NCT07087119

Brief Summary

The purpose of this pilot study is to evaluate the acceptability of an artificial intelligence powered mental health support tool for mental health wellness amongst physicians in training. The primary research procedures are: The primary research procedure will be the utilization of artificial intelligence powered mental health support session through a web browser for physicians in training to address symptoms related to depression and anxiety. A pre and post intervention survey, evaluating depression symptoms with the standardized PHQ-9 questionnaire and anxiety symptoms with the standardized GAD-7 questionnaire will be conducted to assess changes in mental health wellness. The study will enroll physicians in training, including Internal Medicine residents and Gastroenterology fellows. The study includes at least 4 sessions. The total study duration for each subject is 3 months.

Trial Health

63
Monitor

Trial Health Score

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

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
7mo left

Started Jul 2025

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress58%
Jul 2025Dec 2026

First Submitted

Initial submission to the registry

June 9, 2025

Completed
1 month until next milestone

Study Start

First participant enrolled

July 21, 2025

Completed
4 days until next milestone

First Posted

Study publicly available on registry

July 25, 2025

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 20, 2026

Expected
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

July 25, 2025

Status Verified

July 1, 2025

Enrollment Period

11 months

First QC Date

June 9, 2025

Last Update Submit

July 17, 2025

Conditions

Keywords

artificial intelligencephysician in trainingmental healthwellness

Outcome Measures

Primary Outcomes (1)

  • Feasibility of using Artificial Intelligence sessions as a wellness resource

    Investigators will evaluate the percentage of participants who find the Artificial Intelligence Sessions to be easily accessible and helpful.

    3 months

Secondary Outcomes (2)

  • Prevalence of depression and anxiety in training physicians

    3 months

  • Determine work-related and home-related factors that impact trainee mental health

    3 months

Study Arms (1)

physicians in training will enroll with maintained privacy into just the study group

EXPERIMENTAL

Participants will be able to engage in artificial intelligence powered mental health support session through a web browser in private sessions

Behavioral: utilization of artificial intelligence powered mental health support session through a web browser

Interventions

utilization of artificial intelligence powered mental health support session with the software XAIA through a web browser for physicians in training to address symptoms related to depression and anxiety.

physicians in training will enroll with maintained privacy into just the study group

Eligibility Criteria

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

You may qualify if:

  • Individuals 18 years old or older are included.
  • Training physicians in Internal Medicine residency and Gastroenterology fellowship at Cedars Sinai.
  • Study is limited to Cedars-Sinai employees who are known to speak English.

You may not qualify if:

  • Active treatment of severe and uncontrolled anxiety or depression with a health care professional
  • Unwilling and or unable to participate
  • Non-English speakers.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cedars Sinai Medical Center

Los Angeles, California, 90048, United States

Location

Related Publications (4)

  • Collier VU, McCue JD, Markus A, Smith L. Stress in medical residency: status quo after a decade of reform? Ann Intern Med. 2002 Mar 5;136(5):384-90. doi: 10.7326/0003-4819-136-5-200203050-00011.

    PMID: 11874311BACKGROUND
  • Guille C, Frank E, Zhao Z, Kalmbach DA, Nietert PJ, Mata DA, Sen S. Work-Family Conflict and the Sex Difference in Depression Among Training Physicians. JAMA Intern Med. 2017 Dec 1;177(12):1766-1772. doi: 10.1001/jamainternmed.2017.5138.

    PMID: 29084311BACKGROUND
  • West CP, Tan AD, Habermann TM, Sloan JA, Shanafelt TD. Association of resident fatigue and distress with perceived medical errors. JAMA. 2009 Sep 23;302(12):1294-300. doi: 10.1001/jama.2009.1389.

    PMID: 19773564BACKGROUND
  • Dutheil F, Aubert C, Pereira B, Dambrun M, Moustafa F, Mermillod M, Baker JS, Trousselard M, Lesage FX, Navel V. Suicide among physicians and health-care workers: A systematic review and meta-analysis. PLoS One. 2019 Dec 12;14(12):e0226361. doi: 10.1371/journal.pone.0226361. eCollection 2019.

    PMID: 31830138BACKGROUND

MeSH Terms

Conditions

Psychological Well-Being

Condition Hierarchy (Ancestors)

Personal SatisfactionBehavior

Study Officials

  • Kavya Reddy, MD

    Cedars-Sinai Medical Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Barbara Hollander, MD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Masking Details
Primary Investigator and outcomes assessors will not be aware of participant information. There will only be two investigators with access to participant involvement for privacy given nature of the study. The investigators with access to participant involvement are only in place for participant safety should they need immediate help during the study. Participants will be aware of who has their information and ability to contact should they need help. However the primary investigator and investigators involved in evaluating the data will have no access to participant information.
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Program Director Gastroenterology Fellowship Director Adult Care Clinic Gastroenterology Assistant Clinical Professor, David Geffen School of Medicine at UCLA

Study Record Dates

First Submitted

June 9, 2025

First Posted

July 25, 2025

Study Start

July 21, 2025

Primary Completion (Estimated)

June 20, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

July 25, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

Participant privacy

Locations