Mobile Sleep Intervention for OEF, OIF and OND Veterans
NCT ID: NCT02392000
Last Updated: 2018-04-20
Study Results
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View full resultsBasic Information
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COMPLETED
NA
38 participants
INTERVENTIONAL
2015-10-20
2016-11-16
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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WatchPAT and CBT-i Coach mobile app
Individuals use the WatchPAT sleep monitor and the CBT-i Coach app to self-manage insomnia
WatchPAT sleep monitor
Self-management of insomnia using a mobile sleep device
CBT-i Coach mobile app
Self-management of insomnia using a mobile app based on Cognitive Behavioral Therapy for Insomnia
Interventions
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WatchPAT sleep monitor
Self-management of insomnia using a mobile sleep device
CBT-i Coach mobile app
Self-management of insomnia using a mobile app based on Cognitive Behavioral Therapy for Insomnia
Eligibility Criteria
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Inclusion Criteria
* be age 21-65,
* report current insomnia as defined by an Insomnia Index Severity 40 score \> 10 5,79,
* and report insomnia duration of at least 1 month and impaired daytime functioning (as measured by endorsing Much or Very Much on ISI Item 7 about how much sleep problems interfere with daily functioning).
* In addition, eligible individuals must be willing to use a device provided by the study team (an iPod touch).
Exclusion Criteria
* periodic leg movements,
* or circadian rhythm disorder (delayed or advanced sleep phase).
* Exclusions for WatchPAT use include use of alpha blockers or short-acting nitrates,
* permanent pacemaker, or
* sustained non-sinus cardiac arrhythmias. Sleep apnea will be assessed from the WatchPAT on the first night of objective sleep testing and participants excluded from further participation if apnea is documented.
* Other exclusions include moderate to severe cognitive impairment defined by scores on the Telephone Mini Mental State Exam,
* inability to speak and read English,
* or malformation of the fingers that would preclude use of the WatchPAT device.
* In addition, individuals meeting criteria for current active psychosis, mania, suicidal ideation with plan and intent, or excessive alcohol use as determined using the AUDIT-C will be excluded from participation.
* Those with greater than mild sleep apnea as determined based on a WatchPAT-based Apnea-Hypopnea Index \[AHI\] \> 15/hour of sleep, will be withdrawn from the study and referred for sleep apnea treatment.
21 Years
65 Years
ALL
No
Sponsors
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University of Rochester
OTHER
Northeastern University
OTHER
VA Office of Research and Development
FED
Responsible Party
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Principal Investigators
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Karen S. Quigley, PhD
Role: PRINCIPAL_INVESTIGATOR
Edith Nourse Rogers Memorial Veterans Hospital, Bedford, MA
Locations
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Edith Nourse Rogers Memorial Veterans Hospital, Bedford, MA
Bedford, Massachusetts, United States
Countries
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References
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Kaitz J, Robinson SA, Petrakis BA, Reilly ED, Chamberlin ES, Wiener RS, Quigley KS. Veteran Acceptance of Sleep Health Information Technology: a Mixed-Method Study. J Technol Behav Sci. 2023;8(1):57-68. doi: 10.1007/s41347-022-00287-x. Epub 2022 Dec 13.
Reilly ED, Robinson SA, Petrakis BA, Kuhn E, Pigeon WR, Wiener RS, McInnes DK, Quigley KS. Mobile App Use for Insomnia Self-Management: Pilot Findings on Sleep Outcomes in Veterans. Interact J Med Res. 2019 Jul 24;8(3):e12408. doi: 10.2196/12408.
Other Identifiers
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PPO 14-144
Identifier Type: -
Identifier Source: org_study_id
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