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Cognitive Therapy for Negative Symptoms and Functioning

Primary Purpose

Schizophrenia, Schizoaffective Disorder

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Cognitive Therapy
Treatment as Usual
Sponsored by
University of Pennsylvania
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring Cognitive Therapy, Negative Symptoms, Functional Outcomes, Schizophrenia, Schizoaffective Disorder

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Outpatient diagnosed with schizophrenia or schizoaffective disorder Prominent negative symptoms (i.e., two global subscales rated "moderate" or higher on the Scale for the Assessment of Negative Symptoms Proficiency in English Able to give informed consent Exclusion Criteria: Neurologic disease or damage Systematic medical illnesses that may compromise neurocognitive functioning (e.g., insulin dependent diabetes, heart disease) History of head injury or documented loss of consciousness Physical handicaps that would interfere with assessment procedures

Sites / Locations

  • Psychopathology Resarch Unit, Department of Psychiatry, University of Pennsylvania

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Experimental

Arm Label

Treatment as Usual

Cognitive Therapy

Arm Description

Outcomes

Primary Outcome Measures

Global Assessment Scale

Secondary Outcome Measures

Scale for Assessment of Negative Symptoms
Scale for Assessment of Positive Symptoms

Full Information

First Posted
July 7, 2006
Last Updated
May 2, 2012
Sponsor
University of Pennsylvania
Collaborators
National Alliance for Research on Schizophrenia and Depression
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1. Study Identification

Unique Protocol Identification Number
NCT00350883
Brief Title
Cognitive Therapy for Negative Symptoms and Functioning
Official Title
Cognitive Therapy for Negative Symptoms and Functioning
Study Type
Interventional

2. Study Status

Record Verification Date
May 2012
Overall Recruitment Status
Completed
Study Start Date
July 2006 (undefined)
Primary Completion Date
November 2011 (Actual)
Study Completion Date
November 2011 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Pennsylvania
Collaborators
National Alliance for Research on Schizophrenia and Depression

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This clinical trial tests the effectiveness of cognitive therapy (CT) to improve outcomes in outpatients diagnosed with schizophrenia or schizoaffective disorder who manifest prominent negative symptoms. It is hypothesized that patients receiving cognitive therapy will manifest lower negative symptom levels and improved engagement in constructive activity relative to patients who receive treatment-as-usual. Further, it is predicted that these differences between CT and TAU will be larger when patients are assessed 6 and 12 months after the end of treatment (18 and 24 months after study entry).
Detailed Description
This is a clinical trial to evaluate the efficacy of adjunctive cognitive behavioral therapy for negative symptoms and functioning in chronic outpatients diagnosed with schizophrenia or schizoaffective disorder. After a baseline assessment to ensure eligibility, seventy-five consenting patients will be randomly assigned to receive a year of cognitive therapy (CT) or to a treatment as usual (TAU) control condition. Measures of symptomatology (positive, negative and affective), functioning, neurocognition and negativistic beliefs will be administered to all participants during five formal assessment sessions to occur at 6-month intervals over the course of a two-year period. The first assessment session (Baseline) will occur shortly after (i.e., within a week, though typically on the same day) informed consent is given. If the participant qualifies for the study and is consents to randomization, assessments identical to the baseline in content will occur 6, 12, 18 and 24 months later. All evaluators will be blind to participant treatment condition at the time of assessment. The cognitive behavioral treatment will, in a collaborative and problem solving manner, target inaccurate or overly pessimistic expectations and thoughts about social and non-social performance. This psychosocial intervention will also target beliefs and attitudes that are related to positive symptoms which, in turn, exacerbate negative symptoms and impair functioning. We hypothesize that patients in the CT condition will have lower negative symptom levels and elevated functioning as compared to the TAU patients at the post-treatment assessment. Additionally, we expect that CT-treated patients will continue to improve over the follow-up period and, thereby, to continue to manifest lowered negative symptoms and elevated levels of functioning relative to TAU patients. While research over the past 10 years has demonstrated the efficacy of CT as an adjunct intervention in the treatment of schizophrenia, negative symptoms have not been targeted directly, nor has an emphasis been placed upon improving functional outcomes. Given that negative symptoms and functioning are particularly refractory in this population, there is a need for treatment innovation. In this vein, our previous research (Grant & Beck, 2006) established that defeatist attitudes regarding social and non-social performance are important mediators in the causal chains that link neurocognitive performance, negative symptoms, and functional outcomes in schizophrenia. The current trial, thus, aims to move therapy for schizophrenia forward by improving long-term outcomes for some of the most impaired individuals in psychiatric service.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Schizoaffective Disorder
Keywords
Cognitive Therapy, Negative Symptoms, Functional Outcomes, Schizophrenia, Schizoaffective Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
61 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment as Usual
Arm Type
Other
Arm Title
Cognitive Therapy
Arm Type
Experimental
Intervention Type
Behavioral
Intervention Name(s)
Cognitive Therapy
Other Intervention Name(s)
Cognitive Behavioral Therapy
Intervention Description
Goal-oriented talk therapy
Intervention Type
Other
Intervention Name(s)
Treatment as Usual
Other Intervention Name(s)
Standard care, Enriched care
Intervention Description
Keep getting usual care
Primary Outcome Measure Information:
Title
Global Assessment Scale
Time Frame
baseline, 6 month, 12 month, 18 month, 24 month
Secondary Outcome Measure Information:
Title
Scale for Assessment of Negative Symptoms
Time Frame
Baseline, 6M, 12M, 18M, 24M
Title
Scale for Assessment of Positive Symptoms
Time Frame
BL, 6M, 12M, 18M, 24M

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Outpatient diagnosed with schizophrenia or schizoaffective disorder Prominent negative symptoms (i.e., two global subscales rated "moderate" or higher on the Scale for the Assessment of Negative Symptoms Proficiency in English Able to give informed consent Exclusion Criteria: Neurologic disease or damage Systematic medical illnesses that may compromise neurocognitive functioning (e.g., insulin dependent diabetes, heart disease) History of head injury or documented loss of consciousness Physical handicaps that would interfere with assessment procedures
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Aaron T Beck, MD
Organizational Affiliation
University Professor, Department of Psychiatry, University of Pennsylvania
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Paul M Grant, PhD
Organizational Affiliation
Assistant Professor, Department of Psychiatry, University of Pennsylvania
Official's Role
Study Director
Facility Information:
Facility Name
Psychopathology Resarch Unit, Department of Psychiatry, University of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
15968839
Citation
Rector NA, Beck AT, Stolar N. The negative symptoms of schizophrenia: a cognitive perspective. Can J Psychiatry. 2005 Apr;50(5):247-57. doi: 10.1177/070674370505000503.
Results Reference
background
Citation
Beck AT, Rector NA, Stolar, NM, & Grant PM. Schizophrenia: Cognitive theory, research, and therapy. New York: Guilford Press
Results Reference
background
PubMed Identifier
21969420
Citation
Grant PM, Huh GA, Perivoliotis D, Stolar NM, Beck AT. Randomized trial to evaluate the efficacy of cognitive therapy for low-functioning patients with schizophrenia. Arch Gen Psychiatry. 2012 Feb;69(2):121-7. doi: 10.1001/archgenpsychiatry.2011.129. Epub 2011 Oct 3.
Results Reference
result
Links:
URL
http://www.beckinstitute.org
Description
Beck Institute for Cognitive Therapy and Research
URL
http://www.narsad.org/
Description
National Alliance of Research on Schizophrenia and Depression

Learn more about this trial

Cognitive Therapy for Negative Symptoms and Functioning

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