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Medication Adherence in Older People with Psychosis - Article


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Child Behavior Disorders

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Clinical Trial: Medication Adherence in Older People with Psychosis

This study is currently recruiting patients.

Sponsored by: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)

Purpose

The purpose of this study is to determine whether Medication Adherence Therapy (MAT) can significantly improve medication adherence and lower the risk of rehospitalization in older patients with psychosis. A secondary goal is to identify risk factors for nonadherence and determine whether MAT has benefits that extend beyond adherence and hospitalization.

Condition Treatment or Intervention
Schizophrenia
Psychotic Disorders
 Behavior: Medication Adherence Therapy
 Behavior: Friendly Support Group

MedlinePlus related topics:  Mental Health;   Schizophrenia

Study Type: Interventional
Study Design: Educational/Counseling/Training, Randomized, Double-Blind, Active Control, Parallel Assignment, Efficacy Study

Official Title: Medication Adherence in Older Psychotic People

Further Study Details: 

Expected Total Enrollment:  240

Study start: September 2002;  Expected completion: May 2007

Psychoses are among the most common and serious psychiatric disorders. Currently, the most effective treatment for psychoses involves the use of antipsychotic or neuroleptic medications. Unfortunately, pharmacologic regimens often do not achieve their goals because of poor medication adherence. Nonadherence to antipsychotic treatment is a considerable public health problem that leads to myriad clinical and economic burdens, including psychotic relapse, increased clinic and emergency room visits, and rehospitalization.

Participants in this study are randomly assigned to receive either MAT or supportive treatment for 12 weeks. MAT is given in 15 sessions and consists of motivational interviewing, education, and social skills and behavior modification. Individual MAT sessions are held in Weeks 1 and 12; small group sessions take place in Weeks 2 through 11. Three monthly booster group sessions begin in Week 16. Participants are assessed at baseline and at 3, 6, and 12 months. Medication adherence, psychopathology, quality of life, medication side effects, health beliefs, and functioning are assessed.

Eligibility

Ages Eligible for Study:  45 Years and above,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

  • DSM-IV criteria for schizophrenia or schizoaffective disorder
  • Outpatient status at the time of enrollment
  • Currently prescribed maintenance treatment with antipsychotic medication (typical or atypical, oral or depot)

Location and Contact Information

Emily Panich, BS      858-552-8585  Ext. 1272    epanich@vapop.ucsd.edu

California
      Division of Geriatric Psychiatry Center (University of California, San Diego), San Diego,  California,  92161,  United States; Recruiting
Patrick Downs  858-642-1094    pdowns@vapop.ucsd.edu 
Jonathon Lacro, PharmD,  Principal Investigator

Study chairs or principal investigators

Jonathon Lacro, Pharm.D.,  Principal Investigator,  VA San Diego Healthcare System & University of California, San Diego   

More Information

Division of Geriatric Psychiatry [University of California, San Diego]

Study ID Numbers:  62849-01A2
Record last reviewed:  April 2005
Last Updated:  April 7, 2005
Record first received:  October 29, 2003
ClinicalTrials.gov Identifier:  NCT00071604
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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Page Updated: September 6, 2005
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