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Paroxetine in the Treatment of Chronic Primary Insomnia

Primary Purpose

Primary Insomnia, Depression

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
paroxetine
Sponsored by
University of Pittsburgh
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Primary Insomnia focused on measuring primary insomnia, insomnia, depression, late life, elderly, sleep disorders

Eligibility Criteria

55 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age 55 or older Diagnosis of chronic primary insomnia Score of 8 or higher on the Pittsburgh Sleep Quality Index free of all antidepressants and benzodiazepine for two weeks Exclusion Criteria: lifetime diagnosis of any psychotic disorder,or bipolar disorder. DSM-IV diagnosis of dysthymia or generalized anxiety disorder Diagnosis of major depression within the past 6 months Alcohol or drug abuse within the past 6 months Contraindication to SSRI therapy History of seizure disorder Baseline apnea/hypopnea index score greater than 15 Hyponatremia

Sites / Locations

  • University of Pittsburgh Medical Center
  • University of Pittsubrgh Medical Center

Outcomes

Primary Outcome Measures

Paroxetine in combination with sleep hygiene therapy will produce a greater number of responders in acute treatment, compared to a placebo and sleep hygiene condition, in a randomized, double-blinded, six-week acute trial

Secondary Outcome Measures

Polysomnographic Sleep measures
Pittsburgh Sleep Quality Index and Sleep Diary
Daytime well being on the Profile of Mood States
Daytime functioning on the Sickness Impact Profile, Medical Outcomes Study (SF-36), and UKU
Stress measures: Schedule of Recent Events, Perceived Stress Scale, Impact of Life Events Scale, Ways of Coping Inventory, Multidimensional Fatigue Inventory, and Brief Symptom Inventory
Psychophysiological arousal and mood measures collected at each sleep study: the Pres-Sleep Arousal Scale, Spielman Insomnia Symptom Questionnaire, Pittsburgh Insomnia Rating Scale, and the Pre-Sleep Experience Questionnaire.
SCID
Sleep Hygiene Awareness and Practices Scale
Diagnostic Response: Clinical Global Impressions Scale

Full Information

First Posted
September 13, 2005
Last Updated
September 13, 2005
Sponsor
University of Pittsburgh
Collaborators
GlaxoSmithKline
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1. Study Identification

Unique Protocol Identification Number
NCT00178048
Brief Title
Paroxetine in the Treatment of Chronic Primary Insomnia
Official Title
Paroxetine in the Treatment of Chronic Primary Insomnia: A Double-Blind, Randomized, Placebo-Controlled Study of Efficacy Over Six Weeks
Study Type
Interventional

2. Study Status

Record Verification Date
September 2005
Overall Recruitment Status
Completed
Study Start Date
September 1998 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
December 2003 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
University of Pittsburgh
Collaborators
GlaxoSmithKline

4. Oversight

5. Study Description

Brief Summary
The goal of the study is to examine the role of paroxetine, an antidepressant medication, in the acute and continuation treatment of insomnia. Primary insomnia is a type of insomnia not directly resulting from general medical, chemical, or psychiatric conditions.
Detailed Description
The primary aim of this study is to demonstrate the role of paroxetine in the acute treatment of chronic primary insomnia. Paroxetine taken on a nightly basis in combination with sleep hygiene therapy will produce a greater number of diagnostic responders in acute treatment, compared to a placebo and sleep hygiene control condition, in a randomized, double-blinded, six-week acute treatment trial. EEG sleep, sleep quality, and daytime well-being, and daytime functioning will also show superior treatment effects during acute treatment with paroxetine plus sleep hygiene, as compared with the placebo control condition. A total of 66 patients with primary insomnia, as defined by DSM-IV criteria, will be randomized (1:1) to receive paroxetine plus sleep hygiene therapy (P+SH-a) or placebo plus sleep hygiene therapy (PL+SH-a) in weekly acute treatment sessions evolving over a six-week interval in a double-blinded, parallel group design.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Primary Insomnia, Depression
Keywords
primary insomnia, insomnia, depression, late life, elderly, sleep disorders

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Factorial Assignment
Masking
Double
Allocation
Randomized
Enrollment
66 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
paroxetine
Primary Outcome Measure Information:
Title
Paroxetine in combination with sleep hygiene therapy will produce a greater number of responders in acute treatment, compared to a placebo and sleep hygiene condition, in a randomized, double-blinded, six-week acute trial
Secondary Outcome Measure Information:
Title
Polysomnographic Sleep measures
Title
Pittsburgh Sleep Quality Index and Sleep Diary
Title
Daytime well being on the Profile of Mood States
Title
Daytime functioning on the Sickness Impact Profile, Medical Outcomes Study (SF-36), and UKU
Title
Stress measures: Schedule of Recent Events, Perceived Stress Scale, Impact of Life Events Scale, Ways of Coping Inventory, Multidimensional Fatigue Inventory, and Brief Symptom Inventory
Title
Psychophysiological arousal and mood measures collected at each sleep study: the Pres-Sleep Arousal Scale, Spielman Insomnia Symptom Questionnaire, Pittsburgh Insomnia Rating Scale, and the Pre-Sleep Experience Questionnaire.
Title
SCID
Title
Sleep Hygiene Awareness and Practices Scale
Title
Diagnostic Response: Clinical Global Impressions Scale

10. Eligibility

Sex
All
Minimum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 55 or older Diagnosis of chronic primary insomnia Score of 8 or higher on the Pittsburgh Sleep Quality Index free of all antidepressants and benzodiazepine for two weeks Exclusion Criteria: lifetime diagnosis of any psychotic disorder,or bipolar disorder. DSM-IV diagnosis of dysthymia or generalized anxiety disorder Diagnosis of major depression within the past 6 months Alcohol or drug abuse within the past 6 months Contraindication to SSRI therapy History of seizure disorder Baseline apnea/hypopnea index score greater than 15 Hyponatremia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charles F Reynolds III, M.D.
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Pittsburgh Medical Center
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
Facility Name
University of Pittsubrgh Medical Center
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States

12. IPD Sharing Statement

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Paroxetine in the Treatment of Chronic Primary Insomnia

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