- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02455947
IBSR Meditation Technique for Teachers' Burnout
May 27, 2015 updated by: Dr. Shahar Lev- Ari, PhD, Tel Aviv Medical Center
The Effect of Inquiry Based Stress Reduction (IBSR) Meditation Technique on Levels of Burnout and Wellbeing Among Teachers.
The purpose of this study is to investigate the effect of Inquiry based stress reduction (IBSR) meditation technique on levels of burnout and wellbeing among teachers.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Teachers' burnout is a well-known phenomenon with personal and professional implications.
The current study investigates the effect of inquiry based stress reduction (IBSR) technique on burnout and well-being among teachers.
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
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
20 years to 62 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- All the teachers working in 'Begin' high-school, Rosh Hayin, Israel
- agreed to sign an informed consent form
Exclusion Criteria:
- Teachers with previous experience with IBSR technique
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: Supportive Care
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
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.
|
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 Names:
|
No Intervention: Control group
A non interventional group/ The participants completed questionnaires before and after the intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Burnout levels, Maslach Burnout Inventory (MBI)
Time Frame: 3 months
|
emotional exhaustion and personal accomplishment
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Positive and Negative Affect Scale (PANAS)
Time Frame: 3 months
|
Positive and Negative emotions at daily life
|
3 months
|
Depression, Anxiety, Stress (DASS)
Time Frame: 3 months
|
Clinical psycological symptoms
|
3 months
|
Perceived Stress Scale (PSS )
Time Frame: 3 months
|
Stress levels at daily life
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Shahar Lev-Ari, PhD, Integartive Medicine, Tel Aviv Medical Center
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
September 1, 2013
Primary Completion (Actual)
August 1, 2014
Study Completion (Actual)
February 1, 2015
Study Registration Dates
First Submitted
May 20, 2015
First Submitted That Met QC Criteria
May 27, 2015
First Posted (Estimate)
May 28, 2015
Study Record Updates
Last Update Posted (Estimate)
May 28, 2015
Last Update Submitted That Met QC Criteria
May 27, 2015
Last Verified
May 1, 2015
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- TelAvivMC
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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