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Methylphenidate vs. Risperidone for the Treatment of Children and Adolescents With ADHD and Disruptive Disorders

Primary Purpose

Attention Deficit/Hyperactivity Disorder, Oppositional Defiant Disorder, Conduct Disorder

Status
Terminated
Phase
Phase 4
Locations
Israel
Study Type
Interventional
Intervention
Methylphenidate
Risperidone
Sponsored by
Sheba Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Attention Deficit/Hyperactivity Disorder focused on measuring ADHA, ODD, Conduct disorder, Aggression, Treatment, Methylphenidate, Risperidone

Eligibility Criteria

5 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Clinical diagnosis of ADHD (any sub-type) with oppositional defiant disorder.
  • Clinical diagnosis of ADHD (any sub-type) with conduct disorder.
  • Clinical diagnosis of other specified ADHD with oppositional defiant disorder.
  • Clinical diagnosis of other specified ADHD with conduct disorder.
  • Clinical diagnosis of unspecified ADHD with oppositional defiant disorder.
  • Clinical diagnosis of unspecified ADHD with conduct disorder.

Exclusion Criteria:

  • Participant who do not qualify for inclusion criteria.
  • Participant who are not willing to join the study.
  • Epilepsy.
  • Neuro-genetic syndromes.
  • Brain tumors.
  • Autism.
  • Participants who are under psychiatric medication and have changed it (dose or kind) in the last month.
  • Congenital heart, kidney of liver defects.
  • Cardiomyopathies.
  • Past hypersensitivity to Methylphenidate or Risperidone.

Sites / Locations

  • Sheba medical center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Methylphenidate

Risperidone

Arm Description

Participants in this arm will be given either "Concerta" - a long acting (12 hours) Methylphenidate pill - once daily, in the morning (starting dose 1 mg/kg, max dose 2 mg/kg), or "Ritalin LA" - a long acting (10 hours) Methylphenidate pill - once daily, in the morning (starting dose 0.6 mg/kg, max dose 1.5 mg/kg) for children who can not swallow pills.

Participants in this arm will be given a low dose of Risperidone. Starting dose will be 0.5 mg/d, max dose will be 2 mg/d.

Outcomes

Primary Outcome Measures

Change from baseline of aggressive behaviors.
The Retrospective Modified Overt Aggression Scale (R-MOAS) will be used for the the assessment of aggressive behaviors and their response to treatment.

Secondary Outcome Measures

Clinical Global Impression - Improvement scale (CGI-I) questionnaire
The Clinical Global Impression - Improvement scale (CGI-I) is a scale used for the assessment of overall symptom change.
ADHD-RS questionnaire
The ADHD Rating Scale (ADHD-RS) is a routinely use questionnaire used for the assessment of ADHD symptomatology and it's response to treatment.
Children's Depression Rating Scale (CDRS) questionnaire
The Children's Depression Rating Scale (CDRS) is a routinely use questionnaire used for the assessment of depression symptomatology and it's response to treatment.
Young Mania Rating Scale (YMRS) questionnaire
The Young Mania Rating Scale (YMRS) is a routinely use questionnaire used for the assessment of mania symptomatology and it's response to treatment.
Children Sleep Habits Questionnaire (CSHQ)
The Children Sleep Habits Questionnaire (CSHQ) is a routinely use questionnaire used for the assessment of children sleep habits.
Clinical Global Impression - Severity (CGI-S) questionnaire
The Clinical Global Impression - Severity scale (CGI-S) is a scale used for the assessment of overall symptom severity.

Full Information

First Posted
February 11, 2014
Last Updated
March 17, 2020
Sponsor
Sheba Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT02063945
Brief Title
Methylphenidate vs. Risperidone for the Treatment of Children and Adolescents With ADHD and Disruptive Disorders
Official Title
The Assessment of Efficacy and Tolerability of Methylphenidate vs. Risperidone in the Treatment of Children and Adolescents With ADHD and Disruptive Disorders
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Terminated
Why Stopped
Major difficulties recruiting participants
Study Start Date
February 1, 2017 (Actual)
Primary Completion Date
February 1, 2018 (Actual)
Study Completion Date
February 1, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sheba Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Attention Deficit/Hyperactivity Disorder (ADHD) is one the most prevalent mental disorders among children and adolescents, with a prevalence of 5% in western culture. The basics of the disorder: inattentive and hyperactive/impulsive behaviors that manifest in a variety of settings causing a dysfunction in everyday life. ADHD can be subdivided into three sub-types: predominantly inattentive, predominantly hyperactive/impulsive or combined type. Common co-morbidities of ADHD are disruptive disorders; Oppositional defiant disorder (ODD) being the major one with about half of children with the combined sub-type ADHD and about a quarter of children with the predominantly inattentive also suffering from ODD. Conduct disorder is a co-morbidity for about a quarter of children with the combined sub-type ADHD. The co-occurrence of these disorders is thought to have a negative effect on the outcome of both of them. Methylphenidate (MPH), short or long acting, is the mainstay of medical treatment for ADHD patients, it's efficacy proven in a variety of studies. It should be noted that MPH has also been proven to have a beneficial effect on children with disruptive behaviors. For children with disruptive disorders Risperidone is the mainstay of medical treatment, and has been proven in clinical trials. To the best of their knowledge, a "head to head" study comparing these two drugs for the treatment of pediatric patients with ADHD and co-morbidity of disruptive disorders was never done before. The investigators aim is to examine the efficacy and tolerability of MPH vs. Risperidone in this population. In addition, the investigators will apply DSM5's cross cutting symptom measures scales is order to further define this unique subset of patients. Disruptive mood dysregulation disorder (DMDD) is a new diagnosis in the latest version of the diagnostic and statistical manual (DSM5). It's main features: sever recurrent temper outbursts that are inconsistent with developmental level and occur on average three times a week, the outbursts occur in at least two settings and the mood between outbursts is irritable or angry. This diagnosis is in the differential diagnosis of ADHD with disruptive disorders.
Detailed Description
Secondary study aims: Comparing the efficacy and tolerability of MPH vs. Risperidone in the treatment of depressive symptoms in children and adolescents with ADHD and disruptive disorders. Comparing the efficacy and tolerability of MPH vs. Risperidone in the treatment of manic symptoms in children and adolescents with ADHD and disruptive disorders. Comparing the impact of MPH vs. Risperidone on overall every day functioning of children and adolescents with ADHD and disruptive disorder. Comparing the impact of MPH vs. Risperidone on nighttime sleep of children and adolescents with ADHD and disruptive disorder. Comparing the impact of MPH vs. Risperidone on weight and height of children and adolescents with ADHD and disruptive disorder. Assessing the overlap between the diagnosis of ADHD and disruptive disorders and DMDD. Assessing mood disorders and response to MPH vs. Risperidone treatment in children and adolescents with ADHD and disruptive disorder.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Attention Deficit/Hyperactivity Disorder, Oppositional Defiant Disorder, Conduct Disorder
Keywords
ADHA, ODD, Conduct disorder, Aggression, Treatment, Methylphenidate, Risperidone

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
5 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Methylphenidate
Arm Type
Active Comparator
Arm Description
Participants in this arm will be given either "Concerta" - a long acting (12 hours) Methylphenidate pill - once daily, in the morning (starting dose 1 mg/kg, max dose 2 mg/kg), or "Ritalin LA" - a long acting (10 hours) Methylphenidate pill - once daily, in the morning (starting dose 0.6 mg/kg, max dose 1.5 mg/kg) for children who can not swallow pills.
Arm Title
Risperidone
Arm Type
Active Comparator
Arm Description
Participants in this arm will be given a low dose of Risperidone. Starting dose will be 0.5 mg/d, max dose will be 2 mg/d.
Intervention Type
Drug
Intervention Name(s)
Methylphenidate
Other Intervention Name(s)
Ritalin, Ritalin SR, Ritalin LA, Concerta
Intervention Description
As stated in arm/group
Intervention Type
Drug
Intervention Name(s)
Risperidone
Other Intervention Name(s)
Risperdal
Intervention Description
As stated in arm/group
Primary Outcome Measure Information:
Title
Change from baseline of aggressive behaviors.
Description
The Retrospective Modified Overt Aggression Scale (R-MOAS) will be used for the the assessment of aggressive behaviors and their response to treatment.
Time Frame
baseline, 2 weeks, 4 weeks, 8 weeks.
Secondary Outcome Measure Information:
Title
Clinical Global Impression - Improvement scale (CGI-I) questionnaire
Description
The Clinical Global Impression - Improvement scale (CGI-I) is a scale used for the assessment of overall symptom change.
Time Frame
2 weeks, 4 weeks, 8 weeks.
Title
ADHD-RS questionnaire
Description
The ADHD Rating Scale (ADHD-RS) is a routinely use questionnaire used for the assessment of ADHD symptomatology and it's response to treatment.
Time Frame
baseline, 2 weeks, 4 weeks, 8 weeks.
Title
Children's Depression Rating Scale (CDRS) questionnaire
Description
The Children's Depression Rating Scale (CDRS) is a routinely use questionnaire used for the assessment of depression symptomatology and it's response to treatment.
Time Frame
baseline, 2 weeks, 4 weeks, 8 weeks.
Title
Young Mania Rating Scale (YMRS) questionnaire
Description
The Young Mania Rating Scale (YMRS) is a routinely use questionnaire used for the assessment of mania symptomatology and it's response to treatment.
Time Frame
baseline, 2 weeks, 4 weeks, 8 weeks.
Title
Children Sleep Habits Questionnaire (CSHQ)
Description
The Children Sleep Habits Questionnaire (CSHQ) is a routinely use questionnaire used for the assessment of children sleep habits.
Time Frame
baseline, 2 weeks, 4 weeks, 8 weeks.
Title
Clinical Global Impression - Severity (CGI-S) questionnaire
Description
The Clinical Global Impression - Severity scale (CGI-S) is a scale used for the assessment of overall symptom severity.
Time Frame
baseline, 2 weeks, 4 weeks, 8 weeks.
Other Pre-specified Outcome Measures:
Title
Height and Weight
Time Frame
baseline, 2 weeks, 4 weeks, 8 weeks.
Title
Blood Tests
Description
Electrolytes, liver function tests, creatinine, Prolactin, complete blood count.
Time Frame
baseline, 8 weeks.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of ADHD (any sub-type) with oppositional defiant disorder. Clinical diagnosis of ADHD (any sub-type) with conduct disorder. Clinical diagnosis of other specified ADHD with oppositional defiant disorder. Clinical diagnosis of other specified ADHD with conduct disorder. Clinical diagnosis of unspecified ADHD with oppositional defiant disorder. Clinical diagnosis of unspecified ADHD with conduct disorder. Exclusion Criteria: Participant who do not qualify for inclusion criteria. Participant who are not willing to join the study. Epilepsy. Neuro-genetic syndromes. Brain tumors. Autism. Participants who are under psychiatric medication and have changed it (dose or kind) in the last month. Congenital heart, kidney of liver defects. Cardiomyopathies. Past hypersensitivity to Methylphenidate or Risperidone.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Doron Gothelf, professor
Organizational Affiliation
Sheba Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sheba medical center
City
Tel Hashomer
Country
Israel

12. IPD Sharing Statement

Citations:
PubMed Identifier
20535081
Citation
Connor DF, Steeber J, McBurnett K. A review of attention-deficit/hyperactivity disorder complicated by symptoms of oppositional defiant disorder or conduct disorder. J Dev Behav Pediatr. 2010 Jun;31(5):427-40. doi: 10.1097/DBP.0b013e3181e121bd.
Results Reference
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PubMed Identifier
22763750
Citation
Hodgkins P, Shaw M, Coghill D, Hechtman L. Amfetamine and methylphenidate medications for attention-deficit/hyperactivity disorder: complementary treatment options. Eur Child Adolesc Psychiatry. 2012 Sep;21(9):477-92. doi: 10.1007/s00787-012-0286-5. Epub 2012 Jul 5.
Results Reference
background
PubMed Identifier
22003063
Citation
Subcommittee on Attention-Deficit/Hyperactivity Disorder; Steering Committee on Quality Improvement and Management; Wolraich M, Brown L, Brown RT, DuPaul G, Earls M, Feldman HM, Ganiats TG, Kaplanek B, Meyer B, Perrin J, Pierce K, Reiff M, Stein MT, Visser S. ADHD: clinical practice guideline for the diagnosis, evaluation, and treatment of attention-deficit/hyperactivity disorder in children and adolescents. Pediatrics. 2011 Nov;128(5):1007-22. doi: 10.1542/peds.2011-2654. Epub 2011 Oct 16.
Results Reference
background
PubMed Identifier
22351885
Citation
Seida JC, Schouten JR, Boylan K, Newton AS, Mousavi SS, Beaith A, Vandermeer B, Dryden DM, Carrey N. Antipsychotics for children and young adults: a comparative effectiveness review. Pediatrics. 2012 Mar;129(3):e771-84. doi: 10.1542/peds.2011-2158. Epub 2012 Feb 20.
Results Reference
background
PubMed Identifier
492809
Citation
Poznanski EO, Cook SC, Carroll BJ. A depression rating scale for children. Pediatrics. 1979 Oct;64(4):442-50.
Results Reference
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PubMed Identifier
12402575
Citation
Youngstrom EA, Danielson CK, Findling RL, Gracious BL, Calabrese JR. Factor structure of the Young Mania Rating Scale for use with youths ages 5 to 17 years. J Clin Child Adolesc Psychol. 2002 Dec;31(4):567-72. doi: 10.1207/S15374424JCCP3104_15.
Results Reference
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PubMed Identifier
11145319
Citation
Owens JA, Spirito A, McGuinn M. The Children's Sleep Habits Questionnaire (CSHQ): psychometric properties of a survey instrument for school-aged children. Sleep. 2000 Dec 15;23(8):1043-51.
Results Reference
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Citation
Harris S, Oakly C, Picchioni M. Quantifying Violence in Mental Health Research. Aggression and Violent Behavior 18(6):695-701, 2013.
Results Reference
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PubMed Identifier
17450046
Citation
Armenteros JL, Lewis JE, Davalos M. Risperidone augmentation for treatment-resistant aggression in attention-deficit/hyperactivity disorder: a placebo-controlled pilot study. J Am Acad Child Adolesc Psychiatry. 2007 May;46(5):558-565. doi: 10.1097/chi.0b013e3180323354.
Results Reference
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Methylphenidate vs. Risperidone for the Treatment of Children and Adolescents With ADHD and Disruptive Disorders

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