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RECRUITING
NCT06281756
EARLY_PHASE1

Cognitive Behavioral Therapy and Trazodone Effects on Sleep and Blood Pressure in Insomnia

Sponsor: Milton S. Hershey Medical Center

View on ClinicalTrials.gov

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

BEHAVIORAL

Cognitive Behavioral Treatment for Insomnia (CBT-I)

Subjects will receive therapy for 8 weeks

DRUG

Trazodone

Non-remitting subjects will receive Trazodone (dosage) for 8 weeks

OTHER

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