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Clinical Trials/NCT06465680
NCT06465680
Completed
N/A

Intern Health Study: 2024 Cohort Micro-Randomized Trial

University of Michigan2 sites in 1 country1,047 target enrollmentJuly 1, 2024

Overview

Phase
N/A
Intervention
Intern Health Study behavioral change mobile notification
Conditions
Depression
Sponsor
University of Michigan
Enrollment
1047
Locations
2
Primary Endpoint
Average daily mood
Status
Completed
Last Updated
yesterday

Overview

Brief Summary

The aim of this trial is to evaluate the efficacy of an intervention (delivered through a smartphone) for improving the mood, physical activity, and sleep of medical interns.

Detailed Description

Due to their high stress workloads, medical interns suffer from depression at higher rates than the general population. Interns also tend to have lower sleep and decreased physical activity. The goal of this trial is to evaluate the efficacy of a mobile health intervention intending to help improve the mental health of medical interns. The intervention sends mobile phone notifications which aim to help interns improve their mood, maintain physical activity, and obtain adequate sleep during their internship year. The primary aim of the study is to evaluate how notifications affect participants' weekly mood, as measured through a daily one question mood survey. The second primary aim of the study is to evaluate how notifications affect participants' long-term mental health, as measured by the Patient Health Questionnaire. The first secondary aim is to evaluate how mood notifications affect participants' weekly mood. The second secondary aim is to evaluate how activity notifications affect participants' weekly step count. The third secondary aim is to evaluate how sleep notifications affect participants' weekly sleep duration. In order to better optimize notification delivery, the final aim (exploratory) is to understand moderators of these effects. Moderators of interest are previous week's mood, previous week's step count, previous week's sleep duration, study week, sex, previous history of depression, and baseline neuroticism.

Registry
clinicaltrials.gov
Start Date
July 1, 2024
End Date
June 30, 2025
Last Updated
yesterday
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Srijan Sen

Research Professor

University of Michigan

Eligibility Criteria

Inclusion Criteria

  • Medical intern during the 2024-2025 internship year
  • iPhone or Android phone user
  • Logged into the Intern Health Study mobile app, completed consent, and filled out baseline survey by June 30 prior to the start of intern year

Exclusion Criteria

  • Not provided

Arms & Interventions

Within-participant micro-randomization

Each day in the study, with probability .5 for each, a participant is randomized to receive a notification that day or no notification that day. If a participant is assigned to receive a notification that day, 1 message set will be randomly selected from a pool of 358 core message sets. Each core message set will be comprised of 4 messages containing comparable content, however they will be tailored based on the participant's wearable (steps, sleep) or mood data for the specified time interval (7 days, 30 days, since the start of internship) as follows: 1) no data, 2) low, 3) moderate, or 4) high.

Intervention: Intern Health Study behavioral change mobile notification

Outcomes

Primary Outcomes

Average daily mood

Time Frame: Daily, through study completion at the end of intern year (1 year)

Through the mobile app, participants enter a mood score (scale 1 - 10) every day of the study. 1 corresponds to lowest mood and 10 corresponds to highest mood.

Average daily step count

Time Frame: Daily, through study completion at the end of intern year (1 year)

Participant's daily step counts are recorded through a fitness tracker. High step counts are considered a positive outcome as it indicates more physical activity.

Average nightly sleep duration

Time Frame: Daily, through study completion at the end of intern year (1 year)

Participant's nightly sleep duration (in minutes) is recorded through a fitness tracker. High sleep duration is considered a positive outcome.

Patient Health Questionnaire-9 (PHQ-9)

Time Frame: Quarterly (every 3 months for 1 year)

Prior to the start of the intervention and at quarterly intervals throughout internship year, all participants complete the Patient Health Questionnaire 9. High scores on the PHQ-9 correspond to a larger number of depressive symptoms.

Study Sites (2)

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