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Clinical Trials/NCT00455663
NCT00455663
Completed
Not Applicable

Medication Adherence and Outcomes in Schizophrenia

The University of Texas Health Science Center at San Antonio1 site in 1 country105 target enrollmentNovember 2000
ConditionsSchizophrenia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Schizophrenia
Sponsor
The University of Texas Health Science Center at San Antonio
Enrollment
105
Locations
1
Primary Endpoint
Social and Occupational Functioning Scale Score
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

This study will compare the effectiveness of three treatments in improving medication adherence, symptoms, and function in people with schizophrenia.

Detailed Description

Schizophrenia is a chronic and severely disabling mental disorder. People with schizophrenia may experience hallucinations, delusions, disordered thinking, movement disorders, social withdrawal, and cognitive deficits. Antipsychotic medications have been effective in alleviating many of the symptoms of schizophrenia and improving the lives of people with the disease. It is well established, however, that poor adherence to antipsychotic medications can lead to relapse and rehospitalization. Cognitive deficits often contribute to treatment nonadherence by compromising patients' capacity to establish routines for taking medication. Cognitive adaptation training (CAT) is a treatment approach designed to alter the physical environment of individuals with schizophrenia to compensate for cognitive deficits and improve adaptive function. For example, various environmental supports, such as signs, checklists, and electronic devices, are used to remind patients to take their medication. Studies have shown that CAT's support system led to better treatment outcomes than those produced by standard care in people with schizophrenia. This study will compare the effectiveness of two CAT treatments versus standard treatment in improving medication adherence, symptoms, and function in people with schizophrenia. After providing a blood sample, participants in this single-blind study will be randomly assigned to Full-CAT, Pharm-CAT, or treatment as usual for 9 months. Participants receiving treatment as usual will not receive CAT support. Full-CAT will entail a comprehensive use of environmental supports to improve multiple areas of adaptive functioning. Pharm-CAT will provide support for medication adherence only. Participants assigned to one of the two CAT groups will receive weekly treatments in their homes. All participants will report to the study site once every 3 months to assess medication adherence, symptomatology, and adaptive functioning. Participants will be interviewed by the study physician for 2 to 3 hours at each visit. A member of the study staff will also visit each participant's home at a random, unannounced time once every 3 months to obtain a blood sample. Follow-up visits will occur 3 and 6 months following the end of treatment.

Registry
clinicaltrials.gov
Start Date
November 2000
End Date
January 2006
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dawn Velligan

Professor, Psychiatry

The University of Texas Health Science Center at San Antonio

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of schizophrenia or schizoaffective disorder
  • If entering the study as an inpatient, hospitalization was recent
  • Currently receiving treatment with an atypical antipsychotic and continuation on the medication has been recommended
  • Assumes primary responsibility for taking medication
  • Currently living in a stable environment

Exclusion Criteria

  • History of significant head trauma, seizure disorder, or mental retardation
  • History of alcohol or drug abuse or dependence within 1 month prior to study entry
  • History of violence within 6 months prior to study entry

Outcomes

Primary Outcomes

Social and Occupational Functioning Scale Score

Time Frame: 1 endpoint ls means combining 9 months of treatment and 6 months follow up

Scores range from 0 to 100 with higher scores reflecting better functioning. 1 Final score for endpoint created by averaging scores for 9 months of treatment and 6 months of follow up.

Medication Adherence-pill Count

Time Frame: 1 final score combined for endpoint for 9 months of treatment and 6 months follow up

% medication taken as determined by unannounced pill counts conducted in the home on 2 occasions in each 3 month period. 1 Final score for endpoint created by averaging scores for 9 months of treatment and 6 months of follow up.

Positive Symptoms

Time Frame: 1 final endpoint least sq mean combining 9 months of treatment 6 months of follow up

Positive symptoms subscale of the Brief Psychiatric Rating Scale includes delusions, hallucinations, conceptual disorganization and suspiciousness-Mean score averaging these items, variability 1-7. Higher scores reflect higher level of symptoms. 1 Final score for endpoint created by averaging scores for 9 months of treatment and 6 months of follow up.

Number of Patients Surviving Without Relapse/Exacerbation

Time Frame: 9 months of treatment 6 months follow up

A relapse was scored (only for patients meeting criteria for remission) if scores on any of the 4 items assessing positive symptoms on the Brief Psychiatric Rating Scale increased a minimum of 2 points to a score of 5 or higher, if the patient was suicidal, if the patient was hospitalized, or if the patient was unable to care for themselves without continual supervision

Study Sites (1)

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