Aripiprazole for the Treatment of Schizophrenia With Co-Morbid Social Anxiety

Sponsor
University of Medicine and Dentistry of New Jersey (Other)
Overall Status
Completed
CT.gov ID
NCT00177008
Collaborator
Bristol-Myers Squibb (Industry)
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Study Details

Study Description

Brief Summary

This study will determine the efficacy of a medication switch to Aripiprazole for the treatment of schizophrenia or schizoaffective disorder in patients with moderate to high symptoms of social anxiety. Specifically the study will test the possibility that a medication switch to Aripiprazole reduces symptoms of social anxiety in this patient population.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

Although research has shown that social anxiety is very common among patients suffering from schizophrenia or schizoaffective disorder, it is rarely diagnosed and treated in this patient population. This study will determine the efficacy of a medication switch to Aripiprazole for the treatment of schizophrenia in patients with moderate to high symptoms of social anxiety. Specifically the study will test the possibility that a medication switch to Aripiprazole reduces symptoms of social anxiety in this patient population. In addition, the study will test the possibility that Aripiprazole significantly improves social adjustment, quality of life and level of functioning in these patients. The study may also assess the ability of Aripiprazole to reduce sexual dysfunction.

Study Design

Study Type:
Interventional
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Aripiprazole for the Treatment of Schizophrenia With Co-Morbid Social Anxiety
Study Start Date :
Mar 1, 2004
Study Completion Date :
Jan 1, 2007

Outcome Measures

Primary Outcome Measures

  1. Liebowitz Social Anxiety Scale- Change from Baseline to Final Visit []

  2. Sheehan Disability Scale- Change from Baseline to Final Visit []

  3. Lehman Quality of Life Interview- Change from Baseline to Final Visit []

Secondary Outcome Measures

  1. Instrumental Activities of Daily Living-Change from Baseline to Final Visit []

  2. Clinical Global Impression scales [CGI]and [CGI-C]- change from Baseline to Final Visit. []

  3. Ultimate game paradigm as a measure of social cohesion- Change from Baseline to Final Visit []

  4. Arizona sexual dysfunction scale- Change from Baseline to Final Visit []

  5. COSAPSQ -Change from Baseline to Final Visit []

  6. HAM-D-Change from Baseline to Final Visit []

  7. PANSS- Change from Baseline to Final Visit []

  8. CAGE -Change from Baseline to Final Visit []

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

Inclusion Criteria

  1. Patients meeting DSM IV diagnostic criteria for schizophrenia or schizoaffective disorder.

  2. Patients presenting with comorbid social anxiety symptoms of moderate to high severity are eligible for participation in the study. Only patients with LSAS scores above 30* qualify for the study.

  3. Age 18-65

  4. Gender: males or females

  5. Females: non-pregnant, not of child-bearing potential; if of child-bearing age must be on contraceptive such as pill or shot (condom alone not sufficient)

  6. Good general health

Exclusion Criteria:
  1. Patient does not meet DSM IV diagnostic criteria for schizophrenia or schizoaffective disorder

  2. Patient carries a diagnosis of dementia, degenerative CNS disorders, mental retardation, substance abuse or dependence other than nicotine dependence or alcohol abuse will be excluded from the study.

  3. Patients with acute medical conditions are not eligible.

  4. Patients allergic or otherwise intolerant or non-responsive to Aripiprazole

  5. Patient with history of suicidal, homicidal or assaultive plans or attempts in the past 6 months.

  6. Clinically significant EKG or lab abnormalities

Contacts and Locations

Locations

Site City State Country Postal Code
1 Robert Wood Johnson Medical School - Psychiatry Dept. Piscataway New Jersey United States 08854

Sponsors and Collaborators

  • University of Medicine and Dentistry of New Jersey
  • Bristol-Myers Squibb

Investigators

  • Principal Investigator: Theodore Petti, MD, MPH, Rutgers, The State University of New Jersey
  • Study Director: Robert Stern, MD, UMDNJ-RWJMS

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00177008
Other Study ID Numbers:
  • 4680
First Posted:
Sep 15, 2005
Last Update Posted:
Jan 29, 2007
Last Verified:
Jan 1, 2007

Study Results

No Results Posted as of Jan 29, 2007