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NCT Number: NCT05239429

Improving the Mental Health and Well Being of Healthcare Providers Through the Transcendental Meditation Technique

The level of stress-related disorders experienced by Healthcare Providers (HCPs) has increased due to the recent COVID-19 Pandemic, impacting patient care and provider shortages. This trial aims to evaluate the use of the Transcendental Meditation Technique in improving burnout and wellbeing of HCPs over a 3-month trial period.

A total of 130 HCPs will be recruited from participating Miami hospitals, with 65 HCPs receiving training in the use of the Transcendental Meditation Technique. The remaining participants will be part of a matched control group and will not receive any training. Study outcomes will be assessed at baseline, 2 weeks, 1 month, and 3 months.

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Key information

Conditions

Burnout Behavior Behavioral Symptoms Burnout, Psychological Dyssomnias Insomnia Mental Disorders Nervous System Diseases Sleep Disorders, Intrinsic Sleep Initiation and Maintenance Disorders Sleep Wake Disorders Stress, Psychological Well Being

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The Center for Clinical and Cosmetic Research

Aventura, Florida, 33180, United States

About this study

This parallel population study aims to optimize and evaluate Healthcare Provider (HCP) wellness and performance through an evidence-based stress reduction program, Transcendental Meditation.

Transcendental Meditation (TM) has been found to be effective in reducing adverse mental health outcomes, including burnout, emotional exhaustion, depression, anxiety, insomnia, and trauma symptom severity. It is a mind-body program that allows the practitioner to experience progressively quieter, less excited states of mental activity.

For this trail, 65 HCPs affiliated with three participating Miami hospitals (Baptist Health South Florida Hospital, Mercy Miami Hospital and Encompass Health Rehabilitation Hospital of Miami) will receive instructions in the Transcendental Meditation Technique. A control group of similar numbers of HCPs will be recruited to match, to the best extent possible, for gender, age, type of HCP (doctor, nurse, etc.), and work schedule (e.g., days, nights, etc.). The control group participants will not receive Transcendental Meditation Technique training and will continue with their usual lifestyle.

The total duration of the study period will be 3 months. Study outcomes will be assessed at baseline, 2 weeks, 1 month, and 3 months' posttest, with change in burnout, insomnia, symptom, and well-being, as measured by the corresponding indexes as the primary outcomes.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Fulltime healthcare providers, medical doctors, physician assistants, nurses or other HCPs involved in active patient care or administration of patient care (Hospital Administration).
  • 18 years or older.
  • Have treated COVID-19 patients or working at locations where COVID-19 patients are being treated.
  • Willing and able to complete both baseline and post-testing.
  • If being treated with psychoactive medications, the maintenance of a stable regimen for at least two months before enrollment.
  • In the non-control group, willing and able to dedicate the time to learning the Transcendental Meditation technique and practice it twice daily for approximately 20 minutes.

Exclusion criteria

  • Already instructed in the Transcendental Meditation technique.
  • Currently unstable psychiatric symptoms as demonstrated by self-report, medical chart, or psychiatric hospitalizations in the past six months.

Treatment and study plan

Transcendental Meditation technique

Behavioral

Participants receive one-on-one training on how to use Transcendental Meditation technique which is then practiced twice daily for approximately 20 minutes.

Primary outcomes

  1. Change in Maslach Burnout Inventory- Human Services Survey (MBI-HSS) Score from Baseline

    Time frame: Baseline, 2 weeks, 1 month, and 3 months

    The Maslach Burnout Inventory- Human Services Survey (MBI-HSS) for Medical Personnel is used to measure participant burnout.

    The scale is a 22-item inventory with a seven-point response scale of 0-6 (0=never; 6= Every day).

  2. Change from Baseline in Insomnia Severity Index (ISI) Score

    Time frame: Baseline, 2 weeks, 1 month, and 3 months

    The Insomnia Severity Index (ISI) scale contains 7 sleep-related questions to measure severity of sleep problems.

    A total score is calculated to interpret the participants level of insomnia, with a total score of 0-7 indicating no clinically significant insomnia and a score of 22-18 indicative of severe Clinical Insomnia.

  3. Change from Baseline in Brief Symptom Inventory 18 (BSI 18) Score

    Time frame: Baseline, 2 weeks, 1 month, and 3 months

    The Brief Symptom Inventory 18 (BSI 18) is a 5-point rating scale used to gather patient-reported data to measure psychological distress and psychiatric disorders.

  4. Change in Warwick-Edinburgh Mental Well Being Scale (WEMWBS) Score from Baseline

    Time frame: Baseline, 2 weeks, 1 month, and 3 months

    The Warwick-Edinburgh Mental Well Being Scale (WEMWBS) scale, covering both feeling and functioning aspects of mental wellbeing, contains 14 -items with 5 response categories, summed to provide a total score.

Sponsors and collaborators

Lead sponsor

The Center for Clinical and Cosmetic Research

Other

Collaborators

  • David Lynch Foundation

Registry information

Official study title

Improving the Mental Health & Well-Being of Healthcare Providers During the COVID-19 Pandemic: A Parallel Population Study Investigating the Reduction of Burnout and Enhancement of Well-Being Through the Transcendental Meditation Technique

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Feb 14, 2022
Registry last updated
Nov 21, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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