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Emotional Management in Adolescents

A

Ankara Medipol University

Status

Completed

Conditions

Examining the Emotion Regulation Effectiveness to be Given to Adolescents
Emotional Regulation

Treatments

Behavioral: Group that will receive emotional regulation training

Study type

Interventional

Funder types

Other

Identifiers

NCT06849310
E-14588481-605.99-101274183

Details and patient eligibility

About

This study aims to give information about the content of the school-based emotion regulation program study designed for adolescent children to develop their emotion regulation skills. The study is a randomized controlled trial with adolescents aged 14-16 years (9th and 10th grade). Two high schools were selected for the research in Ankara, Türkiye. A face-to-face formal training consisting of four modules of four weeks (50 min/week). Based on the Vibrational Energy Theory, the program will be applied to the intervention group to be selected by the randomization method. The training topics include recognizing and accepting emotions, directed thinking and process orientation, and acceptance and willingness (reinforcement module) modules. With this intervention, adolescents' emotion regulation skills and psychological well-being are expected to increase, and anxiety levels will decrease. The program to be implemented will contribute to the acquiring and developing emotion regulation skills that deal with processes such as awareness, control, management, and acceptance of emotions in adolescents.

Key Words: adolescence, emotion, regulation, school

Enrollment

80 patients

Sex

All

Ages

14 to 16 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • . Criteria for inclusion in the research;

    • continuing their education in the 9th-10th grade,
    • agreeing to participate in the study,
    • giving written consent to participate in the study by their parents,
    • stating that they can participate in the four-week program,
    • speaking Turkish.

Exclusion criteria

  • The criteria for exclusion from the study were:

    • the student has a medically diagnosed mental problem that will prevent the student from following the program,
    • the student has a psychological medical diagnosis, and
    • he/she is receiving psychiatric medication or therapy.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

80 participants in 2 patient groups

Participants who will receive emotion regulation training.
Experimental group
Description:
This study was planned as a randomized controlled trial. The 9th and 10th grades of two high schools with the same status in the capital of Türkiye will constitute the sample of the research.Adolescents will be randomized as an intervention and control group after stratification according to the mean score of the scale, gender (girls/boys), and grades (9th and 10th grades). Letters will be given to the intervention and control groups. According to the coin toss method, the letter A will be given to the initiative group and the letter B will be given to the control group. Randomization will be performed by a statistician independent of the research using the www.randomizer.org site. Adolescents will not be informed that they will be an intervention or control group. Criteria for inclusion in the research; (a) continuing their education in the 9th-10th grade, (b) agreeing to participate in the study, (c) giving written consent to participate in the study by their parents, (d) stating t
Treatment:
Behavioral: Group that will receive emotional regulation training
Participants who will receive no intervention
No Intervention group
Description:
All forms will be administered to adolescents in the control group twice, before and after the program (except for the descriptive characteristic data form). After the study is completed, the control group will be given the same training and written material.

Trial contacts and locations

1

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Central trial contact

Merve Oral, Lecturer

Data sourced from clinicaltrials.gov

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