Trial record 6 of 693 for:    insomnia

Behavioral Insomnia Therapy For Those With Insomnia and Depression

This study is currently recruiting participants. (see Contacts and Locations)
Verified May 2013 by Ryerson University
Sponsor:
Information provided by (Responsible Party):
Colleen Carney, Ryerson University
ClinicalTrials.gov Identifier:
NCT00620789
First received: February 12, 2008
Last updated: May 30, 2013
Last verified: May 2013
  Purpose

This study is a randomized clinical trial to test the efficacy of Cognitive-Behavioral Insomnia Therapy when used in isolation or in combination with antidepressant medication (escitalopram) among patients with Major depressive disorder and insomnia.


Condition Intervention
Insomnia
Major Depressive Disorder
Drug: Escitalopram + CBT-I
Behavioral: CBT-I plus placebo antidepressant medication
Drug: Escitalopram

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator)
Primary Purpose: Treatment
Official Title: Behavioral Insomnia Therapy For Those With Insomnia and Depression

Resource links provided by NLM:


Further study details as provided by Ryerson University:

Primary Outcome Measures:
  • Mean two-week sleep log estimate of post-treatment sleep continuity [ Time Frame: An average of two-weeks post-treatment ] [ Designated as safety issue: No ]
    Mean two-week post-treatment sleep log sleep continuity


Secondary Outcome Measures:
  • Mean two-night polysomnographic post-treatment sleep continuity [ Time Frame: An average of two-weeks post-treatment ] [ Designated as safety issue: No ]
    Mean two-night polysomnographic post-treatment sleep continuity


Estimated Enrollment: 477
Study Start Date: March 2008
Estimated Study Completion Date: January 2014
Estimated Primary Completion Date: January 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: 1
Cognitive-Behavior Therapy for insomnia (CBT-I) + Antidepressant medication
Drug: Escitalopram + CBT-I
  • Escitalopram, 10 mg daily for the duration of the study (6 months)
  • CBT-I, four biweekly sessions during eight week Treatment phase.
Other Names:
  • Escitalopram,Lexipro
  • CBT-I, Cognitive Behavioral Therapy-Insomnia
Placebo Comparator: 2
Cognitive Behavior Therapy for Insomnia (CBT-I) + placebo medication
Behavioral: CBT-I plus placebo antidepressant medication
  • CBT-I, 4 biweekly sessions, eight week Treatment phase.
  • Placebo,daily for duration of study(6 months).
Other Name: CBT-I, Cognitive Behavioral Therapy Insomnia
Sham Comparator: 3
Antidepressant medication + Sleep Hygiene Control (SH)
Drug: Escitalopram
  • Escitalopram, 10 mg daily for the duration of the study (6 months)
  • SH, four biweekly sessions during eight week Treatment phase
Other Names:
  • Escitalopram, Lexipro
  • SH,Sleep Hygiene

Detailed Description:

Major depressive disorder (MDD) is a highly prevalent and debilitating condition that reduces quality of life, increases health care utilization, markedly impairs social/occupational functioning, and enhances suicide risk for countless individuals worldwide. A substantial proportion of MDD patients present with comorbid insomnia that significantly complicates their clinical management. For many such patients, insomnia represents a longstanding and problematic condition that predates the onset of MDD, adds to their suicide risk, dampens their response to traditional depression treatment, and enhances the likelihood for MDD relapse. Moreover, many patients who show remission of depressive symptoms with traditional therapies (e.g., antidepressant medications, cognitive therapy) suffer from residual insomnia that increases their chances for eventual relapse. Despite the deleterious effects insomnia may have on MDD patients, there has been surprisingly little research to test effective insomnia management strategies among this patient group. Some reports suggest that depression treatments may benefit from adding a hypnotic medication to traditional depression therapy, but this approach has it limits since sleep improvements achieved with hypnotics do not endure after hypnotic discontinuation. Cognitive-Behavioral Insomnia Therapy (CBT-I) represents a promising alternative treatment for MDD since it is highly effective and produces sleep improvements that persist well beyond the discontinuation of acute therapy. Unfortunately CBT-I has yet to be tested among MDD patients with comorbid insomnia. In the current project, we will conduct a randomized clinical trial to test the efficacy of CBT-I when used in isolation or in combination with antidepressant medication (escitalopram) among MDD patients with comorbid insomnia. A sample of 201 patients with MDD and comorbid insomnia will be randomized to treatments consisting of the combination of antidepressant medication plus CBT-I, antidepressant medication plus placebo behavioral insomnia therapy, or CBT-I plus a placebo medication. Objective (polysomnography, actigraph) and subjective (sleep diary, questionnaires) sleep measures, as well as depression and quality of life measures will be obtained before therapy, after an 8-week treatment phase, and at 6-months follow-up. Results of this trial will provide important new information about the short and long-term management of those highly challenging and difficult to treat patients with insomnia comorbid to MDD.

Hypothesis I asserts that the combined CBT-I+AD therapy will produce significantly greater pre-to-post therapy improvements in sleep continuity measures than will the 2 mono-therapy conditions. The primary outcomes for these hypotheses are subjective (sleep diary) measures of TWT and SE. These sleep measures are recorded daily for 2-week periods at baseline, post-treatment, and the 6-month follow-up. The daily measures will be averaged over each 2-week period. As a result, patients will have three repeated outcomes for each of the two sleep measures: one representing the average at baseline, one for the average at post-treatment, and one for the average at 6-months. Sleep diary estimates of TWT and SE from pre to post treatment will serve as the primary measures to test this hypothesis. Our secondary outcome measures include diary estimates of total sleep time (TST), as well as objective measures of TWT, SE, & TST taken from pre-and post-treatment PSG and actigraphic monitoring We will use a 3 (treatment groups) x 2 (Baseline vs. post-treatment) Analysis of Variance (ANOVA) model to compare the performance of our treatment conditions across the primary and secondary outcomes. Treatment comparisons of CBT-I + AD vs. each of the other 2 treatments will be made. Alpha for the 2 primary outcomes is fixed at 0.025 (= 0.05/2). Further analyses will adjust for pre-treatment stratification variables and other covariates. The investigators will, in particular, be mindful of the treatment adherence and credibility data we collect and use these measures as covariates if the investigators find differential adherence or credibility rates across treatment conditions. In addition, the investigators will explore the effect of changes in medication on the observed changes in our outcome measures by considering medication usage data derived from the MQS106.

  Eligibility

Ages Eligible for Study:   21 Years to 64 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • aged 21-64 years old
  • insomnia complaint of at least one month duration that meets the Research Diagnostic Criteria for Insomnia
  • meet DSM-IV criteria for a Major Depressive Episode (without psychotic features) as verified by the mood module of the Structured Clinical Interview for DSM-IV Axis I Disorders (SCID

Exclusion Criteria:

  • need immediate psychiatric (e.g., imminently suicidal patients) or medical care (e.g., patients with acute cardiac symptoms), or have attempted suicide in the past 6 months
  • have a sleep-disruptive comorbid medical condition (e.g., moderate to severe rheumatoid arthritis
  • are pregnant, trying to get pregnant, or not currently practicing adequate birth control methods
  • score < 27 on the Mini-Mental Status Exam
  • meet DSM-IV criteria for Obsessive-Compulsive disorder, Generalized Anxiety Disorder, Post-Traumatic Stress Disorder, Acute Stress Disorder, Panic Disorder, Bipolar Disorder, Schizophrenia or any other psychotic disorders on the basis of a SCID interview
  • meet DSM-IV criteria for Antisocial Personality Disorder or Borderline Personality Disorder on the basis of a SCID II interview schedule
  • report frequent travel across time zones or work rotating or night shifts
  • meet criteria for sleep apnea, restless legs syndrome or Circadian Rhythm Sleep Disorder on the basis of the Duke Structured Interview of Sleep Disorders (DSISD)
  • have an apnea-hypopnea index > 15 or periodic limb movement-related arousal index > 15 per hour of sleep during a screening laboratory polysomnogram
  • have a history of alcohol, narcotic, benzodiazepine, or other substance abuse or dependence in the 6 months prior to screening or have a positive urine drug or alcohol test at the time of screening
  • report having taken the study drug (escitalopram) for 28 days or more and then discontinuing the medication due to side effects or adverse event
  • have a disorder characterized by altered metabolism, a seizure disorder, severe renal impairment, a history of upper gastrointestinal bleed disorder, or a history of a condition that could interfere with the absorption, distribution, metabolism, or excretion of escitalopram
  • participated in any other investigational drug study within 30 days prior to screening or become enrolled in another such study during the time they are enrolled in the current project
  • use of any drugs known or suspected to affect hepatic or renal clearance within 30 days prior to screening for the current project
  • are taking any medications that interact with escitalopram (e.g., Cimetidine, Lithium, Sumatriptan, Carbamazepine, or Ketoconazole) and are not willing to both taper off such medications during a time period equal to more than five half lives before entering the study and abstain from such medications throughout the study
  • are unwilling or unable to abstain from non-study prescription medications for sleep (e.g., sedative hypnotics) or depression during their time in the study
  • are known to be seropositive for Human Immunodeficiency Virus (HIV).
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00620789

Contacts
Contact: Colleen Carney, PhD. 416-979-5000 ext 2177 ccarney@ryerson.ca
Contact: Olya Shuhatovich, MPH 416-979-5000 ext 2185 olya@ryerson.ca

Locations
Canada, Ontario
Ryerson University Recruiting
Toronto, Ontario, Canada, M5B2K3
Contact: Colleen Carney, PhD    416-979-5000 ext 2177    ccarney@ryerson.ca   
Contact: Olya Shuhatovich, MPH    416-979-5000 ext 2185    olya@ryerson.ca   
Sponsors and Collaborators
Ryerson University
Investigators
Principal Investigator: Colleen Carney, PhD Licensed, North Carolina Psychology Board, Ontario Psychological Association, Association for Behavioral and Cognative Therapies, ABCT Insomnia and other Sleep Disorders Special Interest Group, Sleep Research Society, American Academy of Sleep Medicine
  More Information

Additional Information:
No publications provided

Responsible Party: Colleen Carney, PhD, Department of Psychology, Ryerson University
ClinicalTrials.gov Identifier: NCT00620789     History of Changes
Other Study ID Numbers: Pro00003416, 1R01MH076856-01A2
Study First Received: February 12, 2008
Last Updated: May 30, 2013
Health Authority: United States: Institutional Review Board

Keywords provided by Ryerson University:
Insomnia
Depression

Additional relevant MeSH terms:
Depression
Depressive Disorder
Depressive Disorder, Major
Sleep Initiation and Maintenance Disorders
Behavioral Symptoms
Mood Disorders
Mental Disorders
Sleep Disorders, Intrinsic
Dyssomnias
Sleep Disorders
Nervous System Diseases
Antidepressive Agents
Citalopram
Dexetimide
Psychotropic Drugs
Central Nervous System Agents
Therapeutic Uses
Pharmacologic Actions
Antiparkinson Agents
Anti-Dyskinesia Agents
Parasympatholytics
Autonomic Agents
Peripheral Nervous System Agents
Physiological Effects of Drugs
Muscarinic Antagonists
Cholinergic Antagonists
Cholinergic Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Antidepressive Agents, Second-Generation

ClinicalTrials.gov processed this record on July 22, 2014