Mindfulness Based Resilience Training (MBRT)
Primary Purpose
Stress, Psychological
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
MBRT ClassRoom and Phone Application
Phone application only
Questionnaires
Sponsored by
About this trial
This is an interventional health services research trial for Stress, Psychological focused on measuring well-being, stress, resilience, self-compassion
Eligibility Criteria
Inclusion:
- Stress subscale of the DASS-21 needs to be a score 5 or greater and
- Must have a smart Phone, and
- Ability to attend at least 5 complete sessions.
Exclusion :
- Stress subscale of the DASS-21 less than 5.
- Must have a smart Phone.
Sites / Locations
- Mayo Clinic in Arizona
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
MBRT ClassRoom and Phone Application
Phone application only
Questionnaires
Arm Description
MBRT ClassRoom and Phone Application
Phone application only
Questionnaires
Outcomes
Primary Outcome Measures
Changes in scores using the DASS-21(Depression Anxiety and Stress Scales) questionnaire
Secondary Outcome Measures
Full Information
NCT ID
NCT02419430
First Posted
April 14, 2015
Last Updated
May 14, 2016
Sponsor
Mayo Clinic
Collaborators
Arizona State University
1. Study Identification
Unique Protocol Identification Number
NCT02419430
Brief Title
Mindfulness Based Resilience Training
Acronym
MBRT
Official Title
Mindfulness Based Resilience Training for Employees at Mayo Clinic
Study Type
Interventional
2. Study Status
Record Verification Date
May 2016
Overall Recruitment Status
Completed
Study Start Date
April 2015 (undefined)
Primary Completion Date
March 2016 (Actual)
Study Completion Date
March 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mayo Clinic
Collaborators
Arizona State University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The investigators aim to evaluate the Mindfulness Based Resilience Training (MBRT) intervention for Mayo Clinic employees in order to provide evidence for improved ability to cope with stress and decreased work-related burnout and stress-related symptoms as a result of MBRT training. In addition, the investigators aim to compare the effects of MBRT + smartphone sleep feedback, a smartphone resilience intervention + smartphone sleep feedback, or waitlist control +smartphone sleep feedback in a randomized clinical trial in a sample of 75 Mayo Clinic employees.
Detailed Description
The investigators aim to compare the effects of MBRT + smartphone sleep feedback, a smartphone resilience intervention + smartphone sleep feedback, or waitlist control +smartphone sleep feedback in a randomized clinical trial in a sample of 75 Mayo Clinic employees. Specific self-report outcomes include: well-being, stress, anxiety, depression, fatigue, resilience, self-compassion, and burn-out, assessed at pre-, post- and 3-month followup. Objective outcomes, derived from smartphone-driven self-monitoring, include sleep quality and emotional experiencing, assessed throughout the six-week intervention period. The investigators will explore whether changes in objectively measured sleep quality and emotional experiencing will mediate treatment effects on self-report outcomes. The investigators will also explore whether treatment effects are more robust in self-selected versus randomized groups by drawing on the investigators' existing data.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stress, Psychological
Keywords
well-being, stress, resilience, self-compassion
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
MBRT ClassRoom and Phone Application
Arm Type
Active Comparator
Arm Description
MBRT ClassRoom and Phone Application
Arm Title
Phone application only
Arm Type
Active Comparator
Arm Description
Phone application only
Arm Title
Questionnaires
Arm Type
Active Comparator
Arm Description
Questionnaires
Intervention Type
Behavioral
Intervention Name(s)
MBRT ClassRoom and Phone Application
Intervention Description
2 hours/week for 6 week, in classroom intervention involving mindfulness based resilience training.focused on mindfulness and self-compassion training, including body awareness, breath awareness, mindful movement, awareness of thoughts, and awareness of emotion. Core concepts included: normalizing experience of stress and changing one's relationship with an experience; learning to be a compassionate observer of self in order to appreciate the moment; recognizing undue efforts to control something that has already happened; shifting attention to felt body sense and away from the narrative; and redirecting attention to a value as a way of evoking positive states that enhance the present moment experience. Participants also use the smartphone to track their sleep and subjective well-being.
Intervention Type
Behavioral
Intervention Name(s)
Phone application only
Intervention Description
Participants will track their sleep and subjective well-being and also choose one of the following weekly challenges, which is completed via smartphone interactions:
Joys of Life
Count your blessings
Think differenc, feel better
Exercising --> Happier
+ Exercising --> Sleep
Pre-Sleep routine
Eat that frog
Mindful Meditation
Intervention Type
Behavioral
Intervention Name(s)
Questionnaires
Intervention Description
At baseline, immediately after the last MBRT session (6 weeks) and again at 3 and 6 months, all participants will complete questionnaires, including: 1) WHO-5 Well-Being Index; 2) DASS-21; 3) VAS-Fatigue; 4) MBI-Human Services version; 5) Self-Compassion Scale; 6) Connor-Davidson 2-item resilience scale; 7) Compassion to others scale.
Primary Outcome Measure Information:
Title
Changes in scores using the DASS-21(Depression Anxiety and Stress Scales) questionnaire
Time Frame
Baseline to 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion:
Stress subscale of the DASS-21 needs to be a score 5 or greater and
Must have a smart Phone, and
Ability to attend at least 5 complete sessions.
Exclusion :
Stress subscale of the DASS-21 less than 5.
Must have a smart Phone.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cynthia Stonnington, MD
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic in Arizona
City
Scottsdale
State/Province
Arizona
ZIP/Postal Code
85259
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Mindfulness Based Resilience Training
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