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The Use of Quetiapine (Seroquel) in the Treatment of Social Phobia: Public Speaking Environment

Primary Purpose

Social Phobia

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

About this trial

This is an interventional treatment trial for Social Phobia focused on measuring social phobia, anxiety, quetiapine

Eligibility Criteria

18 Years - 25 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18-25
  • Primary DSM-IV Axis I diagnosis of social phobia, specific fear of public speaking
  • PRCS total score: 21 or greater (1 SD above population norm of 14.2)

Exclusion Criteria:

  • Current contraindications/sensitivity to quetiapine
  • Current prescription of benzodiazepine, tranquilizer, or antipsychotic medication
  • Current Psychotic episode
  • Current Manic episode
  • Current Depressive episode
  • Current drug or alcohol dependence
  • A patient with diabetes mellitus (DM) fulfilling one of the following criteria:

    • Unstable DM defined as enrollment glycosylated hemoglobin (HbA1c) 8.5%.
    • Admitted to hospital for treatment of DM or DM related illness within the past 12 weeks
    • Not under physician care for DM.
    • Physician responsible for patient's DM care has not indicated that the patient's DM is controlled.

Sites / Locations

  • University of Minnesota

Outcomes

Primary Outcome Measures

Personal Report of Confidence as a Speaker (PRCS)

Secondary Outcome Measures

Liebowitz Social Anxiety Scale (LSAS)
Brief Social Phobia Scale
Social Phobia Inventory
Fear of Negative Evaluation Scale
In session-Subjective Units of Distress
Blood Pressure and heart rate monitored within session

Full Information

First Posted
November 30, 2006
Last Updated
October 26, 2011
Sponsor
University of Minnesota
Collaborators
AstraZeneca
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1. Study Identification

Unique Protocol Identification Number
NCT00407199
Brief Title
The Use of Quetiapine (Seroquel) in the Treatment of Social Phobia: Public Speaking Environment
Official Title
The Use of Quetiapine (Seroquel) in the Treatment of Social Phobia: Effects on Cue Reactivity in Response to Virtual Reality Public Speaking Environment
Study Type
Interventional

2. Study Status

Record Verification Date
October 2011
Overall Recruitment Status
Completed
Study Start Date
December 2006 (undefined)
Primary Completion Date
September 2007 (Actual)
Study Completion Date
September 2007 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Minnesota
Collaborators
AstraZeneca

4. Oversight

5. Study Description

Brief Summary
This is a pilot study that will focus on the collection of preliminary data to determine the efficacy of quetiapine for individuals with social phobia. We hypothesize that individuals will react with less self-reported anxiety and physiological reactivity in the drug condition than in the placebo condition. If true, this would constitute a strong signal for a significant treatment effect for quetiapine in social phobia. A positive treatment effect in this study would provide rationale for further investigation of the efficacy of quetiapine for cue reactivity for individuals with social phobia. Further study would include increased sample size in order to obtain statistical power and replication of findings. We will utilize the IR formulation of quetiapine.
Detailed Description
Primary Objective: The purpose of this study is to evaluate the use of quetiapine to diminish cue reactivity to a Virtual Reality environment for individuals with Social Phobia. The following primary and secondary outcome measures will be administered to subjects during each Virtual Reality exposure in treatment and non-treatment conditions. The outcome measures have demonstrated adequate reliability and validity in the detection of clinical change for individuals with social phobia in open label studies using quetiapine (Schutters, van Megen, and Westenberg, 2005). The Personal Report of Confidence as a Speaker (PRCS; Paul, 1966) will be utilized as the primary measure to establish individual diagnosis and severity level. Pertaub and Slater (2002) demonstrated the sensitivity of the PRCS in measuring anxiety responses to virtual audiences. A total score of 21 or greater on the PRCS will be required for study inclusion (Carrigan and Levis, 1999). Carrigan and Lewis (1999) reported a mean score of 23.73 on the 30-item PRCS for individuals reporting fear of public speaking. Subjective units of distress ratings and measures of blood pressure and heart rate will be obtained within session in order to measure immediate changes in subject's cue reactivity to VRE stimuli. The outcome measures include: Primary Measure: Personal Report of Confidence as a Speaker (PRCS) Secondary Measures: Liebowitz Social Anxiety Scale (LSAS) Clinical Global Impressions-Improvement Scale (CGI) Brief Social Phobia Scale Social Phobia Inventory Fear of Negative Evaluation Scale Hamilton Rating Scale for Anxiety In session-Subjective Units of Distress Blood Pressure and heart rate monitored within session Design: A crossover, double-blind within subjects design will be used. The two conditions are placebo and drug prior to exposure to social anxiety cues in the virtual environment. Each subject will be in both conditions over the course of two visits. Each subject will be in only one condition on the first visit and will then cross-over to the other condition on the second visit. Order will be counter-balanced across subjects. The treatment phase of the study will include the two afore mentioned visits, totaling 60 minutes each. This will include the treatment and pre-post assessment

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Social Phobia
Keywords
social phobia, anxiety, quetiapine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
Double
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
quetiapine
Primary Outcome Measure Information:
Title
Personal Report of Confidence as a Speaker (PRCS)
Secondary Outcome Measure Information:
Title
Liebowitz Social Anxiety Scale (LSAS)
Title
Brief Social Phobia Scale
Title
Social Phobia Inventory
Title
Fear of Negative Evaluation Scale
Title
In session-Subjective Units of Distress
Title
Blood Pressure and heart rate monitored within session

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-25 Primary DSM-IV Axis I diagnosis of social phobia, specific fear of public speaking PRCS total score: 21 or greater (1 SD above population norm of 14.2) Exclusion Criteria: Current contraindications/sensitivity to quetiapine Current prescription of benzodiazepine, tranquilizer, or antipsychotic medication Current Psychotic episode Current Manic episode Current Depressive episode Current drug or alcohol dependence A patient with diabetes mellitus (DM) fulfilling one of the following criteria: Unstable DM defined as enrollment glycosylated hemoglobin (HbA1c) 8.5%. Admitted to hospital for treatment of DM or DM related illness within the past 12 weeks Not under physician care for DM. Physician responsible for patient's DM care has not indicated that the patient's DM is controlled.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David E Adson, M.D.
Organizational Affiliation
University of Minnesota
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Christopher B Donahue, Ph.D.
Organizational Affiliation
Univeristy of Minnesota
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Matt Kushner, Ph.D. LP
Organizational Affiliation
University of Minnesota
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Minnesota
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55454
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
19157776
Citation
Donahue CB, Kushner MG, Thuras PD, Murphy TG, Van Demark JB, Adson DE. Effect of quetiapine vs. placebo on response to two virtual public speaking exposures in individuals with social phobia. J Anxiety Disord. 2009 Apr;23(3):362-8. doi: 10.1016/j.janxdis.2008.12.004. Epub 2008 Dec 24.
Results Reference
result

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The Use of Quetiapine (Seroquel) in the Treatment of Social Phobia: Public Speaking Environment

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