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RUPP PI PDD: Drug and Behavioral Therapy for Children with Pervasive Developmental Disorders - Article


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Pervasive Developmental Disorders

PDD; Pervasive Development Disorder




Clinical Trial: RUPP PI PDD: Drug and Behavioral Therapy for Children with Pervasive Developmental Disorders

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 compare the safety and effectiveness of medication treatment alone to medication treatment in combination with a structured parent management training program for children with pervasive developmental disorders (PDDs).

Condition Treatment or Intervention
Child Development Disorders, Pervasive
Autistic Disorder
Asperger Syndrome
 Drug: Risperidone
 Behavior: Behavior Therapy
 Drug: Aripriprizole

MedlinePlus related topics:  Asperger's Syndrome;   Autism;   Mental Health

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

Official Title: Risperidone and Behavioral Therapy in Treatment of Children and Adolescents with Autistic Disorder

Further Study Details: 

Expected Total Enrollment:  120

Study start: February 2004;  Expected completion: September 2007
Data entry closure: July 2007

PDD can be a profoundly disabling condition across social, emotional, and academic domains. Safe and effective treatments for PDD are needed.

Participants are randomly assigned to receive either risperidone plus parent management training or risperidone alone for 24 weeks. Participants who show deterioration at Week 4 will be offered an alternative mediation treatment, aripriprizole. These participants will remain in their original treatment group (either med alone or med plus parent management training). After 6 months of treatment (Week 24), participants who respond to their treatment will be gradually discontinued from their medication treatment to learn if the response can be sustained without continued medication treatment. Adaptive and behavioral outcomes are assessed during the study and at a 1 year follow-up visit.

Eligibility

Ages Eligible for Study:  4 Years   -   13 Years,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

  • Autistic Disorder, Asperger's Disorder, or Pervasive Developmental Disorder not otherwise specified
  • Weight > 30 lbs
  • IQ >= 35 or mental age of at least 18 months

Exclusion Criteria:

  • Psychotic Disorder
  • History of intolerance or nonresponse to risperidone
  • Pregnancy
  • History of neuroleptic malignant syndrome

Location and Contact Information


Connecticut
      Yale University, New Haven,  Connecticut,  06520,  United States; Recruiting
Allison Lancor  203-785-6669    allison.lancor@yale.edu 
Larry Scahill, PhD,  Principal Investigator

Indiana
      Indiana University, Indianapolis,  Indiana,  46202,  United States; Not yet recruiting
Arlene Kohn  317-274-8162    aekohn@iupui.edu 
Marianna Zaphiriou  317-278-6253    mzaphiri@iupui.edu 
Christopher McDougle, MD,  Principal Investigator

Ohio
      Ohio State University, Columbus,  Ohio,  43210,  United States; Recruiting
Kristy Hall  614-292-3698    hall.941@osu.edu 
Lorelei Ark  614-292-7022    ark.7@osu.edu 
Michael Aman, PhD,  Principal Investigator
Eugene Arnold, MD,  Sub-Investigator

More Information

Publications

McCracken JT, McGough J, Shah B, Cronin P, Hong D, Aman MG, Arnold LE, Lindsay R, Nash P, Hollway J, McDougle CJ, Posey D, Swiezy N, Kohn A, Scahill L, Martin A, Koenig K, Volkmar F, Carroll D, Lancor A, Tierney E, Ghuman J, Gonzalez NM, Grados M, Vitiello B, Ritz L, Davies M, Robinson J, McMahon D. Risperidone in children with autism and serious behavioral problems. N Engl J Med. 2002 Aug 1;347(5):314-21.

Scahill L, McCracken J, McDougle CJ, Aman M, Arnold LE, Tierney E, Cronin P, Davies M, Ghuman J, Gonzalez N, Koenig K, Lindsay R, Martin A, McGough J, Posey DJ, Swiezy N, Volkmar F, Ritz L, Vitiello B. Methodological issues in designing a multisite trial of risperidone in children and adolescents with autism. J Child Adolesc Psychopharmacol. 2001 Winter;11(4):377-88.

McDougle CJ, Scahill L, McCracken JT, Aman MG, Tierney E, Arnold LE, Freeman BJ, Martin A, McGough JJ, Cronin P, Posey DJ, Riddle MA, Ritz L, Swiezy NB, Vitiello B, Volkmar FR, Votolato NA, Walson P. Research Units on Pediatric Psychopharmacology (RUPP) Autism Network. Background and rationale for an initial controlled study of risperidone. Child Adolesc Psychiatr Clin N Am. 2000 Jan;9(1):201-24. Review.

Study ID Numbers:  U10 MH66764; U10 MH66766; U10 MH66768
Record last reviewed:  November 2004
Last Updated:  November 9, 2004
Record first received:  March 24, 2004
ClinicalTrials.gov Identifier:  NCT00080145
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 5, 2008



Page Updated: September 6, 2005
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