Group Cognitive Behavioral Therapy (CBT I) Vs. Quetiapine for Residual Insomnia Impairing Recovery Among Elderly With Stable Major Affective Disorders
Study Details
Study Description
Brief Summary
The purpose of this pilot study is to assess feasibility and patient accessibility in order to design an adequately powered study to compare group cognitive behavioral therapy for insomnia (CBT-I) to quetiapine in non-demented patients aged 60 years or older with controlled bipolar disorder (I or II) or major depressive disorder who suffer from residual insomnia.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2/Phase 3 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: CBT
|
Drug: Quetiapine
Behavioral: Cogntive behavioral therapy
|
Outcome Measures
Primary Outcome Measures
- PTSQ [12 weeks]
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Age greater or equal to 60 years.
-
Patients with history of major affective disorder, including Bipolar disorder type I or type II or major depressive disorder, as assessed by the Structured Clinical Interview for DSM-IV (SCID), currently in remission.
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Difficulty starting or initiating sleep four or more times/week for at least 3 months by history.
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Total Pittsburg Sleep Quality Index >5.
Exclusion Criteria:
-
Patient in an acute mood episode as assessed by SCID
-
Patients with sleep disruptive medical problems including: sleep apnea, restless leg syndrome, periodic limb movement, parasomnia, congestive heart failure, chronic pain and chronic obstructive pulmonary disease as assessed by medical history and medical record review.
-
Patients with schizophrenia, primary anxiety disorder and active substance abuse as determined by SCID.
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Patients on or with history of failure or intolerance to respond to quetiapine.
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Patient with positive Alcohol Use Disorders Identification Test (AUDIT) with a total score above 8.
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Patients with dementia brain degenerative diseases, cognitive disorders and Mini Mental Status Examination (MMSE) score of less or equal to 24.
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Patients who are in an acute depressive, manic, hypomanic or mixed state as reflected by SCID
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Patients on concurrent sedating medications that would confound interpretation of the results. This is operationalized as follow: Sedating medications must be present and stable dosage for at least 14 days prior to enrollment in the study. If the medication is not prescribed as a primary sleep aid, it will be continued. Our rationale is that patients may need these medications and the initial sedating effect will have plateaued by 14 days. However, medications prescribed to assist insomnia will be discontinued as they are not effective for the subjects who otherwise meet inclusion ad exclusion criteria for the current study. Medications will be tapered as clinically indicated after the patients sing informed consent and prior to baseline assessment.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Michael Debakey VAMC | Houston | Texas | United States | 77030 |
Sponsors and Collaborators
- Michael E. DeBakey VA Medical Center
Investigators
- Principal Investigator: Rayan k Al Jurdi, Michael Debakey VAMC, Baylor College of Medicine
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- H-19343