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Testing an Evidence-Based Program for Clinician Burnout

Testing an Evidence-Based Program for Physician and Nurse Burnout

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06145425
Enrollment
106
Registered
2023-11-24
Start date
2023-03-15
Completion date
2024-10-14
Last updated
2025-05-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burnout

Keywords

Burnout, Mindfulness, Physicians, Nurses, Resident Physicians

Brief summary

The goal of this clinical trial is to pilot test an app-based mindfulness training program in reducing burnout in physicians and nurses.

Detailed description

The main question\[s\] it aims to answer are: PRIMARY AIM: Determine if the app-based training reduces the level of cynicism (i.e., one of the two main dimensions of burnout). SECONDARY AIM: Determine if the app-based training reduces the level of emotional exhaustion (i.e. one of the two main dimensions of burnout), anxiety, worry, depression and intolerance of uncertainty. Determine if the app-based training increases self-compassion, non-reactivity and non-judging about inner experiences. Participants will be asked to: * Use an app-based mindfulness training program * Complete online surveys at baseline, immediately post-intervention and 1 month after the post-intervention as follow up

Interventions

The program is delivered via a smartphone-based platform, which includes 7 mindfulness-based modules of about 15 minutes of brief didactic and experience-based mindfulness training (audio files).

Sponsors

Peter G. Peterson Foundation
CollaboratorUNKNOWN
Brown University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

3 single groups: physicians, resident physicians and nurses

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Being a physician, resident physician or nurse * Able to speak English because all study activities will be conducted in English. * 18+ years * direct patient care

Exclusion criteria

* If using psychotropic medication - not on a stable dosage at least 6 weeks

Design outcomes

Primary

MeasureTime frameDescription
Changes in cynicismcollected at baseline, immediately post-intervention and one month later as follow upThe dimension of cynicism in the Maslach Burnout Inventory (MBI) cynicism. The MBI is a validated 22-item self-report measure of risk of burnout. Items are rated on a 7-point Likert scale ranging from 0 (never) to 6 (every day). The investigators will use only one single-item measure of cynicism that was included from the Maslach Burnout Inventory (MBI).

Secondary

MeasureTime frameDescription
The dimension of emotional exhaustion in the Maslach Burnout Inventory (MBI).collected at baseline, immediately post-intervention and one month later as follow upThe MBI is a validated 22-item self-report measure of risk of burnout. Items are rated on a 7-point Likert scale ranging from 0 (never) to 6 (every day). The investigators will use only one single-item measure of emotional exhaustion that was included from the Maslach Burnout Inventory (MBI).
Generalized Anxiety Disorder 7-items (GAD-7).collected at baseline, immediately post-intervention and one month later as follow upThe GAD-7 is a validated 7-item measure of anxiety rated on a 4-point Likert scale ranging from 0 (Not at all sure) to 3 (Nearly every day).
Five Facet Mindfulness Questionnaire (FFMQ) non-reactivity scale.collected at baseline, immediately post-intervention and one month later as follow upThe non-reactivity scale is a validated subscale of the 39-item FFMQ which is a self-report psychological measure of mindfulness skills. This subscale contains 7 items which are presented on a 6-point Likert scale ranging from 1 (almost always) to 6 (almost never).
Five Facet Mindfulness Questionnaire (FFMQ) non-judging scale.collected at baseline, immediately post-intervention and one month later as follow upThe non-judging scale is a validated subscale of the 39-item FFMQ which is a self-report psychological measure of mindfulness skills. This subscale contains 8 items which are presented on a 6-point Likert scale ranging from 1 (almost always) to 6 (almost never).
Penn State Worry Questionnaire (PSWQ).collected at baseline, immediately post-intervention and one month later as follow upThe PSWQ is a validated 16-item self-report measure of worry with items presented on a 5-point Likert scale ranging from 1 (not at all typical of me) to 5 (very typical of me).
Intolerance of Uncertainty 12-item scale (IUS-12).collected at baseline, immediately post-intervention and one month later as follow upThe IUS-12 is a validated 12-item self-report measure of intolerance of uncertainty. Items are rated on a 5-point Likert scale ranging from 1 (not at all characteristic of me) to 5 (entirely characteristic of me).
Self-Compassion Scale - Short Form (SCS-SF).collected at baseline, immediately post-intervention and one month later as follow upThe SCS-SF is a validated 12-item self-report measure of self-compassion. Items are rated on a 5-point Likert scale ranging from 1 (almost never) to 5 (almost always).
Patient Health Questionnaire 2-item scale (PHQ-2).collected at baseline, immediately post-intervention and one month later as follow upThe PHQ-2 is a validated 2-item self-report measure of depression. Items are rated on a 4-point Likert scale ranging from 0 (not at all) to 3 (nearly every day).

Other

MeasureTime frameDescription
Demographics.collected at baselineAge, gender, employment, race, ethnicity

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026