search
Back to results

Examining Tolerance to CNS Stimulants in ADHD

Primary Purpose

Attention-deficit/Hyperactivity Disorder

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Methylphenidate
Sponsored by
Florida International University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Attention-deficit/Hyperactivity Disorder focused on measuring Tolerance to stimulant medication

Eligibility Criteria

6 Years - 12 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of attention-deficit/hyperactivity disorder
  • Full Scale IQ above 80

Exclusion Criteria:

  • Psychotropic medications for conditions other than ADHD
  • Active medical or psychiatric conditions that could be worsened by stimulants
  • Diagnosis of Autism or Asperger's Disorder
  • Documented intolerance fo methylphenidate or failed trial of OROS MPH

Sites / Locations

  • Florida International University Center for Children and Families

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Methylphenidate 7-day dosing

Methylphenidate 5-day dosing

Arm Description

During the school year, children in this arm will receive 7-day dosing of medication.

During the school year phase, these children will receive 5-day dosing with weekend holidays.

Outcomes

Primary Outcome Measures

Number of Dose Changes Required Per Protocol
Monthly evaluations of medication efficacy will be used to determine whether dose adjustments are needed due to anticipated tolerance effects.

Secondary Outcome Measures

Time to First Dose Increase
The amount of time elapsed before a child requires a dose increase during the school year will be measured in months.
Endpoint Medication Dose
Dose of medication reported in mg/kg/day

Full Information

First Posted
March 7, 2013
Last Updated
May 29, 2020
Sponsor
Florida International University
search

1. Study Identification

Unique Protocol Identification Number
NCT02039908
Brief Title
Examining Tolerance to CNS Stimulants in ADHD
Official Title
Examining Tolerance to CNS Stimulants in ADHD
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
April 2013 (undefined)
Primary Completion Date
May 2018 (Actual)
Study Completion Date
March 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Florida International University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Although stimulant medication is a well-established treatment for ADHD, it is often necessary for doctors to increase the dose over time to maintain the benefits of the medication. While medication can be very effective for improving symptoms of ADHD during the first year of use, it has not been found to significantly improve the long term course of children with ADHD. For example, in large research studies, groups of children who take medication for ten years do not have consistently better academic grades than groups of children who never used medication (individual results will vary from child to child). In order to help children with ADHD achieve the best possible outcomes, it is important for doctors to study why this happens. One possible reason is development of tolerance to the medication. Tolerance means that a drug's effects decrease when it is taken consistently over time, so that an increased dose is needed to continue showing effects. Some doctors believe that children who take stimulant medication for ADHD develop tolerance to it which would explain why benefits may not persist over time, but no research studies have been done to measure whether this occurs. This study aims to see if children show a tolerance effect to stimulant medication and whether that tolerance can be prevented by taking short breaks from the medication called medication holidays.
Detailed Description
This is an innovative evaluation of tolerance using an objective measure in an analog classroom. Each subject will complete the a 10-minute math test twice a day for three weeks on optimal dose or placebo, and then be crossed over to the other condition. Within-subject drug/placebo differences will be compared over the three weeks of exposure to assess tolerance in the analog setting. When school commences, 50% of the sample will be randomized to 7-day-a-week (continuous) dosing and 50% to 5-day-a- week (weekend holidays) dosing to examine the efficacy of prescribed weekend drug holidays for combatting need for dose escalations (tolerance) during the school year. Participants will be assessed monthly to detect deteriorating functioning. Using a standardized protocol, study physicians will increase dose for subjects in either arm who meet defined impairment thresholds. The difference between the two dosing conditions will inform regarding how best to deal with tolerance in clinical application.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Attention-deficit/Hyperactivity Disorder
Keywords
Tolerance to stimulant medication

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
267 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Methylphenidate 7-day dosing
Arm Type
Active Comparator
Arm Description
During the school year, children in this arm will receive 7-day dosing of medication.
Arm Title
Methylphenidate 5-day dosing
Arm Type
Active Comparator
Arm Description
During the school year phase, these children will receive 5-day dosing with weekend holidays.
Intervention Type
Drug
Intervention Name(s)
Methylphenidate
Other Intervention Name(s)
Concerta
Intervention Description
Children will receive a double-blind assessment to determine their optimal starting dose of Concerta. Doses will be adjusted over the course of the school year and inceased if tolerance to the medication is detected.
Primary Outcome Measure Information:
Title
Number of Dose Changes Required Per Protocol
Description
Monthly evaluations of medication efficacy will be used to determine whether dose adjustments are needed due to anticipated tolerance effects.
Time Frame
10 months
Secondary Outcome Measure Information:
Title
Time to First Dose Increase
Description
The amount of time elapsed before a child requires a dose increase during the school year will be measured in months.
Time Frame
10 months
Title
Endpoint Medication Dose
Description
Dose of medication reported in mg/kg/day
Time Frame
End of Phase 2 School Year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of attention-deficit/hyperactivity disorder Full Scale IQ above 80 Exclusion Criteria: Psychotropic medications for conditions other than ADHD Active medical or psychiatric conditions that could be worsened by stimulants Diagnosis of Autism or Asperger's Disorder Documented intolerance fo methylphenidate or failed trial of OROS MPH
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William E Pelham, Ph.D.
Organizational Affiliation
Florida International University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
James M Swanson, Ph.D.
Organizational Affiliation
Florida International University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Florida International University Center for Children and Families
City
Miami
State/Province
Florida
ZIP/Postal Code
33199
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
35604744
Citation
Pelham WE, Altszuler AR, Merrill BM, Raiker JS, Macphee FL, Ramos M, Gnagy EM, Greiner AR, Coles EK, Connor CM, Lonigan CJ, Burger L, Morrow AS, Zhao X, Swanson JM, Waxmonsky JG, Pelham WE. The effect of stimulant medication on the learning of academic curricula in children with ADHD: A randomized crossover study. J Consult Clin Psychol. 2022 May;90(5):367-380. doi: 10.1037/ccp0000725.
Results Reference
derived
Links:
URL
http://ccf.fiu.edu
Description
Center for Children and Families General Information

Learn more about this trial

Examining Tolerance to CNS Stimulants in ADHD

We'll reach out to this number within 24 hrs