Testing Utility of Commercially Available Sleep Trackers for Physician-Patient Communication
Status unconfirmed · Not applicable
Conditions studied: Insomnia
In brief
Sleep related disorders are common in primary care practice. Sleep wear related data has not been utilized to improve sleep related communication between patients and providers. The study team is conducting a randomized study to improve physical-patient communication regarding sleep through a novel intervention based upon sleep wear and the Sleeplife® app.
Key facts
- Study ID
- NCT03795129
- Run by
- Regenstrief Institute, Inc.
- People needed
- 200
- Starts
- 2018-06-10
- Expected to finish
- 2019-02-28
- Last updated by the study team
- 2019-01-07
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- 18 and older
- Have insomnia as identified by electronic record and/or a validated questionnaire
- Prescription medication for insomnia with International Classification of Disease (ICD) codes: 327.*, 780.5*, 347.*; icd-10's G47* and medications: Ambien (zolpidem), Belsomra (suvorexant), Butisol (butabarbital), Doral (quazepam), Edluar (zolpidem), Estazolam, Flurazepam, Halcion (triazolam), Hetlioz (tasimelteon), Intermezzo (zolpidem), Lunesta (eszopiclone), Restoril (temazepam), Rozerem (ramelteon), Seconal (secobarbital), Silenor (doxepin), Sonata (zaleplon), and Zolpimist (zolpidem)
- English speaking 4. Consentable in-person 5. Have access to a telephone with smart phone capabilities. (iOS/Android)
You may not qualify if…
- Not English speaking
- Have ischemic or hemorrhagic cerebrovascular disease affecting collection of study outcomes (via ICD codes I6*, 43*)
- History of dementia (via ICD codes F0*, 290*)
- History of Bipolar/Schizophrenia/Depression (via ICD codes F2*, F31*, 296*, 295*)
- History of alcohol or substance abuse (via ICD codes F1*, 304*, 303*)
- Incarcerated/Long Term Care (LTC)
- Unable to complete study questionnaires due to hearing loss or blindness
Where it is running
- Regenstrief Institute — Indianapolis, Indiana, United States (enrolling)
Full record on ClinicalTrials.gov
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