NCT07283744

Brief Summary

Nearly 50% of the adult workforce experience adverse psychological symptoms (e.g., stress, depression, burnout, etc.) stemming from workplace stressors, with healthcare workers experiencing rates as high as 80%. Some common complaints and downstream consequences of working in high-stress healthcare occupations are elevated levels of perceived stress, depression, and burnout. These conditions have been associated with unfavorable occupational (e.g., increased medical errors), patient (e.g., increased mortality rates), and provider-related outcomes (e.g., increased rates of cardiovascular disease), imposing a heavy burden on an already stretched system. Given the impact of perceived stress, depression, and burnout on employee and patient health, a clear need exists to develop effective interventions to reduce distress and promote well-being among healthcare professionals. In particular, interventions that target processes particularly vulnerable to provider stress (e.g., compassion) are needed. The present study will evaluate the feasibility and efficacy of a mindfulness-based intervention inspired by the Buddhist Four Immeasurables practice on reducing perceived stress (primary outcome), depressive symptoms, burnout, and biological markers of inflammation, and enhancing psychological well-being and sleep quality (secondary outcomes) in 80 healthcare workers. Additionally, we will investigate several mediators (compassion, positive emotions, equanimity, and mindfulness) of intervention effects. Participants will be healthcare employees of UCLA Health. They will be enrolled in a six-week, two-arm randomized controlled trial. Participants will complete self-report questionnaires at baseline, mid-course, and post-intervention to assess study outcomes and mediators. We aim to advance the study of interventions that reduce distress and promote well-being using practices that cultivate kind feelings toward oneself and others.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
8mo left

Started Oct 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress47%
Oct 2025Jan 2027

Study Start

First participant enrolled

October 10, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

December 4, 2025

Completed
12 days until next milestone

First Posted

Study publicly available on registry

December 16, 2025

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2027

Last Updated

December 16, 2025

Status Verified

December 1, 2025

Enrollment Period

1.2 years

First QC Date

December 4, 2025

Last Update Submit

December 4, 2025

Conditions

Keywords

mindfulnesscompassionloving-kindnesshealthcare professionalstress

Outcome Measures

Primary Outcomes (1)

  • Mean Change from Baseline in Perceived Stress as Assessed by the Perceived Stress Scale

    Stress will be assessed using the ten-item Perceived Stress Scale (PSS). The PSS evaluates how often individuals appraised situations in their lives as stressful during the past month (e.g., "In the last month, how often have you been angered because of things that were outside of your control?"). Respondents respond on a five-point Likert scale from 0 (never) to 4 (very often). All scores are summed to provide a total stress score. Scores range from 0 to 40, with higher scores indicating a higher level of perceived stress. The PSS has been widely used with healthcare professional populations and has been shown to be responsive to mindfulness-based interventions.

    At baseline, mid-course at week 3, and post-intervention at week 6.

Secondary Outcomes (5)

  • Mean Change from Baseline in Depressive Symptoms as Assessed with the Center for Epidemiological Studies Depression Scale

    At baseline and post-intervention at week 6.

  • Mean Change from Baseline in Burnout as Assessed with the Maslach Burnout Inventory for Medical Personnel

    At baseline and post-intervention at week 6.

  • Mean Change from Baseline in Psychological Well-being as Assessed with the Mental Health Continuum Short Form

    At baseline and post-intervention at week 6.

  • Mean Change from Baseline in Sleep Quality as Assessed with the Insomnia Severity Index

    At baseline and post-intervention at week 6.

  • Mean Change from Baseline in Inflammation as Assessed by Circulating IL-6, IL-8, IL-10, TNF-alpha, and IFN-gamma and Molecular Analysis of Gene Expression and Signaling of 19 Pro-Inflammatory, 28 Type I Interferon Response, and 3 Antibody Synthesis Genes

    At baseline and post-intervention at week 6.

Other Outcomes (6)

  • Mean Change from Baseline in Self-compassion as Assessed with the Self-Compassion Scale

    At baseline, mid-course at week 3, and post-intervention at week 6.

  • Mean Change from Baseline in Compassion for Others as Assessed with the Compassion Scale

    At baseline, mid-course at week 3, and post-intervention at week 6.

  • Mean Change from Baseline in Positive and Negative Emotions as Assessed with the modified Differential Emotions Scale

    At baseline, mid-course at week 3, and post-intervention at week 6.

  • +3 more other outcomes

Study Arms (2)

Kindness and compassion-based meditation program

EXPERIMENTAL

Half of the participants will be randomly assigned to participate in the meditation intervention. This class will meet virtually once a week for six consecutive weeks, for one hour.

Behavioral: Building Emotional Strength Training

Waitlist control

NO INTERVENTION

Half of the participants will be randomly assigned to the waitlist control. Participants assigned to this condition will have the opportunity to attend the meditation course after data collection is complete.

Interventions

The BEST intervention was designed as a secularized version of the traditional Four Immeasurables practice to promote the distinct emotional states of loving-kindness, compassion, sympathetic joy, and equanimity. Each session provides structured training and exercises in mindfulness, including formal meditation practices and strategies for the daily informal use of mindfulness, as well as opportunity for questions and group discussion. Home practice is a key component of BEST and is particularly important for addressing stress in daily life. Participants will be instructed to practice mindfulness techniques on a daily basis, beginning with five minutes and increasing to 20 minutes, with practice prior to work or other stress-inducing situations.

Kindness and compassion-based meditation program

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of California, Los Angeles

Los Angeles, California, 90095, United States

RECRUITING

Study Officials

  • Julienne E Bower, Ph.D.

    University of California, Los Angeles, Psychology Department

    PRINCIPAL INVESTIGATOR

Central Study Contacts

J Richard T Korecki, M.A.

CONTACT

Julienne E Bower, Ph.D.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Area Chair: Health Psychology

Study Record Dates

First Submitted

December 4, 2025

First Posted

December 16, 2025

Study Start

October 10, 2025

Primary Completion (Estimated)

January 1, 2027

Study Completion (Estimated)

January 1, 2027

Last Updated

December 16, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

There is no plan to share any individual participant data (IPD) with any other researchers. Data will be reported in group form to prevent personal identification of participants. When the research has been completed, the data will be stored in a secured area of a private, locked research office. Any personal identifiers and/or codes linking the data to personal identifiers will be kept on a separate computer with password protection for reference and for future research. All personal identifiers will be kept confidential. Only identified members of the research team and the P.I. will have access to the data, identifiers and/or codes. Data with subject identifiers will not be released to any agency or persons.

Locations