Improving Adherence to Oral Antipsychotic Medications in People With Schizophrenia (NCT00406718) | Clinical Trial Compass
CompletedNot Applicable
Improving Adherence to Oral Antipsychotic Medications in People With Schizophrenia
United States197 participantsStarted 2006-11
Plain-language summary
This study will determine the comparative effectiveness of two systems designed to improve medication adherence in people with schizophrenia.
Who can participate
Age range18 Years – 60 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Diagnosis of schizophrenia or schizoaffective disorder according to DSM-IV criteria, as determined on the basis of the Structured Clinical Interview for Diagnosis (SCID-P)
* Receiving treatment with an oral atypical antipsychotic medication other than clozapine (e.g., risperidone, olanzapine, quetiapine, aripiprazole, ziprasidone, or others as they are FDA approved)
* Assumes some responsibility for taking own medications
* Able to provide evidence of a stable living environment (e.g., individual apartment, family home, or board and care facility) within 3 months prior to study entry and no plans to move in the next year
* Intact visual and auditory ability as determined by a computerized screening battery
* Ability to read at the 5th grade level or higher based upon score on the Wide Range Achievement Test (WRAT)
* Able to understand and complete rating scales and neuropsychological testing
* Working telephone present in the home
Exclusion Criteria:
* History of significant head trauma, seizure disorder, or mental retardation
* Alcohol or drug abuse or dependence within 3 months prior to study entry
* Currently being treated by an assertive community treatment (ACT) team
* History of violence within 1 year prior to study entry
* Any hospitalizations within 3 months prior to study entry
What they're measuring
1
Adherence
Timeframe: Measured at Months 4, 7, and 10 months averaged across the treatment period which began 1 month after study baseline and ended at month 10 (total 9 mos of treatment)
2
Social and Occupational Functioning Assessment Scale (SOFAS) Scores
Timeframe: Measured at Months 4, 7, and 10 months averaged across the treatment period which began 1 month after study baseline and ended at month 10 (total 9 mos of treatment)
Trial details
NCT IDNCT00406718
SponsorThe University of Texas Health Science Center at San Antonio