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Combined Behavioral/Pharmacological Therapy for Insomnia

Primary Purpose

Sleep Initiation and Maintenance Disorders

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Cognitive-Behavioral Therapy for Insomnia
zolpidem tartrate (Ambien)
Placebo
Sponsored by
Duke University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sleep Initiation and Maintenance Disorders focused on measuring Sleep Deprivation, Insomnia, Sleep Disorders

Eligibility Criteria

21 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: be between 21 and 75 years of age have a mean total nocturnal wake time of > 60 min./night have a history of insomnia > 6 months have a history of one or more poor sleep hygiene practices such as taking 3 or more naps/week, varying bed times or wake times by > 2 hrs. from day to day, or routinely lying in bed awake for periods > 30 min Exclusion Criteria: pregnant women the terminally ill individuals with other medical conditions (e.g. chronic pain disorders, etc.) that compromise sleep individuals with major psychiatric diagnoses persons with hypnotic-dependent insomnia subjects on antidepressants or anxiolytics subjects with evidence of sleep apnea

Sites / Locations

  • Duke Sleep Disorders Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Placebo Comparator

Active Comparator

Arm Label

Cognitive Behavioral Therapy and Ambien

Cognitive Behavioral Therapy and Placebo

Cognitive Behavioral Therapy alone (no drug)

Arm Description

Cognitive Behavioral Therapy and Ambien

Cognitive Behavioral Therapy and Placebo

Cognitive Behavioral Therapy alone (no drug)

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
September 3, 2002
Last Updated
September 12, 2013
Sponsor
Duke University
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT00044629
Brief Title
Combined Behavioral/Pharmacological Therapy for Insomnia
Official Title
Combined Behavioral/Pharmacological Therapy for Insomnia
Study Type
Interventional

2. Study Status

Record Verification Date
September 2013
Overall Recruitment Status
Completed
Study Start Date
September 2001 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2006 (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duke University
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

5. Study Description

Brief Summary
This study will determine how sleeping pills can be combined with nondrug treatments to maximize the benefits of therapy for insomnia.
Detailed Description
Long-term insomnia is a common and significant health problem. Two main treatments, pharmacotherapy and behavioral therapy, have been used to help people with insomnia. Because both treatments have advantages and disadvantages, a combination of these treatments may be a good way to treat insomnia. During the first 2 weeks of the study, participants keep a sleep log, wear an actigraph (a device that resembles a wristwatch and records activity to help determine when participants are asleep or awake), and complete questionnaires. Participants are then randomly assigned to receive 6 weeks of behavioral therapy plus zolpidem tartrate (Ambien), behavioral therapy plus placebo, or behavioral therapy alone. During treatment, participants return to the clinic once a week to turn in their sleep logs, download their actigraph, and complete questionnaires. After 6 weeks, participants enter the post-treatment phase of the study, which lasts 2 weeks and is identical to the 2-week assessment at the beginning of the study. After the post-treatment phase, participants enter the follow-up period and are contacted at 3 months, 6 months, and 1 year to complete another 2-week assessment with sleep logs, actigraphy, and questionnaires.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Initiation and Maintenance Disorders
Keywords
Sleep Deprivation, Insomnia, Sleep Disorders

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
162 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cognitive Behavioral Therapy and Ambien
Arm Type
Experimental
Arm Description
Cognitive Behavioral Therapy and Ambien
Arm Title
Cognitive Behavioral Therapy and Placebo
Arm Type
Placebo Comparator
Arm Description
Cognitive Behavioral Therapy and Placebo
Arm Title
Cognitive Behavioral Therapy alone (no drug)
Arm Type
Active Comparator
Arm Description
Cognitive Behavioral Therapy alone (no drug)
Intervention Type
Behavioral
Intervention Name(s)
Cognitive-Behavioral Therapy for Insomnia
Intervention Type
Drug
Intervention Name(s)
zolpidem tartrate (Ambien)
Intervention Type
Drug
Intervention Name(s)
Placebo

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: be between 21 and 75 years of age have a mean total nocturnal wake time of > 60 min./night have a history of insomnia > 6 months have a history of one or more poor sleep hygiene practices such as taking 3 or more naps/week, varying bed times or wake times by > 2 hrs. from day to day, or routinely lying in bed awake for periods > 30 min Exclusion Criteria: pregnant women the terminally ill individuals with other medical conditions (e.g. chronic pain disorders, etc.) that compromise sleep individuals with major psychiatric diagnoses persons with hypnotic-dependent insomnia subjects on antidepressants or anxiolytics subjects with evidence of sleep apnea
Facility Information:
Facility Name
Duke Sleep Disorders Center
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Combined Behavioral/Pharmacological Therapy for Insomnia

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