Evaluation Of The Effectiveness Of The Peer Bullying Consultancy Program Based On The Interpersonal Relations Model

November 3, 2021 updated by: Kadriye Demir
The research was conducted in experimental design with intervention-control group and pretest-posttest in order to examine the effectiveness of the Peer Bullying Consultancy Program (PBCP), is based on the Interpersonal Relations Model (IPM), on 11-12 years old children who are bullying. The sample group of the study consisted of children (intervention group/n=29; control group/n=32) were attending 5th and 6th grades in two different randomized designated secondary schools after stratified sampling, had high Peer Bullying Determination Scale Bully Behavior. The PBCP was implemented to the children in the intervention group in 2 face-to-face and 5 online individual interviews in 26 days. To increase the peer bullying cognition level, to develop empathy skills, to improve friendship relations, to increase anger control of children who are bullying in intervention group, content suitable for age characteristics was developed within the scope of PBCP various training techniques (brainstorming, educational game, demonstration, case study, video watching) used. The data were collected using Sociodemographic Information Form, the Bullying Related Cognitions Scale for Children (BRCSC), the Empathy Scale for Children and Adolescents (ESCA), Friendship Relations and Anger Control Assessment Form. Data collection tools were applied to the children in the intervention group at the beginning and at the end of the PBCP, and to the children in the control group with an interval of 26 days. In the study, children in the intervention group had lower scores on the BRCSC; had higher scores on the ESCA, Self-Reporting Happiness Level in Friendship Relations, Sample Behavior Knowledge Level for Happy Friendship, Understanding Level of Anger Symtoms, Knowledge Level of Anger Control and Self-Reporting Anger Control Level than the children in the control group (p<0.05). It has been determined the PBCP based on the IRM is effective for children aged 11-12 who are bullying. It is recommended nurses develop model-based, individual counseling and training program in which different educational techniques are used in accordance with the age characteristics in order to support the growth, development of children who are bullying within the framework of their roles such as advocate, consultant, leader.

Study Overview

Study Type

Interventional

Enrollment (Actual)

61

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Ankara, Turkey
        • Kadriye Demir

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

11 years to 12 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

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

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: Supportive Care
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: control group
Experimental: İntervention group
the children enrolled in the Peer Bullying Counseling Program based on the Interpersonal Relationship Model
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Bullying Cognitions Scale for Children mean scores (BCSC)
Time Frame: Pre-test and post-test
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.
Pre-test and post-test
Empathy Scale for Children and Adolescents (ESCA)
Time Frame: Pre-test and post-test
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.
Pre-test and post-test

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Friendship Relations and Anger Control Evaluation Form (FRACEF)
Time Frame: Pre-test and post-test
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.
Pre-test and post-test

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 (Actual)

February 14, 2020

Primary Completion (Actual)

October 10, 2020

Study Completion (Actual)

January 24, 2021

Study Registration Dates

First Submitted

October 1, 2021

First Submitted That Met QC Criteria

November 3, 2021

First Posted (Actual)

November 12, 2021

Study Record Updates

Last Update Posted (Actual)

November 12, 2021

Last Update Submitted That Met QC Criteria

November 3, 2021

Last Verified

November 1, 2021

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)?

YES

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

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.

Clinical Trials on Peer Bullying Counseling Program based on the Interpersonal Relationship Model

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