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This research will examine the effectiveness of a 6-week online sleep program (Go! To Sleep) which provides a set of various psycho-educational materials and behavioral techniques to reduce insomnia symptoms, improve sleep, and improve quality of life.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Go! to Sleep | Active Comparator | Participants access and utilize the 6-week online program that provides a set of various psycho-educational materials and behavioral techniques to treat insomnia. |
|
| Control Group | No Intervention | No intervention provided. These participants will receive the Go! to Sleep program after the research trial has been completed (10 weeks after registration). |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Go! to Sleep | Behavioral | The online program provides various tools for the delivery of the intervention including:
|
| Measure | Description | Time Frame |
|---|---|---|
| Insomnia severity | To assess the effectiveness of the online Go! to Sleep program in improving sleep by measuring insomnia severity using the Insomnia Severity Index (ISI). | 5 months |
| Measure | Description | Time Frame |
|---|---|---|
| Insomnia symptoms | To determine if the program helps improve insomnia symptoms as measured by the Pittsburgh Insomnia Rating Scale (PIRS) | 5 months |
| Sleep pattern | To determine if the program helps improve sleep-onset latency (SOL), total sleep time (TST), waking after sleep onset (WASO) (within Go To Sleep! group analysis only) |
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Inclusion Criteria:
Age 18 to 70 years old.
Currently living in the continental United States and Canada.
Symptoms of insomnia based on the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV) definition of insomnia disorder:
Willingness to log onto the internet on a regular basis for the duration of the study (3-7 months).
Willingness and able to complete almost daily a sleep log to track sleep pattern for up to 2 months at a time (approximately 2-3 min daily).
Willingness to be in the Wait-list control group and not have access to the program for 3 months.
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Adam Bernstein, M.D. | The Cleveland Clinic | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Cleveland Clinic Foundation | Cleveland | Ohio | 44195 | United States |
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| ID | Term |
|---|---|
| D007319 | Sleep Initiation and Maintenance Disorders |
| ID | Term |
|---|---|
| D020919 | Sleep Disorders, Intrinsic |
| D020920 | Dyssomnias |
| D012893 | Sleep Wake Disorders |
| D009422 | Nervous System Diseases |
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|
| 5 months |
| Daytime Dysfunction | To determine if the program improves daytime dysfunction (Pittsburgh Sleep Quality Index subscale) | 5 months |
| Stress | To assess whether the program reduces stress as measured by the Perceived Stress Scale (PSS10) | 5 months |
| Program adherence | To assess program adherence and its relation to program effectiveness | 5 months |
| D001523 |
| Mental Disorders |