search
Back to results

Comparing the Efficacy of Methylphenidate, Dextroamphetamine and Placebo in Children Diagnosed With ADHD

Primary Purpose

Attention Deficit Hyperactivity Disorder

Status
Completed
Phase
Phase 4
Locations
Norway
Study Type
Interventional
Intervention
Methylphenidate
Placebo
Dextroamphetamine
Sponsored by
Ostfold Hospital Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Attention Deficit Hyperactivity Disorder focused on measuring ADHD, Children, Methylphenidate, Dextroamphetamine, Placebo, Crossover, Double Blind, Neuropsychological tests, Behavioural Questionnaires

Eligibility Criteria

9 Years - 14 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age from 9.0 to 14.0. ADHD diagnosis following assessment at a child & adolescent outpatient clinic. Clarification for stimulant treatment. Exclusion Criteria: Moderate or severe mental retardation. Psychosis. Proven brain damage. Sensory deficits and/or motor impairments that make the individual in question unsuitable for the relevant tests. Epilepsy. The child has previously been prescribed stimulant medication or is being treated with such medication. The child commutes between parents or there are other factors that substantially reduce the possibility of obtaining reliable observations from parents (The child needs to live in one place through out the whole trial since otherwise might severely influence the child's behaviour and the observations).

Sites / Locations

  • Ostfold Hospital Neuropsychiatric Unit
  • Østfold Hospital Neuropsychiatric Unit

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Methylphenidate, Dexamphetamine, Placebo

Arm Description

The 36 participants received each of the three medications for two weeks. Six different medication sequences are possible. The participants are randomly chosen for each of the six sequences in a way that allow six participants into each of the six sequences to balance the sequences.

Outcomes

Primary Outcome Measures

Change in ADHD and ODD symptoms
Parent and Teacher Questionnaire (completed monday till friday every week) Self-Report Questionnaire (completed once every week) Test Performance Questionnaire (completed by the child after each testsession)
Change in attention, motor activity and executive functioning
QB test is a computer based continuous performance test (visual attention and motor activity). Score!from Test of Everyday Attention - Childrens Edition (auditory attention). C. Golden version of Stroop Test(prosessing-speed and inhibitory control). Grooved Pegboard from the Hallstead battery (motor speed).
Change in side-effects
Side-Effects Rating Scale (R. Barkley)

Secondary Outcome Measures

Full Information

First Posted
September 28, 2010
Last Updated
October 13, 2010
Sponsor
Ostfold Hospital Trust
Collaborators
University of Oslo
search

1. Study Identification

Unique Protocol Identification Number
NCT01220440
Brief Title
Comparing the Efficacy of Methylphenidate, Dextroamphetamine and Placebo in Children Diagnosed With ADHD
Official Title
Comparing the Efficacy of Methylphenidate, Dextroamphetamine and Placebo in Children Diagnosed With ADHD
Study Type
Interventional

2. Study Status

Record Verification Date
October 2010
Overall Recruitment Status
Completed
Study Start Date
January 2006 (undefined)
Primary Completion Date
December 2008 (Actual)
Study Completion Date
December 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Ostfold Hospital Trust
Collaborators
University of Oslo

4. Oversight

5. Study Description

Brief Summary
The study compares the efficacy of methylphenidate, dextroamphetamine and placebo on neuropsychological functioning and behavioral symptoms in 36 children diagnosed with ADHD within a double-blind cross-over design over six weeks. The assessment of ADHD followed formalized guidelines and a diagnosis of ADHD was based on DSM-IV criteria. A neuropsychological testbattery and four behavioral questionnaires were selected as efficacy variables. The neuropsychological testbattery includes Qb-test (visual attention, inhibitory control, motor activity), Score (auditory attention), Stroop Test (processing speed, inhibitory control) and Grooved Pegboard (motor speed). The participants were tested once on each type of medication. The four questionnaires are: a)Side-Effects Rating Scale (completed by a parent at the end of each of the six weeks), b)Self-Report Questionnaire (completed by the child at the end of each of the six weeks), c)Parent and Teacher Questionnaire(completed by a parent and a teacher Monday till Friday through every week), Test Performance Questionnaire (completed by the child immediately after each of the three test sessions). Main hypothesis: A trial including both dextroamphetamine(Dex) and methylphenidate(Met) will provide better results than a trial including only Met. a)Met and Dex are efficient as treatment for ADHD compared to placebo, albeit Dex has moderately better effect compared to Met. b)At an individual level some of the participants will show positive response to one type of stimulants and no response, mixed response or adverse response to the other type of stimulant. c)Neuropsychological tests and behavioral questionnaires are moderately in agreement but also add unique information in the assessment of the effect of stimulants. d)Qb-test is sensitive and valid as a measure of the effect of stimulants.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Attention Deficit Hyperactivity Disorder
Keywords
ADHD, Children, Methylphenidate, Dextroamphetamine, Placebo, Crossover, Double Blind, Neuropsychological tests, Behavioural Questionnaires

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
36 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Methylphenidate, Dexamphetamine, Placebo
Arm Type
Experimental
Arm Description
The 36 participants received each of the three medications for two weeks. Six different medication sequences are possible. The participants are randomly chosen for each of the six sequences in a way that allow six participants into each of the six sequences to balance the sequences.
Intervention Type
Drug
Intervention Name(s)
Methylphenidate
Intervention Description
Methylphenidate:10mg x 3 for one week
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo: 1 pill x 2 for one week, 2 pills x 2 for one week.
Intervention Type
Drug
Intervention Name(s)
Dextroamphetamine
Intervention Description
Dextroamphetamine: 5mg x 2 for one week, 10mg x 2 for one week
Primary Outcome Measure Information:
Title
Change in ADHD and ODD symptoms
Description
Parent and Teacher Questionnaire (completed monday till friday every week) Self-Report Questionnaire (completed once every week) Test Performance Questionnaire (completed by the child after each testsession)
Time Frame
Every week for six weeks
Title
Change in attention, motor activity and executive functioning
Description
QB test is a computer based continuous performance test (visual attention and motor activity). Score!from Test of Everyday Attention - Childrens Edition (auditory attention). C. Golden version of Stroop Test(prosessing-speed and inhibitory control). Grooved Pegboard from the Hallstead battery (motor speed).
Time Frame
The neuropsychological tests are administered once on each type of medication during the six week trial
Title
Change in side-effects
Description
Side-Effects Rating Scale (R. Barkley)
Time Frame
Once every week through the six week trial

10. Eligibility

Sex
All
Minimum Age & Unit of Time
9 Years
Maximum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age from 9.0 to 14.0. ADHD diagnosis following assessment at a child & adolescent outpatient clinic. Clarification for stimulant treatment. Exclusion Criteria: Moderate or severe mental retardation. Psychosis. Proven brain damage. Sensory deficits and/or motor impairments that make the individual in question unsuitable for the relevant tests. Epilepsy. The child has previously been prescribed stimulant medication or is being treated with such medication. The child commutes between parents or there are other factors that substantially reduce the possibility of obtaining reliable observations from parents (The child needs to live in one place through out the whole trial since otherwise might severely influence the child's behaviour and the observations).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arne K. Henriksen, Phd
Organizational Affiliation
Ostfold Hospital Trust
Official's Role
Study Director
Facility Information:
Facility Name
Ostfold Hospital Neuropsychiatric Unit
City
Fredrikstad
State/Province
Ostfold
ZIP/Postal Code
1605
Country
Norway
Facility Name
Østfold Hospital Neuropsychiatric Unit
City
Fredrikstad
State/Province
Østfold
ZIP/Postal Code
1605
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
24666268
Citation
Ramtvedt BE, Aabech HS, Sundet K. Minimizing adverse events while maintaining clinical improvement in a pediatric attention-deficit/hyperactivity disorder crossover trial with dextroamphetamine and methylphenidate. J Child Adolesc Psychopharmacol. 2014 Apr;24(3):130-9. doi: 10.1089/cap.2013.0114. Epub 2014 Mar 25.
Results Reference
derived
PubMed Identifier
23659360
Citation
Ramtvedt BE, Roinas E, Aabech HS, Sundet KS. Clinical gains from including both dextroamphetamine and methylphenidate in stimulant trials. J Child Adolesc Psychopharmacol. 2013 Nov;23(9):597-604. doi: 10.1089/cap.2012.0085. Epub 2013 May 9.
Results Reference
derived

Learn more about this trial

Comparing the Efficacy of Methylphenidate, Dextroamphetamine and Placebo in Children Diagnosed With ADHD

We'll reach out to this number within 24 hrs