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| Descriptive Information Fields | |||||||||
| Brief Title † | Improving Sleep and Psychological Functioning in People With Depression and Insomnia | ||||||||
| Official Title † | Hypnotics in the Treatment of Psychiatric Disorders | ||||||||
| Brief Summary | This study will evaluate the safety and effectiveness of treatment with both a sleeping pill and antidepressant medication in improving sleep and psychological functioning in people with depression and insomnia. |
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| Detailed Description | Chronic insomnia is one of the most common symptoms that individuals experience during a major depressive episode. Insomnia may lead to increased risk for recurrence of major depression, as well as poor quality of life and increased risk of suicide. Studies have shown that treating insomnia during a major depressive episode may not only help reduce symptoms of major depression during the day, but also improve an individual's general quality of life. Thus, sleeping pills, also known as hypnotics, are commonly prescribed for people with psychiatric disorders. However, little is known about the safety and efficacy of combining sleeping pills with antidepressant medications. This study will evaluate the safety and effectiveness of treatment with both a sleeping pill and antidepressant medication in improving sleep and psychological functioning in people with depression and insomnia. Participants in this double-blind study will first receive fluoxetine, an antidepressant medication, for 1 week. Participants whose symptoms of insomnia subside after this initial week will continue on fluoxetine for the duration of the study and will not receive sleeping pills. Those who do not experience an improvement in their symptoms of insomnia after 1 week will be randomly assigned to receive either placebo or eszopiclone, which is a sleeping pill, in addition to fluoxetine. All treatments will be given for 8 weeks. Participants will attend study visits at various points throughout the treatment phase. Follow up visits will occur periodically over the next 4 months. Assessments will include physiological measures during sleep, mood, suicidal thinking, quality of life and actigraphy, which measures the amount of movement during sleep. |
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| Study Phase | Phase IV | ||||||||
| Study Type † | Interventional | ||||||||
| Study Design † | Treatment, Randomized, Double Blind (Subject, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Efficacy Study | ||||||||
| Primary Outcome Measure † | "Role Functioning" and "Relation to Self/Others" Basis-32 subscale ratings [ Time Frame: Measured weekly for 9 weeks ] [ Designated as safety issue: No ] Quality of life ratings, as measured by the Quality of Life Enjoyment and Satisfaction Questionnaire (Q-LES-Q) [ Time Frame: Measured weekly for 9 weeks ] [ Designated as safety issue: No ] |
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| Secondary Outcome Measure † | Subjective sleep symptoms (perceived sleep onset latency, perceived total sleep time, number of awakenings, final rising time, and the presence and duration of any naps the prior day) [ Time Frame: Measured weekly for 10 weeks ] [ Designated as safety issue: No ] Insomnia symptoms, as measured by the Insomnia Severity Index (ISI) [ Time Frame: Measured weekly for 10 weeks ] [ Designated as safety issue: No ] |
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| Condition † | Sleep Initiation and Maintenance Disorders Depression |
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| Intervention † | Drug: Eszopiclone Drug: Fluoxetine Drug: Placebo |
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| MEDLINE PMIDs | 10733688, 10394611 | ||||||||
| Links | Click Here for More Information on This Study at The American Insomnia Association [AIA] Home Page ![]() |
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| Recruitment Information Fields | |||||||||
| Recruitment Status † | Recruiting | ||||||||
| Enrollment † | 96 | ||||||||
| Start Date † | October 2005 | ||||||||
| Completion Date | December 2008 | ||||||||
| Eligibility Criteria † | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||||||
| Ages | 18 Years to 70 Years | ||||||||
| Accepts Healthy Volunteers | No | ||||||||
| Contacts †† |
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| Location Countries † | United States | ||||||||
| Administrative Information Fields | |||||||||
| NCT ID † | NCT00247624 | ||||||||
| Organization ID | R34 MH70821 | ||||||||
| Secondary IDs †† | DSIR 83-ATSO | ||||||||
| Study Sponsor † | National Institute of Mental Health (NIMH) | ||||||||
| Collaborators †† | |||||||||
| Investigators † |
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| Information Provided By | National Institute of Mental Health (NIMH) | ||||||||
| Verification Date | February 2008 | ||||||||
| First Received Date † | October 31, 2005 | ||||||||
| Last Updated Date | March 17, 2008 | ||||||||