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Effects of Transcendental Meditation on Physician Burnout and Depression

Primary Purpose

Burnout, Professional, Depression, Insomnia

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Transcendental Meditation technique
Sponsored by
Marie Loiselle
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Burnout, Professional focused on measuring academic physician burnout, physician burnout, Intervention to reduce physician burnout, physician depression, physician insomnia, physician stress, Transcendental Meditation, TM

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Have an MD degree
  • Be an academic attending physician at the Loyola Chicago School of Medicine or Edward Hines, Jr. VA Hospital
  • Commit to attend all required sessions for learning the Transcendental Meditation (TM)technique and monthly follow-ups
  • Agree to practice TM twice daily for 20 minutes for the 4-month study period
  • Agree to complete both pre-and post-testing (at 1-month and 4-months) including both the entry and exit interviews.

Exclusion Criteria: current suicidal ideation, previous instruction in the TM technique

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Sites / Locations

  • Loyola University Stritch School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Transcendental Meditation Group

Control Group

Arm Description

Participants assigned to this group each received the intervention of 5 initial class instructions in the Transcendental Meditation technique, followed by 6 additional classes over the 4-month study period. Group participants were expected to practice the technique for 20 minutes twice per day for 4-months.

Participants assigned to this group served as wait-list controls

Outcomes

Primary Outcome Measures

Maslach Burnout Inventory
measures burnout level

Secondary Outcome Measures

Beck Depression Inventory
measures depression level
Insomnia Severity Index
measures insomnia level
Perceived Stress Scale
measures level of perceived stress
Brief Resilience Inventory
measures resilience level

Full Information

First Posted
October 12, 2018
Last Updated
October 17, 2023
Sponsor
Marie Loiselle
Collaborators
Loyola University Chicago
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1. Study Identification

Unique Protocol Identification Number
NCT03714204
Brief Title
Effects of Transcendental Meditation on Physician Burnout and Depression
Official Title
Effects of Transcendental Meditation on Physician Burnout and Depression: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
August 1, 2015 (Actual)
Primary Completion Date
June 30, 2016 (Actual)
Study Completion Date
September 30, 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Marie Loiselle
Collaborators
Loyola University Chicago

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This research study will examine the effects of the Transcendental Meditation (TM) technique on academic physician burnout, depression, insomnia, perceived stress, and resilience through a mixed methods approach.
Detailed Description
Burnout is pervasive among physicians in academia, with costly ramifications for individuals and institutions ($100,000-900,000/faculty replacement). The purpose of this study is to assess, both quantitatively and qualitatively, the effects of the TM technique as an intervention in lowering burnout, depression, perceived stress, insomnia, and to increase resilience in academic physicians. Research Study Hypotheses Quantitative hypothesis #1: Regular practice of the TM technique by academic physicians for 4 months will reduce symptoms of burnout compared to academic physicians not practicing the TM technique Quantitative hypothesis #2: Regular practice of the TM technique by academic physicians for 4 months will reduce symptoms of perceived stress, insomnia, depression and increase resilience compared to academic physicians not practicing the TM technique. Qualitative research questions: What are the daily challenges faced by academic physicians and how do they view their ability to handle them? Does regular practice of the TM technique improve their perception of their quality of life with regards to the challenges they face? Sample Size Estimate There is an effect size of .6225 when using changed scores for treatment and control groups, and their respective standard deviations, from a recent study using the TM technique as the intervention and measuring burnout using the Maslach Burnout Inventory (Elder, 2014). Applying Cohen's power tables for p<.05 to this effect size the number of subjects per group needed is 12. Recruiting 20 subjects per group will allow for 20% attrition. Study Design Overview The research design is a mixed methods randomized controlled trial (RCT) involving both a treatment and wait-list control group. Quantitative testing will be done three times: pretest followed by posttests at one and four months. The one month posttest is to assess any short term changes as well as a precaution against possible dropouts of either group before the four-month posttest. All subjects will be required to sign an informed consent form prior to participation. Qualitative data will be gathered through two individual 30-minute semi-structured interviews: the first (entry) before randomization, at the time of the quantitative pretest; and the second (exit) at the 4-month posttest. The independent variable is instruction in the TM technique, which includes introductory and follow-up sessions to be taught to the treatment group following their pretest and entry interview. Quantitative data will be analyzed using repeated measures analysis of variance. Qualitative data will be analyzed using a phenomenological approach of identifying main themes and sub themes from the pre and post intervention interviews. The interviews will be the only source of qualitative data. Separate analysis and discussions of quantitative and qualitative data will be merged together to examine their convergence and divergence. The Institutional Review Board at Maharishi University of Management approved the study in March 2015 followed by the Institutional Review Board at Loyola University Chicago approval in July 2015. The goal of this study is to see if the intervention alters quantitative measurements of burnout and to understand what kinds of challenges academic physicians face in their daily lives, how they view their ability to handle them, and whether either is transformed during the study period. Although much research has shown symptoms of burnout are largely present among physicians, and a few studies showed promising antidotes, none to date have made use of both quantitative and qualitative data in exploring an intervention for lowering burnout in academic physicians. This study will employ the advanced convergent mixed methods design which entails collecting both quantitative and qualitative data at pre-and posttest intervals, while adding the advanced feature of an intervention following pretesting. Study Protocol The researcher will oversee all test administration and tracking of subject compliance. All study related paperwork and online tests will be managed under appropriate institutional protocol for anonymity and confidentiality. Data will be securely stored appropriately on-line and the hard copies of the consent form kept under lock in the Vice-Dean of Education's office. To further protect the identity of reporting physicians, the identity of the medical school is, and will be, masked in this dissertation and further papers based on this dissertation. Adverse event reporting: If an adverse event is reported through testing or interviews (and it is a recent issue) it will be reported to the Principal Investigator who will speak to this potential study participant and recommend that they be seen in Employee Health. If the adverse event was suicidal ideation they would be excluded from the study until such time the event was resolved.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Burnout, Professional, Depression, Insomnia, Perceived Stress, Resilience
Keywords
academic physician burnout, physician burnout, Intervention to reduce physician burnout, physician depression, physician insomnia, physician stress, Transcendental Meditation, TM

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled trial
Masking
None (Open Label)
Masking Description
The names of individual participants
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Transcendental Meditation Group
Arm Type
Experimental
Arm Description
Participants assigned to this group each received the intervention of 5 initial class instructions in the Transcendental Meditation technique, followed by 6 additional classes over the 4-month study period. Group participants were expected to practice the technique for 20 minutes twice per day for 4-months.
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Participants assigned to this group served as wait-list controls
Intervention Type
Behavioral
Intervention Name(s)
Transcendental Meditation technique
Intervention Description
The TM technique is a simple mental procedure that is categorized in the automatic self-transcending category of meditation practices. It is automatic in that it does not involve any concentration or control. It allows the mental activity to settle down in a spontaneous and natural manner during a process called transcending, or going beyond, until it reaches a state beyond conscious thinking. Correspondingly, the body settles down to a deep state of rest which allows stress to dissolve and the nervous system to rejuvenate The effortless nature of the TM practice coupled with the vast research supporting its efficacy, its systematic standardized teaching program and the fact that it does not involve any belief or change in one's lifestyle made it the choice intervention for this research.
Primary Outcome Measure Information:
Title
Maslach Burnout Inventory
Description
measures burnout level
Time Frame
change from baseline burnout level at four months
Secondary Outcome Measure Information:
Title
Beck Depression Inventory
Description
measures depression level
Time Frame
change from baseline depression level at four months
Title
Insomnia Severity Index
Description
measures insomnia level
Time Frame
change from baseline insomnia level at four months
Title
Perceived Stress Scale
Description
measures level of perceived stress
Time Frame
change from baseline perceived stress level at four months
Title
Brief Resilience Inventory
Description
measures resilience level
Time Frame
change from baseline resilience level at four months
Other Pre-specified Outcome Measures:
Title
Personal Interview with researcher
Description
qualitative assessment
Time Frame
baseline, 4-months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Have an MD degree Be an academic attending physician at the Loyola Chicago School of Medicine or Edward Hines, Jr. VA Hospital Commit to attend all required sessions for learning the Transcendental Meditation (TM)technique and monthly follow-ups Agree to practice TM twice daily for 20 minutes for the 4-month study period Agree to complete both pre-and post-testing (at 1-month and 4-months) including both the entry and exit interviews. Exclusion Criteria: current suicidal ideation, previous instruction in the TM technique -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marie Loiselle, PhD
Organizational Affiliation
Outside Researcher
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Gregory Gruener, MD
Organizational Affiliation
Vice-Dean of Education
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Carla L Brown, PhD
Organizational Affiliation
Adjunct Professor
Official's Role
Principal Investigator
Facility Information:
Facility Name
Loyola University Stritch School of Medicine
City
Maywood
State/Province
Illinois
ZIP/Postal Code
60153
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
all that underlie results in a publication
IPD Sharing Time Frame
Will be available six months after publication
IPD Sharing Access Criteria
To be determined

Learn more about this trial

Effects of Transcendental Meditation on Physician Burnout and Depression

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