- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06544044
Efficacy of Brief Mindfulness Based Self- Compassion Intervention for Management of Anger Among Adolescents
Efficacy of Brief Mindfulness Based Self-Compassion Intervention for Management of Anger Among Adolescents
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab
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Multan, Punjab, Pakistan
- Muhammad Rizwan
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Students' age range of 13 to 19 years
- symptoms of aggression.
Exclusion Criteria:
Students who are not willing to participate
Study Plan
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.
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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.
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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
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- FJWU/EC/2024/81
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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
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
Studies a U.S. FDA-regulated device product
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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