← Eichor
Study identifier: NCT06779149 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Efficacy of CBT-I and Lemborexant Medication for Different Subtypes of Chronic Insomnia

Condition: Insomnia Disorder  ·  Sponsor: Laval University

PhaseNA
Planned participants90
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The primary aims of this study is to contrast the effectiveness of CBT-I and pharmacotherapy (lemborexant) compared to placebo on sleep and mental health outcomes in people with insomnia disorder and anxiety/depressive symptoms. In addition, the study will evaluate whether insomnia phenotypes (i.e., +/- 6hrs of sleep) at baseline moderate the effectiveness of the intervention on both sleep and mental health outcomes.

This description comes directly from the study's public registry record.

Talk to the study team

Manon Lamy  ·  418-656-2131  ·  manon.lamy@psy.ulaval.ca

Always discuss trial participation with your own doctor first.

Locations (1)

Université Laval Centre d'étude des troubles du sommeilQuébec, Quebec, CanadaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06779149