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Cognitive Behavioral Therapy and Trazodone Effects on Sleep and Blood Pressure in Insomnia
Sponsor: Milton S. Hershey Medical Center
Summary
Individuals who have insomnia with short sleep duration (ISS) differ from individuals who have insomnia with normal sleep duration (INS) in terms of health risks (i.e., hypertension) and treatment response. This study will examine whether patients with ISS and INS demonstrate a differential response to two common insomnia treatments. One is behavioral, Cognitive Behavioral Therapy for Insomnia (CBT-I). The other is a widely prescribed, non-habit-forming medication, trazodone used at a low dose. The investigators' findings could lead to evidence-based treatment guidelines that help clinicians more effectively match treatments to insomnia patients and reduce associated health problems.
Official title: Cognitive Behavioral Therapy and Trazodone Effects on Sleep and Blood Pressure in Insomnia Phenotypes Based on Objective Sleep Duration: A Sequential Cohort/Randomized Controlled Trial
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
600
Start Date
2024-03-20
Completion Date
2028-05-31
Last Updated
2025-11-10
Healthy Volunteers
No
Interventions
Cognitive Behavioral Treatment for Insomnia (CBT-I)
Subjects will receive therapy for 8 weeks
Trazodone
Non-remitting subjects will receive Trazodone (dosage) for 8 weeks
Placebo
Non-remitting subjects will receive placebo for 8 weeks
Locations (4)
National Jewish Health
Denver, Colorado, United States
Penn State University
Hershey, Pennsylvania, United States
University of Pittsburgh
Pittsburgh, Pennsylvania, United States
Université Laval
Québec, Quebec, Canada