Ignite Creation Date:
2024-07-17 @ 11:04 AM
Last Modification Date:
2024-10-26 @ 3:32 PM
Study NCT ID:
NCT06465680
Status:
ACTIVE_NOT_RECRUITING
Last Update Posted:
2024-07-03
First Post:
2024-06-13
Brief Title:
Intern Health Study 2024
Sponsor:
University of Michigan
Organization:
University of Michigan
Study Overview
Official Title:
Intern Health Study 2024 Cohort Micro-Randomized Trial
Status:
ACTIVE_NOT_RECRUITING
Status Verified Date:
2024-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
IHS
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 weeks mood previous weeks step count previous weeks sleep duration study week sex previous history of depression and baseline neuroticism
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 weeks mood previous weeks step count previous weeks sleep duration study week sex previous history of depression and baseline neuroticism
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None