Clinical Trials Logo

Clinical Trial 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.


Clinical Trial 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

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT01321528
Study type Observational
Source Tel-Aviv Sourasky Medical Center
Contact yaffa lerman, MD
Phone 972-3-6974074
Email yaffale@tasmc.health.gov.il
Status Recruiting
Phase N/A
Start date March 2011
Completion date December 2011

See also
  Status Clinical Trial Phase
Completed NCT01217541 - Collaboration Between Department of Old Age Psychiatry and Nursing Homes N/A
Completed NCT00365859 - Study of Aripiprazole in the Treatment of Serious Behavioral Problems in Children and Adolescents With Autistic Disorder (AD) Phase 3
Recruiting NCT03624348 - The Impact of 8 Weeks of a Digital Meditation Application on Work Stress N/A
Recruiting NCT03670446 - Pharmacists' Intervention in Patients Using Novel Oral Anticoagulants:A Study on Behavioral Patterns N/A
Completed NCT04091633 - School Health Implementation Network: Eastern Mediterranean N/A
Withdrawn NCT00375557 - Safety and Efficacy of Divalproex and Quetiapine in Elderly Alzheimer's Dementia Patients Phase 4
Completed NCT00479271 - Evaluating the Effectiveness of a Community Based Intervention for Persons With Dementia and Their Caregivers in a Developing Country N/A
Completed NCT04587583 - WeCareAdvisor: A Web-Based Tool to Improve Quality of Life for Military Veterans With Dementia and Their Caregivers Phase 1/Phase 2
Recruiting NCT05591820 - A Randomized Controlled Trial on Brief Behavioral Parent Training N/A
Completed NCT03464955 - VR Usage in Non-Invasive Surgical Sub-Specialty Procedures N/A
Recruiting NCT04066985 - Targeting Adolescent Depressive Symptoms Via Brief, Web-Based Interventions N/A
Completed NCT04096274 - Working to Implement and Sustain Digital Outcome Measures N/A
Completed NCT03376633 - The Impact of a School-Based, Trauma-Informed CBT Intervention for Young Women N/A
Recruiting NCT03506672 - Assessing the Effectiveness of an Approach for Vocal Behaviors in Older People Living in Nursing Homes N/A
Not yet recruiting NCT05612711 - Dronabinol for Agitation in Dementia Crossover Trial Phase 2
Completed NCT02069912 - Multifaceted Depression and Cardiovascular Program N/A
Active, not recruiting NCT05353049 - How to Bathe a Person With Dementia? A Bathing Intervention Based on Basale Stimulation® for People With Moderate to Severe Dementia N/A
Completed NCT05599100 - Virtual Training for Latino Caregivers to Manage Symptoms of Dementia N/A
Recruiting NCT05989646 - Brain Activity Among Children With Overactive Bladder and Daytime Urinary Incontinence and Healthy Children N/A
Completed NCT05384704 - A Single Group Study of Empower@Home-an Internet Cognitive Behavioral Therapy Intervention N/A