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Physician Mental Health Study for Medical Trainees

Assessment of Physician Mental Health Using Voice Analysis, Physiological Metrics and Smartphone Enabled Behavioral Modification

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02950363
Enrollment
40
Registered
2016-11-01
Start date
2016-07-31
Completion date
2017-07-31
Last updated
2017-08-28

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

Conditions

Burnout Syndrome, Mental Illness

Keywords

Depression, Suicide, Anxiety disorder, Burn out, Sleep quality, Stress

Brief summary

The purpose of this study is to determine whether use of a suite of smart phone enabled mobile health devices can reduce burnout in medical trainees. Such applications can then be used in more general populations with the same goal in mind.

Detailed description

Wearable sensors and mental health platforms delivered via smartphones offer an opportunity to passively and actively acquire quantifiable signs and symptoms related to mental health status. These features include both physiological and cognitive performance measures. Collectively they serve as a set of metrics whereby an estimation of a person's mental state can be gauged. Additionally, use of these platforms allows those who are identified as high risk for mental illness to have targeted therapy delivered via their smartphone and if necessary connected with a suitable healthcare provider. Applications of such technology platforms serve to potentially reduce the substantial morbidity and mortality in a population at increased risk for mental illness and burnout.

Interventions

None listed

Sponsors

The Scripps Research Institute
CollaboratorOTHER
Scripps Translational Science Institute
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Trainee Physician at Scripps Green Hospital or Clinic. * Older than 18 years. * Must be reliable, cooperative and willing to comply with all protocol-specified procedures. * Able to understand and grant informed consent * Have a pre-existing smart phone capable of running all study software.

Exclusion criteria

* Has a significant medical condition that in the investigator's opinion may interfere with the study subject's optimal participation in the study. * Known mental health condition including diagnosis of depression, schizophrenia, suicidality or anxiety disorder. * Does not have suitable smart phone to allow all relevant software to run.

Design outcomes

Primary

MeasureTime frameDescription
The primary endpoint is change in Maslach Burnout Inventory (MBI) over a 16 week period as measured at time points Week 0 (Baseline), 4, 10, 16.Week 0 (Baseline), 4, 10, 16Maslach Burnout Inventory

Secondary

MeasureTime frameDescription
Change in PHQ9 Score - (Raw score - No units) as measured at time points Week 0 (Baseline), 4, 10, 16.Week 0 (Baseline), 4, 10, 16Change in PHQ9 Score over 3 months.
Relationship of absolute PHQ9 Score at weeks 4, 10 & 16 to a series of biometrics as described below:Weeks 4, 10 & 16Average, following measurement of score: total time (Hours & Minutes) slept/night for week % sleep score (to Oura Ring App) per night for week min. overnight lowest heart rate (Beats per minute) per night for week Total time of per night for week: deep sleep (Hours & Minutes) light sleep (Hours & Minutes) REM sleep (Hours & Minutes) waking (Hours & Minutes) sleep latency (Hours & Minutes) % readiness score (% Measure native to Oura Ring App) Daily number of minutes of: focus (measured by Spire App) for week tension (measured by Spire App) for week calm (measured by Spire App) for week activity (measured by Spire App) for week inactivity (measured by Spire App) for week daily calories burned (measured by Spire App) for week Weekly # of (measured by the Beyond Verbal App): positive mood recordings negative mood recordings neutral mood recordings weekly arousal, temper, and valance score
Relationship of MBI score - 3 sub scales at weeks 4, 10 & 16 to a series of biometrics as described below:Weeks 4, 10 & 16Average, following measurement of score: total time (Hours & Minutes) slept/night for week % sleep score (to Oura Ring App) per night for week min. overnight lowest heart rate (Beats per minute) per night for week Total time of per night for week: deep sleep (Hours & Minutes) light sleep (Hours & Minutes) REM sleep (Hours & Minutes) waking (Hours & Minutes) sleep latency (Hours & Minutes) % readiness score (% Measure native to Oura Ring App) Daily number of minutes of: focus (measured by Spire App) for week tension (measured by Spire App) for week calm (measured by Spire App) for week activity (measured by Spire App) for week inactivity (measured by Spire App) for week daily calories burned (measured by Spire App) for week Weekly # of (measured by the Beyond Verbal App): positive mood recordings negative mood recordings neutral mood recordings weekly arousal, temper, and valance score

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026