Motivational Interviewing-Based Training

May 16, 2025 updated by: Kamile çiftci, Muş Alparslan University

The Effect of Motivational Interviewing-Based Training on Peer Bullying, Social Exclusion and Aggression in Secondary School Students

The middle school period is the period when children begin to experience physical, emotional and social development and try to adapt to psychological changes. In this age group, which is seen as a transition period, the child's academic success and acceptance by peers and friends are also important. The problems experienced during this period can continue in adulthood and children are more likely to experience loneliness, sleep disorders, depression, anxiety, eating disorders, low self-esteem, suicidal thoughts, absenteeism and a decrease in academic success. For this reason, early detection of risky behaviors that threaten children's health and evaluation of health promotion practices are very important issues for child health nursing.

In recent years, peer bullying, aggression and social exclusion have increased and continue to increase in the middle school period, also called early adolescence. For this purpose, a study was needed to identify the situation in middle school students and reduce this negativity. In this respect, it is thought that the study will contribute to the literature. In addition, if the hypotheses of the study are confirmed, it is expected that similar training will be provided in other schools and contribute to the reduction of risky behaviors.

The aim of this study is to determine the effects of motivational interviewing-based education on peer bullying, social exclusion and aggression in secondary school students and to offer suggestions for situations where deficiencies are observed based on the findings obtained.

Study Overview

Status

Not yet recruiting

Detailed Description

The universe of the study consists of 1 secondary school selected by simple random method from 39 secondary schools located in the city center affiliated to the Muş Provincial Directorate of National Education. G Power 3.1.9.7 program was used to determine the sample size for the study. The program used the ''A priori: compute required sample'' analysis method. Accordingly, when the first type error amount (α = 0.05) was taken at an effect size of 0.365 (Seyhan Şahin & Ayaz-Alkaya, 2024), it was determined that the number of people to be included in the study to reach 99% power was 60 (30 intervention, 30 control).

Experimental and control groups will be determined by simple random method among the students who accept to participate in the research. Pre-test will be applied to the students in the control group, post-test will be applied 6 weeks after the pre-test and control test will be applied 3 months after the post-test. 6-week motivational interview based training will be given to the students in the experimental group after the pre-test. Post-test will be applied at the end of the training and control test will be applied 3 months after the post-test. In the study, first the control group and then the experimental group will be included in the study..

Study Type

Interventional

Enrollment (Estimated)

80

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 Contact

Study Locations

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

  • Child

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Being 12-13 years old
  • Being in one of the 6th and 7th grades of middle school
  • Having a high score on the ''Peer Bullying Determination Scale''
  • Being willing to participate in the research
  • Not having a communication barrier
  • The student and their parents having signed the informed consent form.

Exclusion Criteria:

  • Having a low score on the ''Peer Bullying Determination Scale''
  • The volunteer not wanting to continue during the research
  • Encountering any communication barriers during the research
  • Answering the data collection forms incompletely or incorrectly

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental group
After the pre-test, motivational interview-based training consisting of six sessions will be applied to the students in the experimental group, once a week. A pre-test, post-test (after 6 weeks) and a control test will be applied to both groups. At the end of the training, the training materials will be shared with the students.
After the pre-test, motivational interviewing-based training consisting of six sessions, once a week, will be applied to the students in the experimental group. A pre-test, post-test (after 6 weeks) and control test will be applied to both groups. At the end of the training, training materials will be shared with the students.
No Intervention: Control group
The researcher will not apply any intervention to the control group other than the individual coping methods they apply in their daily lives. The training materials will be shared with the control group students at the end of the training.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
EFFECTS OF MOTIVATIONAL INTERVIEWING-BASED EDUCATION GIVEN TO SECONDARY SCHOOL STUDENTS ON PEER BULLYING, SOCIAL EXCLUSION AND AGGRESSION
Time Frame: First, a pre-test will be applied to students in both the experimental and control groups. A post-test will be applied to students in the control group after 6 weeks and a control test will be applied 3 months after the post-test. No intervention will be
In the study, motivational interview-based training will be applied as a nursing intervention. After receiving institutional permission, a pre-test will be applied to students who agree to participate in the study to determine peer bullying. Students whose total scale score is above the average level will be randomly selected and included in the study will be determined. The study will begin after both groups have signed an informed consent form (both students and parents). In collecting research data, the "Introductory Information Form", "Peer Bullying Determination Scale", "Social Exclusion Scale for Children (SESC)", and "Aggression Scale" will be used.
First, a pre-test will be applied to students in both the experimental and control groups. A post-test will be applied to students in the control group after 6 weeks and a control test will be applied 3 months after the post-test. No intervention will be

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Kamile ÇİFTCİ, Muş Alparslan University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

September 1, 2025

Primary Completion (Estimated)

March 1, 2026

Study Completion (Estimated)

June 15, 2026

Study Registration Dates

First Submitted

March 24, 2025

First Submitted That Met QC Criteria

May 7, 2025

First Posted (Actual)

May 14, 2025

Study Record Updates

Last Update Posted (Actual)

May 21, 2025

Last Update Submitted That Met QC Criteria

May 16, 2025

Last Verified

May 1, 2025

More Information

Terms related to this study

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

product manufactured in and exported from the U.S.

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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