Efficacy of Brief Mindfulness Based Self- Compassion Intervention for Management of Anger Among Adolescents

August 6, 2024 updated by: Fatima Noor

Efficacy of Brief Mindfulness Based Self-Compassion Intervention for Management of Anger Among Adolescents

This study investigates the effectiveness of a short self-compassion mental intervention in reducing aggression among adolescents. Although they display potential, current solutions are arduous and time-consuming. The study provides preliminary results on the effectiveness of this method in addressing the lack of information. The intervention's simplicity and precision have the potential to greatly influence the treatment of teenage violence. This could lead to the general acceptance and implementation of mindfulness-based self-compassion, making it accessible at a reasonable cost. The study's brevity and specificity hold promise for broader implementation. A significant gap exists in the literature concerning brief mindfulness-based self-compassion interventions tailored specifically to address adolescent aggression. Most existing studies have explored more extended interventions or general mindfulness programs, leaving a dearth of research on the effectiveness of concise, targeted interventions for adolescents dealing with aggression.

Study Overview

Status

Completed

Conditions

Detailed Description

The study's focus on a brief mindfulness-based self-compassion intervention stands out as a resource-efficient and practical approach to addressing aggression in adolescents. This concise intervention's potential effectiveness offers the promise of a more accessible and cost-effective approach to addressing adolescent aggression, which is critical in our resource-constrained world. The study determined that the brief intervention is efficacious, enabling its adaptation and implementation in educational institutions, juvenile justice programs, and community organizations that work with belligerent adolescents. Due to its versatility, the conclusions of the study can be directly applied to real-world issues. The salient feature of this method is in its explicit targeting of adolescent aggression. By prioritizing self-compassion and mindfulness, this program aids in the regulation of emotions and reduces aggression among young individuals. Effective interventions have the potential to improve the psychological well-being, emotional control, and interpersonal connections of adolescents who display aggressive behavior. This study has the potential to make mindfulness-based self-compassion practices more easily available to a greater number of adolescents. This might lead to the development of practical and cost-effective solutions that promote emotional well-being and decrease aggressiveness. These strategies would have long-lasting advantages.

Study Type

Interventional

Enrollment (Actual)

25

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

    • Punjab
      • Multan, Punjab, Pakistan
        • Muhammad Rizwan

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
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  1. Students' age range of 13 to 19 years
  2. symptoms of aggression.

Exclusion Criteria:

Students who are not willing to participate

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: Screening
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Therapist
The only one researcher, an experienced mindfulness practitioner and group therapist, leads groups of 10-15 students in weekly 90-minute sessions to deliver the program.
session includes mindfulness exercises like breath awareness and body scans, self-compassion practices like self-kindness meditations, and emotional regulation strategies such as cognitive reappraisal and response modulation. Discussions focus on applying mindfulness and self-compassion to manage difficult emotions, improve interpersonal interactions, and reduce aggression. Home practice assignments encourage students to integrate mindfulness and self-compassion into their daily lives. The program curriculum is based on existing evidence-based interventions, including mindfulness-based stress reduction for teens.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Psychological Wellbeing
Time Frame: 1 Month
after the intervention (mindfullness) students shows the significant improvement in their psychological wellbeing
1 Month

Collaborators and Investigators

This is where you will find people and organizations involved with this 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 (Actual)

February 10, 2024

Primary Completion (Actual)

June 1, 2024

Study Completion (Actual)

June 10, 2024

Study Registration Dates

First Submitted

July 20, 2024

First Submitted That Met QC Criteria

August 6, 2024

First Posted (Actual)

August 9, 2024

Study Record Updates

Last Update Posted (Actual)

August 9, 2024

Last Update Submitted That Met QC Criteria

August 6, 2024

Last Verified

July 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • FJWU/EC/2024/81

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The ethical committee of FJWU Rawalpindi approved the research topic in the first phase. The principals of the government and private schools in Rawalpindi granted permission for the data collection. Prior to the commencement of the study, we debriefed the participants about the research topic and its conduct modalities. Participants were approached by purposive sampling. We obtained informal consent from both the students and the parents.

3.7.2 Phase II In the second phase of the research, the participants were randomly assigned to the control and intervention groups by using software. The interventional group exposed participants to Urdu-adapted and translated mindfulness-based self-compassion training. However, the control group either maintained their usual routine or standard care, or received a non-specific intervention. After the successful completion of mindfulness-based self-compassion training, both groups were evaluated. Pre- and post-assessment results were assessed.

IPD Sharing Time Frame

Six Month

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • ANALYTIC_CODE
  • CSR

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.

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