The laboratory school protocol: its origin, use, and new applications

J Atten Disord. 2006 Aug;10(1):92-111. doi: 10.1177/1087054705286049.

Abstract

Objective: ADHD is the most common childhood psychiatric disorder, with impairments seen in home and academic settings. To investigate such impairments in a school-like setting, the laboratory school protocol (LSP) was developed at the University of California, Irvine.

Method: This model provides a rigorously controlled environment to examine pharmacodynamic and pharmacokinetic aspects of responses to treatment. A key principle of this methodology is to exercise tight control of the timing and context of measurements by establishing a cycle of activities repeated across each study day. In addition, the LSP approach has been extended to both younger and older populations than the typically studied school-aged group. This extension requires corresponding modifications in measures to characterize drug efficacy and to allow evaluation of ADHD symptoms in a highly standardized setting.

Results: This article provides guidelines for employing the LSP for the assessment of medication effects for both preschool and adolescent/adult populations.

Conclusion: The LSP can be modified to form either an Adult Workplace Environment or a Preschool Assessment Laboratory.

Publication types

  • Clinical Trial

MeSH terms

  • Attention Deficit Disorder with Hyperactivity / drug therapy*
  • Central Nervous System Stimulants / pharmacology*
  • Central Nervous System Stimulants / therapeutic use*
  • Child
  • Child, Preschool
  • Cognition / drug effects
  • Humans
  • Psychomotor Performance / drug effects*
  • Reaction Time / drug effects
  • School Health Services*

Substances

  • Central Nervous System Stimulants