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Family Intervention for Mental Illness and Substance Abuse - Article


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Connective Tissue Disorders

Connective Tissue Disease; Dupuytren's Contracture; Mixed Connective Tissue Disease; PXE




Clinical Trial: Family Intervention for Mental Illness and Substance Abuse

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 establish and evaluate a new family intervention program for individuals with mental illness and substance use disorders and their families.

Condition Treatment or Intervention
Mental Disorders
Substance-Related Disorders
Psychotic Disorders
 Behavior: Family Intervention for Dual Diagnosis

MedlinePlus related topics:  Drug Abuse;   Mental Health;   Prescription Drug Abuse

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study

Official Title: Family Intervention for SMI and Substance Use Disorder

Further Study Details: 

Expected Total Enrollment:  140

Study start: April 2002;  Expected completion: September 2007

Substance use disorder (SUD) in persons with severe mental illness may worsen the course of psychiatric illness. The loss of family support for individuals with mental illness is a major contributing factor to housing instability, homelessness, and other problems. Despite progress toward integrating mental health and substance abuse services, interventions that improve the course of mental illness while helping the families of the mentally ill are not currently available. Enhancing skills for coping with mental illness may be an effective strategy for treating SUD, decreasing caregiver burden, and improving the long-term outcomes for people with mental illness.

Patients and their families are randomly assigned to either the Family Intervention for Dual Diagnosis (FIDD) program or family psychoeducation. The FIDD program lasts for up to 3 years and includes both single and multiple-family group formats. The family psychoeducation program consists of 6 weekly sessions. Routine assessments are conducted on all patients, and relatives are evaluated on a wide range of outcomes, including substance abuse, hospitalizations, psychiatric symptoms, legal problems, aggression, housing and homelessness, family burden, social support, and quality of life. To determine the effectiveness of the FIDD program, knowledge of mental illness and problem-solving skills are assessed in the families following treatment.

Eligibility

Ages Eligible for Study:  18 Years   -   65 Years,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

  • Have schizophrenia, schizoaffective disorder, or bipolar disorder
  • Have a current substance use disorder (within the past 6 months)
  • Are willing to have at least 4 hours of contact per week with family members or significant others
  • Plan to remain in the community
  • Have family members or significant others who consent to participate in the study and plan to remain in the community

Location and Contact Information

Kim T. Mueser, Ph.D.      603-271-5747    Kim.T.Mueser@dartmouth.edu

California
      Pacific Clinics El Camino, Santa Fe Springs,  California,  90670-3691,  United States; Recruiting
Roberto Zarate, Ph.D.  562-942-8256    rzarate@ucla.edu 

Massachusetts
      North Suffolk Mental Health Association, Chelsea,  Massachusetts,  02150,  United States; Recruiting
Corrine Cather, PhD   ccather@partners.org 

Study chairs or principal investigators

Kim T. Mueser, Ph.D.,  Principal Investigator,  Dartmouth Medical School   
Shirley Glynn, Ph.D.,  Principal Investigator,  University of California, Los Angeles   

More Information

Publications

Mueser KT, Fox L. A family intervention program for dual disorders. Community Ment Health J. 2002 Jun;38(3):253-70.

Study ID Numbers:  62629-01
Record last reviewed:  March 2005
Last Updated:  March 24, 2005
Record first received:  August 12, 2002
ClinicalTrials.gov Identifier:  NCT00043693
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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December 1, 2008



Page Updated: September 6, 2005
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