Trial of Inquiry Based Stress Reduction (IBSR) Program for BRCA1/2 Mutation Carriers

Hereditary Breast and Ovarian Cancer Syndrome Clinical Trial

Official title:

Evaluating the Effectiveness of Inquiry Based Stress Reduction (IBSR) Intervention Versus Regular Care of no Treatment on Well-being, Optimism and Health Behavior of BRCA1/2 Carriers: A Randomized Controlled Trial, RCT.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03162276
• Other study ID #: SHEBA-17-3856-EF-CTIL
• Status: Recruiting
• Phase: Phase 3
• Start date: July 1, 2017
• Est. completion date: December 30, 2020

Study information

• Verified date: September 2018
• Source: Sheba Medical Center
• Contact: Eitan Friedman, Prof.
• Phone: 972-3-5303173
• Email: eitan.friedman[@]sheba.health.gov.il
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Breast cancer (BC) is a major health problem and the most prevalent cancer among women.In a substantial proportion of familial cases, germ-line mutations in either BRCA1/2 can be detected. The only proven modality for active risk reduction (rather than passive early detection), is prophylactic surgery - prophylactic mastectomy and oophorectomy. While the majority of Jewish mutation carriers elect to undergo prophylactic oophorectomy at about age 40 years, in Israel only a minority perform prophylactic mastectomy. Another ramification of being a mutation carrier is the emotional stress associated with that discovery.Genetic information has profound implications for mutation carriers. The IBSR (Inquiry-based stress reduction) intervention, developed by Byron Katie, trains participants 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 provides skills for self-inquiry and management of stressful thoughts that can be easily implemented in daily life [ ]. Therefore, on the basis of previous data and beneficial observations we postulate that the clinical utility of IBSR mediation program may improve psychological and physical symptoms and quality of life among asymptomatic (oncologically healthy) BRCA1/ BRCA2 mutation carriers. Thus, we will conduct a pilot randomized controlled trial to scientifically investigate the effect of this intervention effects on BRCA1/2 mutation carriers.

Description:

Primary goal: to evaluate the effectiveness of IBSR intervention on psychological well-being of BRCA carriers.

Secondary goals:

• To understand the IBSR action mechanism and to develop a theoretical model.

• To examine the correlation between psychological well-being and optimism and health behaviors among carriers.

• To evaluate and define core beliefs related to psychological well-being, optimism and expectations among carriers.

• To evaluate and define the health related behaviors among carriers.

Rationale for studies: The rationale of the research emerges from two aspects. One aspect is the effort to establish a new intervention program for women in order to help them deal with the daily implications of being a BRCA carrier. Up to date, only few interventions were carried out in Israel and worldwide, and had several methodological limitations.

The other aspect is the combination of quantitative and qualitative tools in order to analyze the psychological implications of a complicated medical state and to establish an intervention program in order to reduce their adverse impact. This combination can significantly contribute to the understanding of the investigated issue and the participants' experience. The current research is comprehensive and rigorous, and it is based on a randomized controlled study, which was carried out with 118 Israeli women.

Research plan and milestones:

Research Design: A randomized controlled study offering IBSR intervention for BRCA carriers.

Research sample: 118 asymptomatic BRCA1/2 carriers, being followed-up in the high-risk clinic at Sheba hospital and meet the inclusion criteria:

asymptomatic carriers of BRCA1/2 mutation, level of Hebrew, age group and psychiatric illness. Age: 25-55

Intervention group: 59 carriers who will participate in a 8-12 sessions (up to 48 hours) group workshop of IBSR.

Control group: 59 carriers who will not participate in the workshop. They will complete questionnaires on the same time points as the intervention group. Participants who completed all the questionnaires will receive an IBSR kit for home practice.

Research outcomes: psychological well-being, optimism, satisfaction with life, mental well-being, quality of sleep health behaviors and perceptions. In addition, the main themes from the qualitative interviews.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 118
• Est. completion date: December 30, 2020
• Est. primary completion date: October 1, 2020
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 25 Years to 55 Years

Eligibility

Inclusion Criteria:

• Women who are carriers of one of the predominant Jewish mutations in BRCA1/2 genes, age 25-55 years, with no current or past history of cancer (except BCC), who are willing to sign an informed consent, and present mental clarity by the ability to comprehend and fulfill all the questionnaires.

Exclusion Criteria:

• Diagnosed with breast or ovarian cancer or any other cancer, risk reduction mastectomy, severe psychiatric diagnosis (e.g. bipolar disorder).

Related Conditions & MeSH terms

• Hereditary Breast and Ovarian Cancer Syndrome

Intervention

Behavioral:
• Inquiry Based Stress Reduction (IBSR) program
The IBSR (Inquiry-based stress reduction) intervention, developed by Byron Katie, trains participants 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 provides skills for self-inquiry and management of stressful thoughts that can be easily implemented in daily life
• Control
At end of intervention, the control group will receive a brief intervention consisting of a home kit for practicing IBSR techniques.

Locations

Country	Name	City	State
Israel	Eitan Friedman	Tel Hashomer
Israel	Sheba Medical Center	Tel-aviv

Sponsors (1)

Lead Sponsor	Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

References & Publications (2)

Landau C, Lev-Ari S, Cohen-Mansfield J, Tillinger E, Geva R, Tarrasch R, Mitnik I, Friedman E. Randomized controlled trial of Inquiry-Based Stress Reduction (IBSR) technique for BRCA1/2 mutation carriers. Psychooncology. 2015 Jun;24(6):726-31. doi: 10.1002/pon.3703. Epub 2014 Oct 18. — View Citation

Landau C, Mitnik I, Cohen-Mensfild J, Tillinger E, Geva R, , Friedman E. Lev-Ari S. Inquiry-based stress reduction (IBSR) meditation technique for brCA1/2 mutation carriers—A qualitative study. European Journal of Integrative Medicine; Dec 2016; 8 (6): 958-964

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The Ryff scale- Psychological well-being	Questionnaire	A measure assessing change between 3 time points (before the intervention, after 5 months (at the end of the intervention) and 3 months later)
Secondary	Life Orientation Test-Revise- LOT-R	This questionnaire assesses the degree of optimism	A measure assessing change between 3 time points (before the intervention, after 5 months (at the end of the intervention) and 3 months later)
Secondary	Satisfaction with life scale - SWLS d	This questionnaire assesses the degree of Satisfaction with the life	A measure assessing change between 3 time points (before the intervention, after 5 months (at the end of the intervention) and 3 months later)
Secondary	Pittsburgh Sleep Quality Inventory Questionnaire- PSQI	This questionnaire assesses the quality of sleep	A measure assessing change between 3 time points (before the intervention, after 5 months (at the end of the intervention) and 3 months later)
Secondary	Positive and negative affect schedule PANAS	This questionnaire assesses the degree of positive and negative feelings	A measure assessing change between 3 time points (before the intervention, after 5 months (at the end of the intervention) and 3 months later)
Secondary	Self-assessed health SAH	This questionnaire assesses the personal perceived health	A measure assessing change between 3 time points (before the intervention, after 5 months (at the end of the intervention) and 3 months later)
Secondary	Euroqol quality of life scale EQ-5D	This questionnaire assesses the quality of life	A measure assessing change between 3 time points (before the intervention, after 5 months (at the end of the intervention) and 3 months later)
Secondary	Perceived social support from family PSS-FA	This questionnaire assesses the perceived family support	A measure assessing change between 3 time points (before the intervention, after 5 months (at the end of the intervention) and 3 months later)
Secondary	Mindfulness attention awareness scale MAAS	This questionnaire assesses the degree of mindfulness attention	A measure assessing change between 3 time points (before the intervention, after 5 months (at the end of the intervention) and 3 months later)
Secondary	General self- efficacy GSE	This questionnaire assesses the degree of self- efficacy	A measure assessing change between 3 time points (before the intervention, after 5 months (at the end of the intervention) and 3 months later)
Secondary	Demographic and behavioral data	This questionnaire asks about demographics data and health behavior	A measure assessing change between 3 time points (before the intervention, after 5 months (at the end of the intervention) and 3 months later)