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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 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average of 1 year
This trial's timeline: 3 weeks for screening, Varies for treatment, and through study completion, an average of 1 year for reporting.

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.

Find a Location

Who is running the clinical trial?

Pacific Institute of Medical SciencesLead Sponsor
Max Hines, Ph.DPrincipal InvestigatorPuget Sound Psychiatry center

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~24 spots leftby Apr 2025