- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06972030
- Original Trial
Motivational Interviewing-Based Training
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
Conditions
Intervention / Treatment
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
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Kamile ÇİFTCİ
- Phone Number: +905389454274
- Email: k.ciftci@alparslan.edu.tr
Study Locations
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MUŞ, Turkey, 49250
- Muş Alparslan University
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Contact:
- Kamile ÇİFTCİ
- Phone Number: 05389454274
- Email: k.ciftci@alparslan.edu.tr
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
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
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.
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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.
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|
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.
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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
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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.
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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
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Kamile ÇİFTCİ, Muş Alparslan University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Estimated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- Peer Bullying
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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