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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01605604
Other study ID # si496-2010
Secondary ID
Status Completed
Phase N/A
First received April 25, 2012
Last updated July 26, 2012
Start date October 2011
Est. completion date July 2012

Study information

Verified date July 2012
Source Mahidol University
Contact n/a
Is FDA regulated No
Health authority Thailand: Ethical Committee
Study type Interventional

Clinical Trial Summary

The pupose of the study is to determine the effectiveness of the Buddhist integrated group intervention improve the mindfulness in adolescents by a randomized controlled trial.The study divede the adolescents in two groups group A recieved the 8 time Buddhist group interventions.Group recieved nothing.The measurement were done pre and post intervention at week1 and week8.The mindfulness score ,the EQ,the MASS score were compared between both groups.


Description:

Adolescence behavioural problems are increasing including learning disabilities,game addiction,intolerance etc.The improvement of mindfulness ,the emotional quotient(EQ) proved to be effective to reduce the problems.The original teaching methods in school or in the temple are inadequate from increasing number of adolescent problems. The new technique integrated between Buddhism and group intervention is proposed to improve the mindfulness and EQ in adolescence.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date July 2012
Est. primary completion date March 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 10 Years to 15 Years
Eligibility Inclusion Criteria:

- adolescents

Exclusion Criteria:

- incomplete qeustionaire and intervention

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Other Conditions That May Be A Focus of Clinical Attention

Intervention

Behavioral:
buddhist mind fullness
there are two group one group recieve Buddhist mindfulness group intervention 8 times second group recieve nothing

Locations

Country Name City State
Thailand Faculty of Medicine Siriraj Hospital Mahidol University Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Mahidol University

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary The mindfulness score,The EQ score,the MASS score of the participants after intervention. 1 year Yes
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