Expired Study
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Atlanta, Georgia 30303


Purpose:

The proposed study will consist of a randomized controlled trial (RCT) comparing a known efficacious treatment for insomnia (CBT-I) to a sleep hygiene (SH) comparison condition.


Study summary:

The purpose of this study is to test whether a group cognitive-behavioral treatment program for insomnia (CBT-I) will help adults diagnosed with HIV to improve the quantity (number of hours) and the quality of their sleep. The PI will compare adults who participated in the CBT-I program to adults who participated in a Sleep Hygiene group, a common treatment for insomnia. The PI will look at the overall quality of life, and number of hours and quality of sleep of adults who participated in the CBT-I program versus adults in the Sleep Hygiene group. Also, the PI will draw blood to compare how the body responds to medical illnesses between adults in the CBT-I program to adults in the Sleep Hygiene group.


Criteria:

Inclusion Criteria: - English-speaking individuals - over the age of 18 years old with a diagnosis of HIV or AIDS who is receiving medical care at the Grady Health System's Infectious Disease Program (IDP) - study subjects must meet the criteria for primary or secondary insomnia as defined by the Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision - must experience difficulty initiating or maintaining non-restorative sleep for at least l month (DSM- IV-TR) - the sleep disturbance causes clinically significant impairment or distress in important areas of functioning - sleep efficiency of less than 85%, sleep disturbances that occur three or more days per week, and sleep latency (i.e., time awake after sleep onset greater than 30 minutes) Exclusion Criteria: - current substance dependence (within the past six months) - active psychosis - Bipolar I and II disorders - neurocognitive impairment and/or a current diagnosis of dementia - lack of independent housing - previous participation in a CBT-I program - employment in a job requiring shift work that impairs the ability to establish a regular sleep schedule


NCT ID:

NCT02259101


Primary Contact:

Principal Investigator
Amit Shahane, Ph.D.
Emory University


Backup Contact:

N/A


Location Contact:

Atlanta, Georgia 30303
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 21, 2017

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