary Education and Kindergarten Teaching at Harran University.
The sample size of the study was calculated with Z test logistic regression using the G*Power 3.1.9.2 program, taking the gender risk of sexual cyberbullying as a reference in Klein and Cooper's study.
According to the power analysis, it was calculated that the sample of the research should have at least 85 people in the groups with an effect size of 0.20 and a 95% confidence interval determined by a 5% error level, with a 995% representative power of the universe.
It was planned to include an equal number of students from the first, second, third and fourth grades of the Primary School Teaching and Kindergarten Teaching departments in the research using the stratified sampling method.
Considering the losses from each group, it was planned to select a total of 200 people from the experimental (100 female classroom teaching students) and control group (100 female kindergarten teaching students).
Criteria for inclusion in the research; not being medically diagnosed with a psychological disease, being between the ages of 18-26, being single, being a classroom or kindergarten teacher student, using a smartphone, and having the opportunity to access the internet on a daily basis; Exclusion criteria were determined as failure to complete the intervention and failure to fill out the data collection form.
Research data will be obtained using the Participant Introduction Form, the Sensitivity Scale on Cyberbullying (SZSS) Young Adult Form, and the Personal Cybersecurity Ensuring Scale.
Data will be collected via online interview method on the web.
After the forms are applied to the experimental and control groups, the experimental group will be given a username and password to access the established website and they will receive the prepared training in video and word format.
It will be checked whether the students in the experimental group have watched the educational videos, reminder messages will be sent and calls will be made to them to watch all uploaded educational videos.
After training and counseling, the same tests will be applied again to the experimental group.
For the control group, only pre-test and post-test will be administered without any intervention.
Descriptive statistics such as percentage, arithmetic mean (X) and standard deviation (SD) were used to examine the socio-demographic characteristics of the students.
Chi-square test, paired sample t-test, independent samples t-test were used to determine whether there was a difference between the control variables and the experimental and control groups.
-test, Bonferroni test will be used to determine which group the difference between the groups originates from, independent samples t-test will be used to determine whether there is a difference between the mean scores of the scales in the experimental and control groups, and paired sample t-test will be used to compare the mean scores of the pre-test and post-test.
With the results obtained from this study, the effect of web-based cyber sexual violence training and counseling given to university students on cyber sexual violence victimization, sensitivity to cyber bullying and ensuring cyber security will be determined.
In the literature review, no studies were found on web-based training and consultancy against cyber sexual violence.
As a result of the data obtained from this study, it is thought that the cyber sensitivity and security of the web-based training and consultancy to be given to university students against cyber sexual violence can be determined and valuable data can be provided for the use of relevant professionals.
Study Type
Interventional
Enrollment (Estimated)
200
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Not being medically diagnosed with a psychological disease
- Being between the ages of 18-26
- Being single
- Being a classroom and kindergarten teaching student
- Using a smartphone
- Having the opportunity to access the internet on a daily basis
Exclusion Criteria:
- Inability to complete the intervention
- Not filling out the data collection form
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Classroom Teaching University Students Intervention Group
A special username and password will be given to the intervention group, which is randomly assigned to the female students of the classroom teaching department, to log in to the website, and they will be given a special access to the website.
Afterwards, training on cyber sexual violence will be given within the scope of the literature.
The scales will be applied to the students again after 12 weeks in order to see the effect of the behavior.
|
Web-based cyber sexual violence training and counseling will be provided to female classroom teaching students, who are the intervention group, and the effect of the intervention on cyber sexual violence experience, sensitivity and cyber security will be examined.
|
|
No Intervention: Kindergarten Teaching University Students Control Group
Participant Introduction Form, Cyber Sexual Violence Scale, Sensitivity Scale for Cyber Bullying (SZBÖ) Young Adult Form, Ensuring Personal Cyber Security Scale will be applied to the control group of kindergarten teaching female students as a pre-test.
The Participant Introduction Form, Cyber Sexual Violence Scale, Sensitivity Scale for Cyber Bullying (SZSS) Young Adult Form, and Ensuring Personal Cyber Security Scale will be applied to the control group again after an average of 8-10 weeks without any intervention.
In accordance with ethical principles, after the final results of the control group are collected, the videos in the training content will be sent to the control group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cyber Sexual Violence Scale
Time Frame: 6 months
|
The scale assessing sexual violence experienced online consists of 18 items.
The scale is a five-point Likert type (always = 5, often = 4, sometimes = 3, rarely = 2, never = 1).
The lowest score that can be obtained from the scale is 18 and the highest score is 90.
The scale consists of two subscales: "Unwanted sexual texts" and "Unwanted sexual desire".
In the Turkish validity and reliability study of the scale, Cronbach Alpha value was found to be 0.94 for the total score of the scale, 0.94 for the Sexual texts sub-dimension and 0.90 for the Unwanted sexual desire sub-dimension.
|
6 months
|
|
Sensitivity Scale on Cyberbullying Young Adult Form
Time Frame: 6 months
|
The scale is scored on a three-point scale as No (1), Sometimes (2), Yes (3).
The scale is one-dimensional and gives scores between 7 and 21.
A high score indicates high sensitivity.
Since the scale has not been normed, there is no cut-off score.
Cronbach's alpha coefficients were calculated for both versions to see how reducing the number of scales affected the internal consistency of the scale.
"While the alpha value for the 13-item version was .87, the value for the seven-item version was 0.83, and it was found that there was a minimal decrease in internal consistency after reducing it to six items."
|
6 months
|
|
Ensuring Personal Cyber Security Scale
Time Frame: 6 months
|
The scale consists of 5 factors and 25 items.
These factors are named as "protecting personal privacy" (10 items), "avoiding the untrustworthy" (4 items), "taking precautions" (5 items), "protecting payment information" (2 items) and "leaving no trace" (4 items). .
The Cronbach Alpha reliability coefficient of the 5-point Likert type scale was calculated as 0.735.
The reliability coefficients for the sub-dimensions are "protecting personal privacy" 0.763, "avoiding the untrustworthy" 0.771, "taking precautions" 0.704, "protecting payment information" 0.829 and "leaving no trace" 0.557.
The scale is suitable for individuals aged 18 and over.
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
June 1, 2024
Primary Completion (Estimated)
December 31, 2024
Study Completion (Estimated)
March 31, 2025
Study Registration Dates
First Submitted
May 7, 2024
First Submitted That Met QC Criteria
May 7, 2024
First Posted (Actual)
May 10, 2024
Study Record Updates
Last Update Posted (Actual)
May 10, 2024
Last Update Submitted That Met QC Criteria
May 7, 2024
Last Verified
May 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IU-SBE-ST-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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