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Conduct Disorder clinical trials

View clinical trials related to Conduct Disorder.

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NCT ID: NCT00579267 Completed - Anxiety Disorders Clinical Trials

Reliability and Validity of the MINI International Neuropsychiatric Interview for Children and Adolescents (MINI-KID)

Start date: February 2004
Phase: N/A
Study type: Observational

The primary aims of this study are to assess: 1. The inter-rater and test-retest reliability of the MINI-KID 2. The validity of the standard MINI-KID interview in relation to the parent rated pencil/paper version (MINI-KID-P) and th longer clinician rated "Schedule for Affective Disorders and Schizophrenia for School Aged Children-Present and Lifetime Version (K-SADS-PL) and "expert opinion" (when available). Secondary aims will include evaluating the concordance between: The Children's Global Assessment Scale (a required part of the K-SADS) with the clinician-rated Sheehan Disability Scale (to be administered with the MINI-KID) as a measure of illness severity.

NCT ID: NCT00404911 Completed - Conduct Disorder Clinical Trials

Multi-Family Group Therapy for Reducing Behavioral Difficulties in Youth

Start date: October 2006
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT00399698 Completed - Bipolar Disorder Clinical Trials

Study to Determine Whether There Are Any Cognitive or Motor Effects From Taking the Medicine Risperidone.

Start date: May 1999
Phase: Phase 3
Study type: Interventional

This study was developed in order to assess the effects of risperidone (Risperdal) as compared with placebo on cognitive-motor performance (attention, memory, and hand steadiness) and body movements. We propose to study the effects of risperidone on cognitive-motor performance in children already medicated for severe conduct problems. We would also like to look at safety by assessing these children for dyskinetic movements. We already have a sizable cohort of children maintained on risperidone. Our hypotheses are as follows: 1. Risperidone will have no adverse effects on cognitive-motor performance in children who have received maintenance therapy for 4 to 20 months. 2. Children tested during placebo will show no more dyskinetic movements than during risperidone treatment (i.e., there will be no unmasking of tardive dyskinesia).

NCT ID: NCT00344474 Completed - Depression Clinical Trials

Personality-targeted Interventions for Adolescent Alcohol Misuse

Preventure
Start date: November 2003
Phase: Phase 2/Phase 3
Study type: Interventional

Personality targeted cognitive behavioural interventions have been shown to be effective in reducing alcohol and drug misuse in adult substance abusers (Conrod et al., 2000) and adolescent drinkers (Conrod et al, in press). As these interventions target personality traits linked to risk for addictive and non-addictive mental disorders, the aim of this study is to examine the extent to which this approach can prevent and/or reduce alcohol and drug misuse as well as have an impact on the onset or severity of emotional and behavioural problems in young people.

NCT ID: NCT00280228 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

Home Based Treatment for Drug Use in Early Adolescents

Start date: January 2006
Phase: Phase 2
Study type: Interventional

This study will compare two programs to see if they are helpful in preventing the use of substances in adolescents with attention deficit-hyperactivity disorder (ADHD), oppositional defiant disorder (ODD), or conduct disorder (CD). One of the programs involves working with adolescents and their parent(s) in their home. The other program involves working with adolescents and their parent(s) in an office setting.

NCT ID: NCT00266552 Completed - Conduct Disorder Clinical Trials

A Study of the Safety and Effectiveness of Risperidone Versus Placebo for the Treatment of Conduct Disorder in Children With Mild, Moderate, or Borderline Mental Retardation

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of the study is to assess the effectiveness and safety of an oral solution of risperidone (an antipsychotic medication) versus placebo in the treatment of conduct disorder in children with mild, moderate, or borderline mental retardation.

NCT ID: NCT00250705 Completed - Conduct Disorder Clinical Trials

Trial of Aripiprazole in the Treatment of CD in Adolescents

Start date: November 17, 2004
Phase: Phase 4
Study type: Interventional

The proposed study will be a 6-week open label study evaluating aripiprazole in the treatment of 12 male post-pubertal adolescents (13-17 years, Tanner Stage 4) diagnosed with conduct disorder. The initial dose depending on the weight of the patient will be as follows: < 25 kg = 1 mg/d; 25-50 kg = 2 mg/d; 50-70 kg = 5 mg/d; > 70 kg = 10 mg/d (Data on File, 2003, Bristol-Myers Squibb). For the first two weeks of the study, the dose will be flexible based on response and tolerance and thereafter will remain fixed.

NCT ID: NCT00250354 Completed - Conduct Disorder Clinical Trials

A Study of the Safety and Effectiveness of Risperidone for the Treatment of Conduct Disorder and Other Disruptive Behavior Disorders in Children Ages 5 to 12 With Mild, Moderate, or Borderline Mental Retardation

Start date: September 1997
Phase: Phase 3
Study type: Interventional

The purpose of the study is to assess the safety and effectiveness of oral risperidone (an antipsychotic medication) in the treatment of conduct disorder and other disruptive behavior disorders in children ages 5 to 12 with mild, moderate, or borderline mental retardation.

NCT ID: NCT00228046 Completed - Clinical trials for Attention Deficit Disorder With Hyperactivity

Medication Strategies for Treating Aggressive Behavior in Youth With Attention Deficit Hyperactivity Disorder

Start date: January 2004
Phase: Phase 4
Study type: Interventional

This study will assess whether adding a mood stabilizer, divalproex sodium, to stimulant treatment is more effective than stimulant treatment alone in reducing aggressive behavior among children with attention deficit hyperactivity disorder (ADHD).

NCT ID: NCT00154362 Completed - Conduct Disorder Clinical Trials

The Efficacy and Safety of Oral Oxcarbazepine 300-1200 mg/Day as Adjuvant Therapy in the Treatment of Adolescents With Impulsivity and Aggressive Behavior in Conduct Disorder This Study is Not Being Conducted in the United States.

Start date: April 2003
Phase: Phase 4
Study type: Interventional

Conduct disorder is a group of psychiatric symptoms that can include clinical characteristics of impulsivity and aggressive behavior. This study will investigate the efficacy a safety of oxcarbazepine in the treatment of adolescents with conduct disorder.