Pilot Sleep Extension and Mood

Description

The goal of this interventional study is to learn if a digital sleep extension intervention can improve sleep and mood in young urban adults with mood symptoms. The main questions it aims to answer are: Will this intervention improve sleep? Will this intervention improve mood? Does the effect of this intervention change based on environmental factors like noise and light pollution? Researchers will compare participants receiving the sleep intervention to participants receiving a "general healthy living" intervention to see if outcome are different across groups. Participants will: * receive 6 weeks of brief once weekly telephone coaching and read once weekly educational content * have their sleep monitored daily with a FitBit and Somnofy sleep device and during the 6-week intervention period * respond to questionnaires at the start of the intervention, halfway through the intervention, at the end of the intervention, and finally 4 weeks after completing the intervention

Conditions

Internalizing Mental Health Symptoms, Sleep Problems

Study Overview

Study Details

Study overview

The goal of this interventional study is to learn if a digital sleep extension intervention can improve sleep and mood in young urban adults with mood symptoms. The main questions it aims to answer are: Will this intervention improve sleep? Will this intervention improve mood? Does the effect of this intervention change based on environmental factors like noise and light pollution? Researchers will compare participants receiving the sleep intervention to participants receiving a "general healthy living" intervention to see if outcome are different across groups. Participants will: * receive 6 weeks of brief once weekly telephone coaching and read once weekly educational content * have their sleep monitored daily with a FitBit and Somnofy sleep device and during the 6-week intervention period * respond to questionnaires at the start of the intervention, halfway through the intervention, at the end of the intervention, and finally 4 weeks after completing the intervention

Sleep Extension to Improve Mood in Young Urban Adults

Pilot Sleep Extension and Mood

Condition
Internalizing Mental Health Symptoms
Intervention / Treatment

-

Contacts and Locations

Chicago

University of Illinois Chicago, Chicago, Illinois, United States, 60612

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Age 18 to 30
  • * Have internalizing symptoms (e.g., depression, anxiety, stress)
  • * Have sleep concerns
  • * Sleep less than 7 hours per night
  • * Have perceived neighborhood disorder
  • * Smart phone that can run Somnofy app
  • * Access to Wifi in their home
  • * High risk for obstructive sleep apnea
  • * Significant medical morbidities or psychiatric problem, or chronic substance use
  • * Non-English speaking (unable to participate in therapy or questionnaire)
  • * Taking medications for sleep
  • * An insomnia disorder
  • * Traveling for 2 weeks or more during the 10-week study period (due to loss of data from participants not sleeping in their home where the Somnofy device has been set up)
  • * Employed with rotating shift or night work

Ages Eligible for Study

18 Years to 30 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Illinois at Chicago,

Jennifer Duffecy, PhD, PRINCIPAL_INVESTIGATOR, University of Illinois Chicago

Study Record Dates

2025-09-01