CClinicalTrials.gg
CompletedNCT02846077Updated Jul 11, 2018

Multi-scale Modeling of Sleep Behaviors in Social Networks

An observational study in Healthy Volunteers, sponsored by Brigham and Women's Hospital. Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-07-11.

Sponsored by Brigham and Women's Hospital · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
729
Ages
18 Years and older
Sex
All
01

Study summary

The project is designed to document in college undergraduates the relationships among sleep/wake timing and duration, use of mobile phones and other electronic devices, food timing and content, self-reported mood and physiological measures.

Read the detailed description

College undergraduates are studied in cohorts of \~ 50 in fall or spring semesters. They complete diaries once in the morning and once in the evening about sleep/wake timing, timing of social and school activities, and mood. They wear physiological sensors. They install (1) an application on their mobile phone that tracks timing, duration and de-identified sender/recipient of phone calls and text messages, use of internet or apps (but not the content or names of those internet sites and apps) and (2) meal content and timing. They also spend at least one overnight session providing saliva samples for later assay for hormones.

02

Conditions studied

  • Healthy Volunteers

Keywords

  • sleep
  • social networks
  • undergraduates
  • mood
  • circadian rhythms
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In context

Lead sponsor

Brigham and Women's Hospital is the lead sponsor of 1,236 studies on the registry; 224 are open to participants now.

Of its 116 completed or terminated interventional studies of FDA-regulated products, 64 (55%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

College undergraduates

Inclusion criteria

  • undergraduate at institution at which we have permission to perform study
  • owning a mobile device on which the phone app can be installed
  • ability to wear the wrist-worn sensors

Exclusion criteria

Exclusion Criteria:

  • no travel outside one time zone starting approximately 2 weeks before monitoring begins through end of approximately one month of monitoring.
  • participation in a prior group studied
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
729 participants (actual)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • College students

    College students will be monitored and will complete online surveys, install apps on their mobile phones, wear physiological sensors and provide saliva samples for later assay.

    Other: No intervention. Observation only

Interventions

  • OtherNo intervention. Observation only

    No intervention. Observation only

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What researchers measure

Primary outcomes

  1. Timing of sleep and wake

    Timing of self-reported sleep onset and wake onset

    Time frame: Approximately one month

  2. Timing of phone use (e.g., mobile phone calls, text messages, applications and internet use)

    Timing of phone use (e.g, mobile phone calls, text messages, applications and internet use)

    Time frame: Approximately one month

Secondary outcomes

  1. Mood

    Self-reported mood using a linear non-numeric scale

    Time frame: Approximately one month

  2. Activity levels

    Activity levels collected every minute using a wrist-worn device

    Time frame: approximately one month

  3. Light exposure levels

    Light exposure levels collected every minute using a wrist-worn device

    Time frame: approximately one month

  4. Food choice

    Content of food

    Time frame: approximately one month

  5. Circadian phase

    Calculated time of melatonin phase as a marker of circadian rhythms

    Time frame: one day

  6. Electrodermal activity

    Electrodermal activity as measured using a wrist-worn device

    Time frame: approximately one month

  7. Timing of meals

    Time meals are eaten

    Time frame: approximately one month

07

Study locations

1 site
  • Brigham and Women's Hospital
    Boston, Massachusetts 02115, United States
08

References and documents

Publications

  • Fischer D, McHill AW, Sano A, Picard RW, Barger LK, Czeisler CA, Klerman EB, Phillips AJK. Irregular sleep and event schedules are associated with poorer self-reported well-being in US college students. Sleep. 2020 Jun 15;43(6):zsz300. doi: 10.1093/sleep/zsz300. PubMed 31837266 ↗
  • McHill AW, Phillips AJ, Czeisler CA, Keating L, Yee K, Barger LK, Garaulet M, Scheer FA, Klerman EB. Later circadian timing of food intake is associated with increased body fat. Am J Clin Nutr. 2017 Nov;106(5):1213-1219. doi: 10.3945/ajcn.117.161588. Epub 2017 Sep 6. PubMed 28877894 ↗

Individual participant data

Plan to share: Undecided

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 11, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02846077
Lead sponsor
Brigham and Women's Hospital
Collaborators
Massachusetts Institute of Technology, Harvard University
Responsible party
Elizabeth B. Klerman (Associate Professor, Brigham and Women's Hospital) — Principal investigator
First posted
Jul 27, 2016
Start date
Sep 2013
Primary completion
Jun 2018
Completion
Jun 2018
Last update
Jul 11, 2018

Study contacts

Elizabeth B Klerman, MD PhD
principal investigator · Brigham and Women's Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2018. You cannot join it, but the record below documents what was studied.

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