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The Effects of Long-acting Methylphenidate on Academic Activity and Related Constructs in Children With ADHD

Primary Purpose

Attention Deficit Hyperactivity Disorder

Status
Completed
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
Methylphenidate
Placebo
Sponsored by
VU University of Amsterdam
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, Methylphenidate, Academic, Motivation

Eligibility Criteria

8 Years - 12 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • ADHD diagnosis (DSM-IV)
  • primary school education
  • sufficient knowledge of Dutch language

Exclusion Criteria:

  • neurological or psychiatric disorder other than ODD, CD, learning disorder, dyslexia, anxiety disorder

Healthy volunteers are accepted for the control group

Sites / Locations

  • Vrije Universiteit Amsterdam

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Drug: Methylphenidate

Drug: Placebo

Arm Description

Drug: Methylphenidate 7 days dosage as (prior to study) clinically titrated long acting Equasym (brand)

Drug: Placebo 7 days Empty green-yellow capsule

Outcomes

Primary Outcome Measures

Mathematical performance
A standardized task for mathematics is used. Productivity (% completed) and accuracy (%correct) will be calculated for analysis.
Reading performance
A standardized task for technical reading ability is used. Productivity (% completed) and accuracy (%correct) will be calculated for analysis.
Spelling performance
A standardized task for spelling is used. Productivity (% completed) and accuracy (%correct) will be calculated for analysis.

Secondary Outcome Measures

Cognitive performance
Cognitive performance will be measured with standardized tasks for interference control, verbal and spatial working memory. Using principal component analysis a combined (composite) score for cognitive performance will be calculated based on correlations between the measures.
Academic motivation
Academic motivation will be measured with a questionnaire measuring intrinsic motivation for schoolwork. In addition, an academic competence questionnaire will be completed by children, parents and teachers separately. A composite score will be calculated of these measures.
Classroom behavior
Classroom behavior will be measured with observation scales (by an independent observer) and behavioral rating scales (completed by teachers). Using principal component analysis, these scales will be combined (composite scores), depending on correlations between the measures.

Full Information

First Posted
April 9, 2014
Last Updated
May 12, 2016
Sponsor
VU University of Amsterdam
Collaborators
Shire
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1. Study Identification

Unique Protocol Identification Number
NCT02501798
Brief Title
The Effects of Long-acting Methylphenidate on Academic Activity and Related Constructs in Children With ADHD
Official Title
The Effects of Long-acting Methylphenidate on Academic Activity and Related Constructs in Children With ADHD: A Randomised Placebo Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Completed
Study Start Date
January 2013 (undefined)
Primary Completion Date
July 2015 (Actual)
Study Completion Date
May 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
VU University of Amsterdam
Collaborators
Shire

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study aims at investigating the direct effects of methylphenidate on school performance of primary school children. Although behavioral effects of this frequently prescribed drug are thoroughly studied (and confirmed), the effects of methylphenidate on school performance are less clear. Recent overviews indicate that effects are mainly quantitative and subject-specific. To gain more insight in this issue, the current double blind placebo controlled crossover study investigates not only the effects of methylphenidate on school performance but also it's effect on related variables such as short term memory, motivation and behavior. 60 children with ADHD are included and tested twice (with medication and with placebo) at their primary school.
Detailed Description
Rationale: ADHD (attention deficit hyperactivity disorder) is a common childhood developmental disorder. Besides the behavioural symptoms of ADHD, many children with ADHD experience problems with academic activities. More specifically, these children show problems with math, spelling and reading. The most common treatment for ADHD is medical treatment with methylphenidate (MPH). This treatment is effective in the reduction of ADHD symptoms. However, it is unclear whether treatment with MPH can also improve academic activity. If MPH improves academic activity, it is of great interest to understand which variables influence or mediate this effect. The results from this study can give more insight in the working mechanisms and effectiveness of MPH in reducing the academic problems commonly observed in children with ADHD. Objectives: The main objective of this study is to assess the impact of MPH on academic activity and to estimate the role of three putative mediators in this relation. Study design and population: This study is a randomised, double-blind, placebo-controlled cross-over design with a patient group and a control group. Main study parameters/endpoints: The main study parameters are changes in academic activity (ability, effort and engagement). In addition, changes in putative mediators are assessed.

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, Methylphenidate, Academic, Motivation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
61 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Drug: Methylphenidate
Arm Type
Experimental
Arm Description
Drug: Methylphenidate 7 days dosage as (prior to study) clinically titrated long acting Equasym (brand)
Arm Title
Drug: Placebo
Arm Type
Active Comparator
Arm Description
Drug: Placebo 7 days Empty green-yellow capsule
Intervention Type
Drug
Intervention Name(s)
Methylphenidate
Other Intervention Name(s)
Equasym
Intervention Description
Drug: Methylphenidate
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
empty capsule
Intervention Description
Drug: Placebo
Primary Outcome Measure Information:
Title
Mathematical performance
Description
A standardized task for mathematics is used. Productivity (% completed) and accuracy (%correct) will be calculated for analysis.
Time Frame
3.5 years
Title
Reading performance
Description
A standardized task for technical reading ability is used. Productivity (% completed) and accuracy (%correct) will be calculated for analysis.
Time Frame
3.5 years
Title
Spelling performance
Description
A standardized task for spelling is used. Productivity (% completed) and accuracy (%correct) will be calculated for analysis.
Time Frame
3.5 years
Secondary Outcome Measure Information:
Title
Cognitive performance
Description
Cognitive performance will be measured with standardized tasks for interference control, verbal and spatial working memory. Using principal component analysis a combined (composite) score for cognitive performance will be calculated based on correlations between the measures.
Time Frame
3.5 years
Title
Academic motivation
Description
Academic motivation will be measured with a questionnaire measuring intrinsic motivation for schoolwork. In addition, an academic competence questionnaire will be completed by children, parents and teachers separately. A composite score will be calculated of these measures.
Time Frame
3.5 years
Title
Classroom behavior
Description
Classroom behavior will be measured with observation scales (by an independent observer) and behavioral rating scales (completed by teachers). Using principal component analysis, these scales will be combined (composite scores), depending on correlations between the measures.
Time Frame
3.5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: ADHD diagnosis (DSM-IV) primary school education sufficient knowledge of Dutch language Exclusion Criteria: neurological or psychiatric disorder other than ODD, CD, learning disorder, dyslexia, anxiety disorder Healthy volunteers are accepted for the control group
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jaap Oosterlaan, Prof. Dr.
Organizational Affiliation
VU University of Amsterdam
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vrije Universiteit Amsterdam
City
Amsterdam
ZIP/Postal Code
1081BT
Country
Netherlands

12. IPD Sharing Statement

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The Effects of Long-acting Methylphenidate on Academic Activity and Related Constructs in Children With ADHD

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