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

Sponsor
Tel-Aviv Sourasky Medical Center (Other)
Overall Status
Unknown status
CT.gov ID
NCT01321528
Collaborator
(none)
35
1
9
3.9

Study Details

Study Description

Brief Summary

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 or Disease Intervention/Treatment Phase

    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.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    35 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Official Title:
    Pilot Clinical Trial of Inquiry-based Stress Reduction (IBSR) Program for Health Care Professionals
    Study Start Date :
    Mar 1, 2011
    Anticipated Primary Completion Date :
    Dec 1, 2011
    Anticipated Study Completion Date :
    Dec 1, 2011

    Arms and Interventions

    Arm Intervention/Treatment
    IBSR Intervention group

    30 nurses in the geriatric departments in TASMC

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      18 Years to 67 Years
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      Yes
      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

      Locations

      Site City State Country Postal Code
      1 Tel-Aviv Sourasky Medical Center Tel-Aviv Israel 64239

      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

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT01321528
      Other Study ID Numbers:
      • TASMC 11 YL 0037 CTIL
      First Posted:
      Mar 23, 2011
      Last Update Posted:
      Mar 28, 2011
      Last Verified:
      Mar 1, 2011
      Additional relevant MeSH terms:

      Study Results

      No Results Posted as of Mar 28, 2011