IBSR Meditation Technique for Teachers' Burnout
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|ClinicalTrials.gov Identifier: NCT02455947|
Recruitment Status : Completed
First Posted : May 28, 2015
Last Update Posted : May 28, 2015
|Condition or disease||Intervention/treatment|
|Burnout, Professional||Other: Inquiry Based Stress Reduction (IBSR)|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||60 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Supportive Care|
|Official Title:||The Effect of Inquiry Based Stress Reduction (IBSR) Meditation Technique on Levels of Burnout and Wellbeing Among Teachers.|
|Study Start Date :||September 2013|
|Primary Completion Date :||August 2014|
|Study Completion Date :||February 2015|
Experimental: Inquiry Based Stress Reduction (IBSR)
IBSR intervention is the clinical implementation of a mindful-process, named "The Work" developed by Byron Katie.It teaches the individual to identify and question the thoughts that causes stress and suffering through four questions and turnarounds.
Other: Inquiry Based Stress Reduction (IBSR)
During a 12-week intervention program, participants will be encouraged to identify and inquire their stressful thoughts.All the sessions were standardized according to a training manual, and were assessed after each session for maintaining consistency in the program.
Other Name: The Work
No Intervention: Control group
A non interventional group/ The participants completed questionnaires before and after the intervention.
- Burnout levels, Maslach Burnout Inventory (MBI) [ Time Frame: 3 months ]emotional exhaustion and personal accomplishment
- Positive and Negative Affect Scale (PANAS) [ Time Frame: 3 months ]Positive and Negative emotions at daily life
- Depression, Anxiety, Stress (DASS) [ Time Frame: 3 months ]Clinical psycological symptoms
- Perceived Stress Scale (PSS ) [ Time Frame: 3 months ]Stress levels at daily life
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02455947
|Principal Investigator:||Shahar Lev-Ari, PhD||Integartive Medicine, Tel Aviv Medical Center|