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Multi-Family Group Therapy for Reducing Behavioral Difficulties in Youth

This study is currently recruiting participants.
Verified by National Institute of Mental Health (NIMH), September 2008

Sponsored by: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)
ClinicalTrials.gov Identifier: NCT00404911
  Purpose

This study will examine the effectiveness of a multiple family group mental health service delivery strategy in improving mental health service use and outcome for urban, low income children of color, ages 7-11 years old with disruptive behaviors and their families.


Condition Intervention
Oppositional Defiant Disorder and Conduct Disorder
Behavioral: Multiple family group (MFG) therapy
Behavioral: Standard care control

MedlinePlus related topics:   Child Mental Health    Mental Health   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title:   Family Groups to Reduce Youth Behavioral Difficulties

Further study details as provided by National Institute of Mental Health (NIMH):

Primary Outcome Measures:
  • Youth externalizing behaviors and functioning [ Time Frame: Measured at Weeks 8 and 16 of treatment and Months 6 and 18 follow-ups ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Parenting skills [ Time Frame: Measured at Month 23 ] [ Designated as safety issue: No ]
  • Family functioning [ Time Frame: Measured at Month 23 ] [ Designated as safety issue: No ]
  • Involvement in child mental health care [ Time Frame: Measured at Month 23 ] [ Designated as safety issue: No ]
  • Service delivery process within family support [ Time Frame: Measured at Month 23 ] [ Designated as safety issue: No ]
  • Parent/child interaction [ Time Frame: Measured at Weeks 8 and 16 of treatment and Months 6 and 18 follow-ups ] [ Designated as safety issue: No ]

Estimated Enrollment:   372
Study Start Date:   October 2006
Estimated Study Completion Date:   October 2011
Estimated Primary Completion Date:   October 2011 (Final data collection date for primary outcome measure)

Arms Assigned Interventions
1: Experimental
Participants will receive multi-family group therapy
Behavioral: Multiple family group (MFG) therapy
MFG includes 16 weekly group therapy sessions for families with children who have ODD or CD. Sessions will include adult caregivers and all children over age 6. Each session will follow the same procedures, and will proceed through the following stages: creating social networks; information exchange; group discussions; individual family practice; and homework assignment.
Behavioral: Standard care control
Participants assigned to standard care will receive treatment that is traditionally offered to outpatients. Participants in the MFG program will also receive standard care.
2: Active Comparator
Participants will receive standard care
Behavioral: Standard care control
Participants assigned to standard care will receive treatment that is traditionally offered to outpatients. Participants in the MFG program will also receive standard care.

Detailed Description:

Oppositional defiant disorder (ODD) and conduct disorder (CD) are two common childhood psychiatric disorders. Children with ODD frequently have temper tantrums, argue excessively with adults, deliberately attempt to annoy or upset people, and blame others for their mistakes or behavior. Children with CD may exhibit aggression toward people and animals, destruction of property, deceitfulness, and rule breaking. The symptoms of these disorders can negatively affect children's social, family, and academic lives. Research has shown that early, comprehensive treatment leads to better treatment outcomes. Both disorders are commonly treated using parent training techniques. A multiple family group therapy setting may prove to be more engaging and beneficial than standard care for both parents and children. This study will examine the effectiveness of a multiple family group (MFG) mental health service delivery strategy in improving mental health service use and treatment outcome for urban, low income children of color with ODD or CD.

Participants in this 18-month, open-label study will be randomly assigned to either receive standard of care or participate in an MFG in addition to receiving standard of care. Participants assigned to standard of care will receive treatment that is traditionally offered to outpatients. Participants in an MFG will meet in their groups once a week for 16 weeks. Sessions will include adult caregivers and all children over age 6. Each session will follow the same procedures, and will proceed through the following stages: creating social networks; information exchange; group discussions; individual family practice; and homework assignment. Assessments of youth functioning will be held at Weeks 8 and 16 and Months 6 and 18 post-treatment.

  Eligibility
Ages Eligible for Study:   7 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes

Criteria

Inclusion Criteria:

  • Youth participants are between the ages of 7 and 11
  • Adult caregivers are available to participate in the research and intervention activities
  • Both youth and adult caregiver are English- or Spanish-speaking
  • Youth meets criteria for a primary diagnosis of oppositional defiant disorder or conduct disorder, as measured by the Disruptive Behavior Disorder Rating Scale (DBD)

Exclusion Criteria:

  • Youth has significant cognitive impairment that might interfere with understanding of program content or informed consent process
  • Youth or adult has emergency psychiatric needs that require services beyond those provided within an outpatient setting (e.g., hospitalization or specialized placement outside the home)
  • Youth who are wards of the state
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00404911

Contacts
Contact: Lydia Franco, LMSW     212-659-8729     lydia.franco@mountsinai.org    
Contact: Kara M. Dean-Assael, MSW     212-659-8729     mariakara@gmail.com    

Locations
United States, New York
Mount Sinai's Child and Adolescent Outpatient Psychiatry Clinic     Recruiting
      New York, New York, United States, 10029
      Contact: Lydia Franco, LMSW     212-659-8729     lydia.franco@mountsinai.org    
      Contact: Kara M. Dean-Assael, MSW     212-659-8729     mariakara@gmail.com    
      Principal Investigator: Mary M. McKay, PhD            

Sponsors and Collaborators

Investigators
Principal Investigator:     Mary M. McKay, PhD     Mount Sinai School of Medicine, Department of Psychiatry    
  More Information


Responsible Party:   Mt. Sinai School of Medicine- Department of Psychiatry ( Mary M. McKay, PhD )
Study ID Numbers:   R01 MH72649, DSIR CT-C
First Received:   November 28, 2006
Last Updated:   September 19, 2008
ClinicalTrials.gov Identifier:   NCT00404911
Health Authority:   United States: Federal Government

Keywords provided by National Institute of Mental Health (NIMH):
Oppositional Defiant Disorder  

Study placed in the following topic categories:
Conduct Disorder
Oppositional defiant disorder
Mental Disorders
Mental Disorders Diagnosed in Childhood
Attention Deficit and Disruptive Behavior Disorders

Additional relevant MeSH terms:
Pathologic Processes
Disease

ClinicalTrials.gov processed this record on November 19, 2008




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