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Behavioral Intervention

Smartphone Intervention for Intern Health (IHS Trial)

N/A
Waitlist Available
Research Sponsored by University of Michigan
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up daily, through study completion at the end of intern year (1 year)
Awards & highlights

IHS Trial Summary

This trial will test whether a smartphone intervention can help improve the mood, physical activity, and sleep of medical interns.

Who is the study for?
This trial is for medical interns in the 2022-2023 or 2023-2024 years who use an iPhone or Android. Participants must log into the Intern Health Study app, complete consent, and fill out a baseline survey by June 30 before their intern year starts.Check my eligibility
What is being tested?
The study tests whether a behavioral change notification sent through a mobile app can improve mood, increase physical activity, and enhance sleep quality among medical interns.See study design
What are the potential side effects?
Since this intervention involves behavioral notifications on smartphones rather than medication, traditional side effects are not expected. However, participants may experience changes in behavior or mood.

IHS Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~daily, through study completion at the end of intern year (1 year)
This trial's timeline: 3 weeks for screening, Varies for treatment, and daily, through study completion at the end of intern year (1 year) for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Average daily mood
Average daily step count
Average nightly sleep duration
+1 more

IHS Trial Design

1Treatment groups
Experimental Treatment
Group I: Within-participant micro-randomizationExperimental Treatment1 Intervention
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 60 message sets. There are 2 types of message sets: 1) Support and 2) Consequences. If a participant is assigned to receive a Support message set, they will be randomized to receive either the Emotional or Practical Support version. If a participant is assigned to receive a Consequences message set, they will be randomized to receive either the Gain Framed or Loss Framed version.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Intern Health Study behavioral change mobile notification
2018
N/A
~2140

Find a Location

Who is running the clinical trial?

University of MichiganLead Sponsor
1,794 Previous Clinical Trials
6,371,354 Total Patients Enrolled
67 Trials studying Depression
66,561 Patients Enrolled for Depression

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is recruitment for this research still ongoing?

"According to clinicaltrials.gov, the trial is currently not recruiting participants and has been edited as of July 22nd 2022. Sadly, applicants are unable to join in this study but there are over a thousand other studies that require volunteers at present."

Answered by AI

Who else is applying?

What state do they live in?
Michigan
How old are they?
18 - 65
What site did they apply to?
University of Michigan
What portion of applicants met pre-screening criteria?
Met criteria
~223 spots leftby Jun 2024