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An Interactive Internet Intervention for Adults With Insomnia (SHUTi)

Primary Purpose

Insomnia, Sleep Initiation and Maintenance Disorders

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Internet Intervention
Patient Education Website
Sponsored by
University of Virginia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Insomnia focused on measuring sleep, insomnia, internet, CBT

Eligibility Criteria

21 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age between 21 and 65 years old.
  • Have sleep-onset insomnia and/or sleep maintenance insomnia (>30 minutes for at least 3 nights/week).
  • Have insomnia symptoms lasting at least 6 months.
  • Have an average total sleep time ≤ 6.5 hours.
  • Sleep disturbances (or associated daytime fatigue) cause significant distress or impairment in social, occupational, or other areas of functioning.
  • Have regular access to a computer and the Internet.
  • Reside in the United States or are US Citizens living outside the United States

Exclusion Criteria:

  • Pregnancy
  • Report of a physical illness which is deemed active, unstable, degenerative, and/or progressive, such as congestive heart failure, dementia, or acute pain.
  • Bipolar disorder as defined by a manic or hypomanic episode or treatment within the past 10 years.
  • Severe depression.
  • Endorse risk of suicide.
  • Endorse alcohol or drug abuse within the past year.
  • Presence of another untreated sleep disorder (e.g., sleep apnea, periodic leg movements).
  • Have irregular sleep schedules, with usual bedtimes earlier than 8:00pm or later than 2:00am or arising times earlier than 4:00am or later than 10:00am.
  • Current psychological treatment for insomnia.
  • Initiating psychological treatment within past 3 months.
  • Unstable medication regimen (change to schedule or dosage within past 3 months) for a medication regimen thought to impact sleep.

Sites / Locations

  • University Of Virginia Health System, Department of Psychiatry and Neurobehavioral Sciences, Division of Behavioral Health and Technology

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Internet Intervention

Patient Education Website

Arm Description

Assigned to Sleep Healthy Using the Internet (SHUTi)

Assigned to Patient Insomnia Educational Website

Outcomes

Primary Outcome Measures

Primary sleep symptoms: sleep onset latency (SOL), wake after sleep onset (WASO), insomnia severity (ISI)

Secondary Outcome Measures

Secondary sleep symptoms: sleep efficiency (SE), number of night time awakenings, sleep quality, total sleep time (TST)
Psychological distress: levels of depression, levels of anxiety, sleep-related cognitions
Health symptoms: fatigue, quality of life
Cost effectiveness: program delivery cost, participant resource utilization and costs, quality adjusted life years (QALYs)
Intervention Evaluation: perceived utility, perceived impact, intervention adherence, intervention use
Exploratory Outcome Measures: health care access, coverage and utilization

Full Information

First Posted
September 20, 2011
Last Updated
January 11, 2017
Sponsor
University of Virginia
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT01438697
Brief Title
An Interactive Internet Intervention for Adults With Insomnia
Acronym
SHUTi
Official Title
An Internet Intervention for Insomnia: Efficacy and Dissemination
Study Type
Interventional

2. Study Status

Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
October 2011 (undefined)
Primary Completion Date
October 2014 (Actual)
Study Completion Date
October 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Virginia
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will compare the efficacy of an interactive Internet intervention for adult insomnia (Sleep Healthy Using the Internet; SHUTi) to that of a static educational website to improve sleep, mood related symptoms, perceived health status, and overall quality of life.
Detailed Description
Insomnia is defined by complaints of poor sleep, as well as difficulties initiating and/or maintaining sleep more than 3 nights/week for more than 6 months. Insomnia may contribute to daytime fatigue, impaired performance, confused thinking and judgment, and difficulty with work and personal tasks. Cognitive behavioral therapy (CBT) has been found to have significant short- and long-term benefits for people with insomnia. Access to CBT for many people, however, is limited, due to the high cost of treatment and a limited number of trained professionals. Delivering CBT for insomnia via the Internet could help make it more widely available. This study will compare the effectiveness of an online CBT intervention in improving sleep, mood, and quality of life in people with insomnia to that of a static educational website. Participants in this study will be randomly assigned to receive the online CBT intervention or the static patient education website. The intervention period will last for 9 weeks. During the intervention period, participants assigned to the patient education website will be given content addressing strategies for dealing with insomnia. Those assigned to use the Internet intervention will review interactive, tailored content specific to the user's difficulties. Participants will complete questionnaires and two weeks of daily sleep diaries about their symptoms at four time points - at the beginning of the study, immediately after completing the 9 week program, 6 months later, and 12 months later.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insomnia, Sleep Initiation and Maintenance Disorders
Keywords
sleep, insomnia, internet, CBT

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
303 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Internet Intervention
Arm Type
Experimental
Arm Description
Assigned to Sleep Healthy Using the Internet (SHUTi)
Arm Title
Patient Education Website
Arm Type
Active Comparator
Arm Description
Assigned to Patient Insomnia Educational Website
Intervention Type
Behavioral
Intervention Name(s)
Internet Intervention
Other Intervention Name(s)
Sleep Healthy Using the Internet (SHUTi)
Intervention Description
Participants will spend 1-2 hours each week for 9 weeks using the Internet intervention. Users will complete daily sleep diaries as well as interactive tutorials covering the topics of sleep behaviors, sleep thoughts, sleep education, and relapse prevention. As users progress through the program they will receive tailored instructions for how to improve their sleep.
Intervention Type
Behavioral
Intervention Name(s)
Patient Education Website
Intervention Description
Participants will be given access to a relevant patient education website. It will contain material addressing the behaviors and symptoms of insomnia.
Primary Outcome Measure Information:
Title
Primary sleep symptoms: sleep onset latency (SOL), wake after sleep onset (WASO), insomnia severity (ISI)
Time Frame
Baseline, 9 weeks, 6 months, 1 year
Secondary Outcome Measure Information:
Title
Secondary sleep symptoms: sleep efficiency (SE), number of night time awakenings, sleep quality, total sleep time (TST)
Time Frame
Baseline, 9 weeks, 6 months, 1 year
Title
Psychological distress: levels of depression, levels of anxiety, sleep-related cognitions
Time Frame
Baseline, 9 weeks, 6 months, 1 year
Title
Health symptoms: fatigue, quality of life
Time Frame
Baseline, 9 weeks, 6 months, 1 year
Title
Cost effectiveness: program delivery cost, participant resource utilization and costs, quality adjusted life years (QALYs)
Time Frame
9 weeks, 6 months, 1 year
Title
Intervention Evaluation: perceived utility, perceived impact, intervention adherence, intervention use
Time Frame
9 weeks, 6 months, 1 year
Title
Exploratory Outcome Measures: health care access, coverage and utilization
Time Frame
Baseline, 9 weeks, 6 months, 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between 21 and 65 years old. Have sleep-onset insomnia and/or sleep maintenance insomnia (>30 minutes for at least 3 nights/week). Have insomnia symptoms lasting at least 6 months. Have an average total sleep time ≤ 6.5 hours. Sleep disturbances (or associated daytime fatigue) cause significant distress or impairment in social, occupational, or other areas of functioning. Have regular access to a computer and the Internet. Reside in the United States or are US Citizens living outside the United States Exclusion Criteria: Pregnancy Report of a physical illness which is deemed active, unstable, degenerative, and/or progressive, such as congestive heart failure, dementia, or acute pain. Bipolar disorder as defined by a manic or hypomanic episode or treatment within the past 10 years. Severe depression. Endorse risk of suicide. Endorse alcohol or drug abuse within the past year. Presence of another untreated sleep disorder (e.g., sleep apnea, periodic leg movements). Have irregular sleep schedules, with usual bedtimes earlier than 8:00pm or later than 2:00am or arising times earlier than 4:00am or later than 10:00am. Current psychological treatment for insomnia. Initiating psychological treatment within past 3 months. Unstable medication regimen (change to schedule or dosage within past 3 months) for a medication regimen thought to impact sleep.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karen Ingersoll, PhD
Organizational Affiliation
University Of Virginia Behavioral Health & Technology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lee M Ritterband, PhD
Organizational Affiliation
University of Virginia Behavioral Health & Technology
Official's Role
Study Director
Facility Information:
Facility Name
University Of Virginia Health System, Department of Psychiatry and Neurobehavioral Sciences, Division of Behavioral Health and Technology
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22903
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
24014057
Citation
Thorndike FP, Ritterband LM, Gonder-Frederick LA, Lord HR, Ingersoll KS, Morin CM. A randomized controlled trial of an internet intervention for adults with insomnia: effects on comorbid psychological and fatigue symptoms. J Clin Psychol. 2013 Oct;69(10):1078-93. doi: 10.1002/jclp.22032. Epub 2013 Aug 28.
Results Reference
result
PubMed Identifier
26994361
Citation
Quigg M, Gharai S, Ruland J, Schroeder C, Hodges M, Ingersoll KS, Thorndike FP, Yan G, Ritterband LM. Insomnia in epilepsy is associated with continuing seizures and worse quality of life. Epilepsy Res. 2016 May;122:91-6. doi: 10.1016/j.eplepsyres.2016.02.014. Epub 2016 Mar 2.
Results Reference
result
PubMed Identifier
27902836
Citation
Ritterband LM, Thorndike FP, Ingersoll KS, Lord HR, Gonder-Frederick L, Frederick C, Quigg MS, Cohn WF, Morin CM. Effect of a Web-Based Cognitive Behavior Therapy for Insomnia Intervention With 1-Year Follow-up: A Randomized Clinical Trial. JAMA Psychiatry. 2017 Jan 1;74(1):68-75. doi: 10.1001/jamapsychiatry.2016.3249.
Results Reference
result
Links:
URL
http://www.shuti.org
Description
Sleep Health Using the Internet intervention site
URL
http://bht.virginia.edu
Description
University of Virginia Behavioral Health & Technology research lab

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An Interactive Internet Intervention for Adults With Insomnia

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