Skip to main content
Clinical Trials/NCT01550666
NCT01550666
Completed
Not Applicable

Treatment Development Targeting Severe and Persistent Negative Symptoms

The University of Texas Health Science Center at San Antonio1 site in 1 country96 target enrollmentJanuary 2011
ConditionsSchizophrenia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Schizophrenia
Sponsor
The University of Texas Health Science Center at San Antonio
Enrollment
96
Locations
1
Primary Endpoint
Changes in Negative Symptoms
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

People with schizophrenia often have problems with negative symptoms; expressing and identifying their emotions, their amount of speech, motivation and interests, feelings of purpose, social skills, and experiencing enjoyment. For this reason, new interventions are being developed to treat these problems. One new intervention is the Motivation and Engagement (MOVE) Program. The MOVE program is a new program which consists of weekly meetings for 9 months between a patient and a trainer. The weekly meetings will consist of goal setting and organization of the home to make daily tasks more manageable. During the weekly meetings the patient and trainer will discuss emotions and the trainer will help the patient identify their emotions.

The researchers hope to learn whether MOVE will help improve the problems. If it works the researchers will do a larger study comparing MOVE to other treatments that have addressed some of the problems already.

The therapist will ask you if the sessions can be audio taped to ensure that the therapist is doing a helpful job for you. They will also ask if the session can be video taped so that the tapes can be used to train other therapists learning about MOVE. The choice to do either of these is voluntary and you can continue to participate in the study if you choose not to have the session be audio and/or video taped.You will be provided a University Release document to provide that permission if you so choose.

Registry
clinicaltrials.gov
Start Date
January 2011
End Date
January 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dawn Velligan

Professor/Clinical Psychiatry

The University of Texas Health Science Center at San Antonio

Eligibility Criteria

Inclusion Criteria

  • Male or female between the 18-60 who meet DSM-IV criteria for schizophrenia confirmed by the Structured Clinical Interview Diagnosis (SCID-P version). Outpatient status.
  • Receiving treatment with antipsychotic medication
  • Clinically stable for a minimum of 5 months prior to screening (no significant changes in schizophrenia symptomatology, depressive symptoms, or community functioning, no hospitalizations, emergency visits or incarceration due to symptoms of schizophrenia or depression, no medication increases due to symptom exacerbation)
  • Has clinically meaningful negative symptoms as indicted by a score of 4 or higher on at least 2 of 6 of the following symptom domains as rated by the NSA-16; restricted affect, diminished emotional range, poverty of speech, curbing of interest, diminished sense of purpose, and diminished social drive
  • No more than moderate positive symptoms as indicated by a score of 5 or lower on BPRS-E items measuring delusions and hallucinations and no more than a 4 or higher on conceptual disorganization
  • No more than mild depression as indicated by a score of 3 or lower on the BPRS
  • No significant movement disorder as indicated by a score of 3 or lower on the ESRS-A
  • Able to provide evidence of a stable living environment (individual apartment, family home, board and care facility with no plans to move in the next year)

Exclusion Criteria

  • History of significant head trauma
  • History of a seizure disorder
  • Mental Retardation
  • Alcohol or drug abuse or dependence within the past 3 months
  • History of violence in the past one year

Outcomes

Primary Outcomes

Changes in Negative Symptoms

Time Frame: 9 months after treatment

During these times an assessor will ask questions regarding negative symptoms

Study Sites (1)

Loading locations...

Similar Trials