COMPLETED

Pilot Sleep Extension and Mood

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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

Official Title

Sleep Extension to Improve Mood in Young Urban Adults

Quick Facts

Study Start:2025-01-01
Study Completion:2025-11-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06675799

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.

Ages Eligible for Study:18 Years to 30 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age 18 to 30
  2. * Have internalizing symptoms (e.g., depression, anxiety, stress)
  3. * Have sleep concerns
  4. * Sleep less than 7 hours per night
  5. * Have perceived neighborhood disorder
  6. * Smart phone that can run Somnofy app
  7. * Access to Wifi in their home
  1. * High risk for obstructive sleep apnea
  2. * Significant medical morbidities or psychiatric problem, or chronic substance use
  3. * Non-English speaking (unable to participate in therapy or questionnaire)
  4. * Taking medications for sleep
  5. * An insomnia disorder
  6. * 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)
  7. * Employed with rotating shift or night work

Contacts and Locations

Principal Investigator

Jennifer Duffecy, PhD
PRINCIPAL_INVESTIGATOR
University of Illinois Chicago

Study Locations (Sites)

University of Illinois Chicago
Chicago, Illinois, 60612
United States

Collaborators and Investigators

Sponsor: University of Illinois at Chicago

  • Jennifer Duffecy, PhD, PRINCIPAL_INVESTIGATOR, University of Illinois Chicago

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-01-01
Study Completion Date2025-11-01

Study Record Updates

Study Start Date2025-01-01
Study Completion Date2025-11-01

Terms related to this study

Keywords Provided by Researchers

  • young adults
  • sleep
  • mood
  • anxiety
  • depression
  • sleep extension
  • stress

Additional Relevant MeSH Terms

  • Internalizing Mental Health Symptoms
  • Sleep Problems