Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
180 participants
INTERVENTIONAL
2016-10-24
2019-11-24
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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C-SIP
Participants assigned to the C-SIP group will attend sessions where information about sleep is presented. In session I, information about sleep and the effects of lack of sleep will be presented. Participants will also be presented with advice and tips on how to improve sleep. Session II will focus on assisting participants overcome any barriers they faced in applying the advice they received in session I; participants will also receive additional information on sleep and sleep-related techniques.
C-SIP
In session I, information about sleep and the effects of lack of sleep will be presented. Participants will also be presented with advice and tips on how to improve sleep. Session II will focus on assisting participants overcome any barriers they faced in applying the advice they received in session I; participants will also receive additional information on sleep and sleep-related techniques.
Control Session
Participants assigned to the control group will attend sessions in which information on sleep is presented in the form of dream discussions.
Dream discussion
Participants assigned to the control group will attend sessions in which information on sleep is presented in the form of dream discussions.
Interventions
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C-SIP
In session I, information about sleep and the effects of lack of sleep will be presented. Participants will also be presented with advice and tips on how to improve sleep. Session II will focus on assisting participants overcome any barriers they faced in applying the advice they received in session I; participants will also receive additional information on sleep and sleep-related techniques.
Dream discussion
Participants assigned to the control group will attend sessions in which information on sleep is presented in the form of dream discussions.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
25 Years
ALL
Yes
Sponsors
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NYU Langone Health
OTHER
Responsible Party
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Principal Investigators
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Jess Shatkin
Role: PRINCIPAL_INVESTIGATOR
NYU Langone Medical Center
Locations
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NYU School of Medicine
New York, New York, United States
Countries
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Other Identifiers
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15-00847
Identifier Type: -
Identifier Source: org_study_id
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