VA Palo Alto Health Care System, Palo Alto, CA
Palo Alto, California, 94304-1207, United States
NCT Number: NCT03261674
The purpose of this clinical trial is to assess the relative efficacy of two non-pharmacological interventions for insomnia in Veterans suffering from chronic mild traumatic brain injury (mTBI).
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Interventional
Not applicable
Palo Alto, California, 94304-1207, United States
Insomnia is a serious health problem in Veterans suffering from chronic Traumatic Brain Injury (TBI) and often associated with extensive prescription of sleeping medications. Although safer, even the latest "sleeping pills" can lead to daytime impairment and risk of abuse. Thus non-pharmacological treatments for insomnia have been pursued as alternatives to medications. This trial will compare the relative efficacy of Cognitive Behavioral Therapy for Insomnia (CBT-I) and Arousal-Based Therapy for Insomnia (ABT-I).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Sleep-Related
Neuropsychiatric
Medical
Cognitive Behavioral Therapy for Insomnia (CBT-I)
Arousal-Based Therapy for Insomnia (ABT-I)
Time frame: Change from baseline at week 8 after treatment
The primary outcome measure is the Veteran's subjective experience of severity of insomnia measured with the Insomnia Severity Index (ISI). The ISI has been shown to be a reliable subjective measure of insomnia severity as well as a sensitive measure of symptom change. This 7-item instrument results in total scores ranging from 0 to 28, with higher scores indicating more severe symptoms. Scores above 15 indicate clinical insomnia, and scores above 22 indicate severe symptoms.
VA Office of Research and Development
Fed
Cognitive Behavioral Therapy for Insomnia in Chronic Traumatic Brain Injury
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