Trial of Inquiry-based Stress Reduction (IBSR) Program for Health Care Professionals

The recruitment status of this study is unknown because the information has not been verified recently.
Verified March 2011 by Tel-Aviv Sourasky Medical Center.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Tel-Aviv Sourasky Medical Center
ClinicalTrials.gov Identifier:
NCT01321528
First received: March 10, 2011
Last updated: March 24, 2011
Last verified: March 2011
  Purpose

The IBSR (Inquiry-based stress reduction) intervention, developed by Byron Katie (www.thework.com), trains subjects to reduce their perceived level of stress by self-inquiry of their thoughts and beliefs connected to stressful circumstances or symptoms. This meditative process, named "The Work", enables the participants to identify and question the stressful thoughts that cause their suffering. The core of IBSR is simply four questions and a turnaround, which is a way of experiencing the opposite of what the participant believes. This process is simple, powerful and can be easily implemented in daily life.

Therefore, on the basis of previous data and beneficial observations the investigators postulate that the clinical utility of IBSR mediation program may alleviate stress and rate of burnout and improve quality of life among health care professionals. Thus, we will conduct a pilot/feasibility Observational study designed to:

  • Assess feasibility of a IBSR intervention by examining attendance, drop-out rates, and program satisfaction.
  • investigate whether IBSR intervention is efficacious in alleviating stress and rate of burnout and improving quality of life among health care professionals.

Condition
Behavioral Symptoms

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Prospective
Official Title: Pilot Clinical Trial of Inquiry-based Stress Reduction (IBSR) Program for Health Care Professionals

Further study details as provided by Tel-Aviv Sourasky Medical Center:

Estimated Enrollment: 35
Study Start Date: March 2011
Estimated Study Completion Date: December 2011
Estimated Primary Completion Date: December 2011 (Final data collection date for primary outcome measure)
Groups/Cohorts
IBSR Intervention group
30 nurses in the geriatric departments in TASMC

Detailed Description:

Study Goals To investigate whether IBSR intervention is efficacious in alleviating stress and rate of burnout and improving quality of life among health care professionals.

Study methodology The proposed study is pilot/feasibility intervention study with pre and post measures. 30 participants will receive Inquiry-based stress reduction (IBSR) group intervention.

Population The pilot intervention group will consist 30 nurses at the Geriatric Rehabilitation Department in the Tel Aviv Sourasky Medical Center (TASMC) who are willing to participate in this study.

Data collection procedures

  1. Assessments will be taken at an initial baseline orientation and at the end of the 12-week intervention.
  2. One week before IBSR classes will start, a baseline orientation will be held at this session, informed consent will be obtained, baseline data will be collected, and a brief overview of the IBSR program will be provided, which will highlight the 12-week class schedule.

Intervention

  1. Subjects will receive weekly 3.5 hour sessions conducted by two facilitators trained in IBSR and certified by BKI to conduct this intervention.
  2. Class size will range from 12-16 participants.
  3. All the sessions will be standardized and follow the training manual developed to maintain consistency in the program.
  4. Subjects will receive a training manual and CD's to support home practice of various forms of inquiry practices.
  5. The training manual will include weekly exercises, and program content related to the content identified below. In addition, the manual will include a weekly diary for recording homework practice activities.

The IBSR-BC program is a 12-week program adapted for consideration of health professionals well-being. During the process, participants will be encouraged to identify and inquire about their stressful thoughts: regarding health and illness, relationships with others, Beliefs that prevent them to promote their health, self judgments, perception of death and suffering. This intervention provides for management of specific emotional/psychological symptoms (stress, anxiety, depression) and physical symptoms, such as fatigue and sleeps disorders and enables the participants to inquire and be relieved of their stressful thoughts, and emotions caused by these thoughts. Through the use of self-inquiry practices subjects are taught to increase awareness of their thoughts and feelings, to observe their emotional and physical responses during situations perceived by them as stressful, and allow their mind to return to its true, peaceful, creative nature. Through the process of self inquiry, subjects take an active role in investigating their stressful thoughts, and by this regulating their stress and managing symptoms and emotions, thus enabling them to cope better with with emotional stress and burnout.

Throughout the 12-week IBSR (HCP - health care professionals) program, all subjects will be requested to formally meditate and perform self inquiry exercises alone or with a partner for a minimum of 15 min per day.

  Eligibility

Ages Eligible for Study:   18 Years to 67 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

30 participants nurses in the geriatric departments in TASMC

Criteria

Inclusion Criteria:

  1. nurses in the geriatric departments in TASMC
  2. Willing to sign an informed consent
  3. Age 18-67

Exclusion Criteria:

nursing assistants employees

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01321528

Contacts
Contact: yaffa lerman, MD 972-3-6974074 yaffale@tasmc.health.gov.il
Contact: Shahar Lev-ari, PhD 972-3-6947506 shaharl@tasmc.health.gov.il

Locations
Israel
Tel-Aviv Sourasky Medical Center Recruiting
Tel-Aviv, Israel, 64239
Contact: yaffa lerman, MD    972-3-6974074    yaffale@tasmc.health.gov.il   
Contact: shahar Lev-ari, PhD    972-3-6947506    shaharl@tasmc.health.gov.il   
Sponsors and Collaborators
Tel-Aviv Sourasky Medical Center
Investigators
Principal Investigator: Yaffa Lerman, MD Tel Aviv Sourasky Medical canter
Study Director: Shahar Lev Ari, PHD Tel-Aviv Sourasky Medical Center
  More Information

No publications provided

Responsible Party: Yaffa Lerman MD, Tel Aviv Sourasky Medical Center
ClinicalTrials.gov Identifier: NCT01321528     History of Changes
Other Study ID Numbers: TASMC 11 YL 0037 CTIL
Study First Received: March 10, 2011
Last Updated: March 24, 2011
Health Authority: Israel: Ethics Commission

Additional relevant MeSH terms:
Behavioral Symptoms

ClinicalTrials.gov processed this record on October 23, 2014