Multimodal Sleep Intervention Using Wearable Technology
Status: | Recruiting |
---|---|
Conditions: | Psychiatric |
Therapuetic Areas: | Psychiatry / Psychology |
Healthy: | No |
Age Range: | 18 - 25 |
Updated: | 1/10/2019 |
Start Date: | December 7, 2018 |
End Date: | April 2021 |
Contact: | Garrett I Ash, PhD |
Email: | garrett.ash@yale.edu |
Phone: | 2034443079 |
Development of a Multimodal Sleep Intervention Using Wearable Technology to Reduce Heavy Drinking in Young Adults
This research study is examining three different components of a mobile sleep intervention:
web-based sleep hygiene advice, sleep and alcohol diary self-monitoring, and personalized
sleep and alcohol consumption feedback. The study is designed to find out which of these
components are most effective for mitigating alcohol use disorders and improving sleep
quality among young adults. The study has three parts: 1) an intake session; 2) a 2-week
treatment phase; and 3) three follow-up visits over the next 10 weeks.
web-based sleep hygiene advice, sleep and alcohol diary self-monitoring, and personalized
sleep and alcohol consumption feedback. The study is designed to find out which of these
components are most effective for mitigating alcohol use disorders and improving sleep
quality among young adults. The study has three parts: 1) an intake session; 2) a 2-week
treatment phase; and 3) three follow-up visits over the next 10 weeks.
Targeting sleep concerns may be a novel strategy for reducing increased risk of alcohol use
disorders in young adults. The current study will develop and test a mobile intervention
addressing sleep concerns in 120 heavy-drinking young adults. All participants will wear
sleep and alcohol trackers daily. Participants will be randomized to one of three
interventions. The primary intervention (60 participants) will include web-based sleep
hygiene advice + sleep/alcohol diary self-monitoring + sleep/alcohol data feedback. The
comparison interventions will be compared to matched control conditions only including these
components: (1) web-based sleep hygiene advice (30 participants) or (2) web-based sleep
hygiene advice + sleep/alcohol diary self-monitoring (30 participants). The primary objective
is to evaluate sleep intervention component feasibility, acceptability, and preliminary
efficacy on alcohol outcomes to inform a Stage II randomized trial comparing the final sleep
intervention with a standard alcohol intervention.
disorders in young adults. The current study will develop and test a mobile intervention
addressing sleep concerns in 120 heavy-drinking young adults. All participants will wear
sleep and alcohol trackers daily. Participants will be randomized to one of three
interventions. The primary intervention (60 participants) will include web-based sleep
hygiene advice + sleep/alcohol diary self-monitoring + sleep/alcohol data feedback. The
comparison interventions will be compared to matched control conditions only including these
components: (1) web-based sleep hygiene advice (30 participants) or (2) web-based sleep
hygiene advice + sleep/alcohol diary self-monitoring (30 participants). The primary objective
is to evaluate sleep intervention component feasibility, acceptability, and preliminary
efficacy on alcohol outcomes to inform a Stage II randomized trial comparing the final sleep
intervention with a standard alcohol intervention.
Inclusion Criteria:
1. 18-25 years of age;
2. report ≥ 3 heavy drinking occasions in the last 2 weeks (i.e., ≥5 drinks on 1 occasion
for men; ≥4 for women);
3. report having concerns about their sleep;
4. willing/able to complete daily sleep diaries and wear sleep and alcohol trackers;
5. report Alcohol Use Disorders Identification Test - Consumption (AUDIT-C) scores
indicative of risk of harm from drinking (i.e., ≥7 and ≥5 for men and women,
respectively)
6. read and understand English;
7. have a smartphone that can be used to sync tracker data. An estimated 86% of young
adults own a smartphone.
Exclusion Criteria:
1. history of a sleep disorder;
2. night or rotating shift work; travel beyond 2 time zones in month prior and/or planned
travel beyond 2 time zones during study participation;
3. meet criteria for an alcohol use disorder in the past 12 months that is clinically
severe defined by: a) a history of seizures, delirium, or hallucinations during
alcohol withdrawal; b) report drinking to avoid withdrawal symptoms or have had prior
treatment of alcohol withdrawal; c) have required medical treatment of alcohol
withdrawal in the past 6 months;
4. currently enrolled in alcohol or sleep treatment;
5. exhibit current psychiatric illness (i.e., bipolar disorder, schizophrenia, major
depression, panic disorder, borderline personality disorder, organic mood or mental
disorders, or suicide or violence risk) by history or psychological examination;
6. current DSM-V substance use disorder or a positive urine drug screen for opiates,
cocaine, barbiturates, benzodiazepines, amphetamines, or phencyclidine.
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