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Sleep Hygiene for Primary Insomnia (CEBATI Trial)
N/A
Waitlist Available
Led By Max Hines, Ph.D
Research Sponsored by Pacific Institute of Medical Sciences
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, an average of 1 year
Awards & highlights
CEBATI Trial Summary
This trial is comparing four different types of treatments (Cognitive Behavior Therapy for Insomnia (CBT-I); Focus of Attention (FOA); Combined CBT-I and FOA; and Sleep Hygiene (control group)) to see which is most effective in treating insomnia. The study is open label, meaning that participants know what treatment they are receiving, and is randomized, meaning that participants are assigned to a treatment group by chance. The study involves 6 weekly in-person sessions, and participants are asked to assess the benefits they receive from the intervention.
Eligible Conditions
- Primary Insomnia
CEBATI Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion, an average of 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average of 1 year
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Self Report Sleep Measures
Secondary outcome measures
Insomnia Severity Index
CEBATI Trial Design
4Treatment groups
Active Control
Group I: Sleep HygieneActive Control4 Interventions
Participants receive 6 one hour in person behavioral psycho-intervention sessions from a treatment provider.
Group II: Combined-CBT-I and FOA GroupActive Control4 Interventions
Participants receive 6 one hour in person behavioral psycho-intervention sessions from a treatment provider.
Group III: Cognitive Behavior Therapy-InsomniaActive Control4 Interventions
Participants receive 6 one hour in person behavioral psycho-intervention sessions from a treatment provider.
Group IV: Focus Of AttentionActive Control4 Interventions
Participants receive 6 one hour in person behavioral psycho-intervention sessions from a treatment provider.
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Who is running the clinical trial?
Pacific Institute of Medical SciencesLead Sponsor
Max Hines, Ph.DPrincipal InvestigatorPuget Sound Psychiatry center
Frequently Asked Questions
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