Impact of Sleep Workshops in College Students

NCT ID: NCT02665247

Last Updated: 2022-07-07

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

180 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-10-24

Study Completion Date

2019-11-24

Brief Summary

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The purpose of this pilot study is to assess the impact of sleep workshops on sleep, mood, anxiety and well-being measures in a sample of college students. College students have a high prevalence of sleep problems including poor sleep hygiene, volitional sleep deprivation, and insomnia. Sleep disorders in college students negatively affect mood, social functioning, physical safety, and academic performance. Rarely recognized by the students themselves, these conditions are therefore often untreated. Participants in this study will be randomly assigned to receive the College Sleep Improvement Plan (C-SIP) or a control session. Participants will be asked to track their sleep as well as complete questionnaires; a subset of participants will be asked to wear an activity monitor.

Detailed Description

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Conditions

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Sleep Insomnia Sleep Deprivation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

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.

Group Type EXPERIMENTAL

C-SIP

Intervention Type BEHAVIORAL

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.

Group Type OTHER

Dream discussion

Intervention Type OTHER

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.

Intervention Type BEHAVIORAL

Dream discussion

Participants assigned to the control group will attend sessions in which information on sleep is presented in the form of dream discussions.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Currently enrolled in classes at the NYU Washington Square campus

Exclusion Criteria

* Students previously enrolled in the "While You Were Sleeping" course at NYU
Minimum Eligible Age

18 Years

Maximum Eligible Age

25 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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NYU Langone Health

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

Countries

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United States

Other Identifiers

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15-00847

Identifier Type: -

Identifier Source: org_study_id

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