WITHDRAWN

Adaptive Response to Intervention (RTI) for Students With ADHD

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Purpose: The primary purpose of the proposed project is to investigate the efficacy of Tier 1 and Tier 2 interventions delivered through a Response to Intervention (RTI) framework for children with attention-deficit/hyperactivity disorder (ADHD). Further, for children who do not respond to initial Tier 2 strategies, the proposed study will assess which additional course of intervention is most effective: (1) enhanced Tier 2 strategies or (2) stimulant medication. The majority of youth with ADHD are in general education settings, whether classified as special education students or not. Thus, experimentally evaluating the efficacy of well-developed and evidence-based behavioral interventions within a problem-solving framework such as RTI would significantly inform practice within school-based behavioral intervention teams. Project Activities: This study will employ a sequential multiple assignment randomized trial design (SMART). Prior to the beginning of the academic year, students will be randomly assigned to one of two conditions: (1) Business as Usual in which children receive whatever sequence of academic supports and interventions their teachers, school, and parents would typically put into place throughout the entire academic year and (2) an RTI approach to begin with Tier 1 classroom-wide management strategies with opportunities to add Tier 2 strategies for youth who do not respond to the initial Tier 1 approach.

Official Title

Adaptive Response to Intervention (RTI) for Students With ADHD

Quick Facts

Study Start:2018-05-14
Study Completion:2023-10-21
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:WITHDRAWN

Study ID

NCT03511976

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Child meets DSM-V diagnostic criteria for Attention-Deficit/Hyperactivity Disorder
  2. * Child will be entering grades 1 - 5
  1. * Child or sibling living in the same home has history of sustained successful treatment of ADHD with stimulant medication
  2. * Child currently has a special education placement involving placement in reduced ratio classroom or having a part or full-time aid due to behavior problems
  3. * Child has an IQ less than 70
  4. * Child has psychosis or a pervasive developmental disorder
  5. * Child is in a classroom that already has a study participant
  6. * Child is home-schooled

Contacts and Locations

Study Locations (Sites)

Florida International University Center for Children and Families
Miami, Florida, 33199
United States
Center for Children and Families, University at Buffalo
Buffalo, New York, 14214
United States

Collaborators and Investigators

Sponsor: Florida International University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2018-05-14
Study Completion Date2023-10-21

Study Record Updates

Study Start Date2018-05-14
Study Completion Date2023-10-21

Terms related to this study

Additional Relevant MeSH Terms

  • Attention Deficit Disorder With Hyperactivity