- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05118880
Evaluation Of The Effectiveness Of The Peer Bullying Consultancy Program Based On The Interpersonal Relations Model
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Ankara, Turkey
- Kadriye Demir
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
The criteria for inclusion in the study are as follows.
- Being 11 or 12 years old,
- Having an internet connection at home,
- Having a computer and/or phone for internet access,
- Having at least one standard deviation above the school average in the PBIS-SSB sub-dimension score,
- The voluntary acceptance of the child and his/her parents to participate in the research
Exclusion Criteria:
• Having any physical or mental health problems,
. Having a diagnosis of chronic disease
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: control group
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Experimental: İntervention group
the children enrolled in the Peer Bullying Counseling Program based on the Interpersonal Relationship Model
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The content of the program was created by the researcher in line with the issues that peer bullying children need support based on their bullying-related characteristics in the light of the relevant literature.
Education topics prepared in this framework; 'Empathy', 'Peer Bullying', 'Anger Management' and 'Happy Friendship Relationships' were determined.
The main nursing problem of the research is "peer bullying".
The main purpose of the Peer Bullying Counseling Program is to improve the empathy skills of the bullying child, to enable them to gain the right perspective towards bullying, to develop anger control, and to help them establish happy friendships.
The content of the Peer Bullying Counseling Program; drawing, brainstorming, empathy demonstration, white paper activity, educational matching game, peer bullying demonstration, case studies, educational emotion puzzle game, anger control information video were applied using educational techniques.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Bullying Cognitions Scale for Children mean scores (BCSC)
Time Frame: Pre-test and post-test
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The BCSC was developed to assess the cognitive characteristics associated with peer bullying in children.
The twenty-two-item scale was graded in a 4-point likert type ('completely true', 'quite true', 'somewhat true', 'not true at all').
The 'completely correct' response was rated as 4 points, the 'quite correct' response as 3 points, the 'somewhat correct' response as 2 points, and the 'not at all correct' response as 1 point.
There is no reverse item in the scale.
The scale is evaluated with a total score.
The highest total score that can be obtained from the scale is "88" and the lowest score is "22".
The higher the scores, the higher the cognitions about bullying.
In other words, bullying is considered normal and normal.
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Pre-test and post-test
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Empathy Scale for Children and Adolescents (ESCA)
Time Frame: Pre-test and post-test
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The scale consists of 21 items.
The scale is filled by giving one of the two answers as 'Yes' or 'No' to its items.
The 'Yes' response was scored as 1 point, and the 'No' response as 0 points.
However, some items (2,8,9,14,15,16,17,19,20 and 21) in the scale are reverse scored.
In this case, 1 point was given to the "no" answer given to the item in question, and 0 point was given to the "yes" answer.
The lowest score that can be obtained from the scale is 0, and the highest score is 21.
As the score obtained from the scale increases, the empathic tendency increases, and as the score decreases, the empathic tendency decreases.
The internal consistency coefficient of the scale was found to be 0.84 by Gürtunca and Karakale.
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Pre-test and post-test
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Friendship Relations and Anger Control Evaluation Form (FRACEF)
Time Frame: Pre-test and post-test
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The Friendship Relations and Anger Control Evaluation Form was created considering the PBCP (Peer Bullying Counseling Program) content.
The form was prepared to measure the happiness levels of children in friendship relationships, sample behavior information about happy friendship relationships, and their knowledge and competence levels about anger control.
The Friendship Relations and Anger Control Evaluation Form consists of 5 questions, two for happy friendship relationships and three for anger control.
A total of 50 points can be obtained from the form, with 10 points for each question.
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Pre-test and post-test
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- LokmanHekimU-SBF-HB-KD-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
SPSS data will be shared during the publication of the article in accordance with the principle of protection of personal data.
Evaluation of Data:
Evaluation of the data was made in SPSS for Windows 11.5 (Chicago INC.) package program. Number, percentage, arithmetic mean, standard deviation, median, and minimum-maximum values were used in the intra-group distribution of descriptive data and scale scores. Non-parametric tests (Wilcoxon Test for intragroup difference, Man-Whitney U Test for intergroup difference) were used for statistical analysis of data that did not show normal distribution. The Kolmogorov-Smirnov test was used in the control group with an n≥30 score for the normal distribution of the scale mean scores. Statistical significance value was accepted as p<0.05.
It is aimed that this research will be published in the Journal of School Nursing.
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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