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Tools to Improve Medication Continuity in Adolescents With ADHD

Primary Purpose

Attention Deficit Hyperactivity Disorder

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Mehealth for ADHD software with medication continuity tools
Mehealth for ADHD software without medication continuity tools
Sponsored by
Children's Hospital Medical Center, Cincinnati
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Attention Deficit Hyperactivity Disorder

Eligibility Criteria

11 Years - 15 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • First prescribed ADHD medicine more than one year prior to enrollment
  • Registered on myADHDportal.com at practice participating in study
  • Filled at least one prescription for a stimulant medication in the past year

Exclusion Criteria:

  • More than 80% of days covered with medicine over past one year
  • Poor understanding level: The participant and parent cannot understand or follow instructions given in the study.

Sites / Locations

  • Cincinnati Children's Hospital Medical Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Intervention

Arm Description

All adolescent/parent dyads enrolled at each practice will have access to the meHealth for ADHD software without medication continuity tools prior to being given access to the medication continuity tools.

Outcomes

Primary Outcome Measures

Proportion of days covered with medicine
This will be calculated based pharmacy dispensing records

Secondary Outcome Measures

Fidelity to intended use of intervention components
Proportion of intervention components completed relative to the components that were recommended by the portal based on adolescent/parent responses to the assessment battery.
Change in pre-intention factors of Unified Theory of Behavior Change influencing medication continuity
Adolescent and parent self-report on a 7 point scale. Individual items measure specific attitudes, subjective norms, and perceived behavioral control. Higher scores indicate a stronger intention to perform the behavior
Change in intention to take/give ADHD medicine regularly
Adolescent and parent self-report on 7 point scale. Higher scores indicate a stronger intention.
Change in adolescent report of medication barriers
Adolescent self-report on the 17 item Adolescent Medication Barriers Scale using 5 point Likert scale. Minimum score = 17, Maximum score = 85. Higher score means more barriers.
Change in parent report of medication barriers
Parent self-report on the 16 item Parent Medication Barriers Scale using 5 point Likert scale. Minimum score = 16, Maximum score = 80. Higher score means more barriers.
Change in medication diversion
Adolescent self-report of the number of occasions of giving away, trading, or selling ADHD medicine to someone for whom it was not prescribed.
Change in Decision Making Involvement Scale
Adolescent and Parent self-report. The scale contains the following subscales: "Child Seek" (e.g. child asks for an opinion or information from the parent), "Child Express" (e.g. child expresses an opinion or information to the parent), "Parent Seek" (e.g. parent asks for an opinion or information from child), "Parent Express" (e.g. parent expresses advice, an opinion, or information to the child), and "Joint/Options" (e.g. negotiation and brainstorming between child and parent). Each subscale produces a score which ranges from 1 to 4 with higher scores indicating more of that behavior.

Full Information

First Posted
November 5, 2019
Last Updated
January 5, 2022
Sponsor
Children's Hospital Medical Center, Cincinnati
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1. Study Identification

Unique Protocol Identification Number
NCT04173000
Brief Title
Tools to Improve Medication Continuity in Adolescents With ADHD
Official Title
Web Based Tools to Improve Medication Continuity in Adolescents With ADHD
Study Type
Interventional

2. Study Status

Record Verification Date
January 2022
Overall Recruitment Status
Completed
Study Start Date
July 2, 2019 (Actual)
Primary Completion Date
February 16, 2021 (Actual)
Study Completion Date
May 24, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Children's Hospital Medical Center, Cincinnati

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Medication is an efficacious treatment strategy for adolescents with attention-deficit/hyperactivity disorder (ADHD), however use significantly declines during adolescence when the consequences of ADHD are most severe (e.g. dropping out of school, delinquency, etc.). The Unified Theory of Behavior Change (UTBC) has been proposed as a conceptual model to explain the mechanism underlying ADHD medication adherence and to guide the development of interventions to improve the continuity of treatment. The UTBC is a well-established and empirically tested model that identifies factors that influence an individual's intention to perform a behavior as well as factors that influence whether a behavior is actually carried out. Indeed, the research team's preliminary data support the relevance of pre-intention factors and implementation factors for medication continuity among adolescents with ADHD. Currently, no evidence-based interventions target medication continuity for adolescents with ADHD. The objective of this study is to test a multi-component intervention that systematically identifies and targets aspects of the UTBC model most relevant for each adolescent with poor ADHD medication continuity. The central hypothesis is that the tailored intervention will support ADHD medication continuity. The study will conduct an open label trial among adolescents with poor medication continuity to test whether the intervention engages the mechanism underlying medication continuity and improves outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Attention Deficit Hyperactivity Disorder

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Open Label Trial
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
All adolescent/parent dyads enrolled at each practice will have access to the meHealth for ADHD software without medication continuity tools prior to being given access to the medication continuity tools.
Intervention Type
Other
Intervention Name(s)
Mehealth for ADHD software with medication continuity tools
Intervention Description
Medication continuity tools integrated within the mehealth for ADHD software will assess factors influencing medication continuity for each adolescent and recommends tools to address relevant factors. Tools include 1) a system to track outcomes and resolve uncertainty about the need for and/or benefit from medicine, 2) a module to address stigma, 3) a module to help manage side effects, and 4) reminders to take medicine and/or request refills.
Intervention Type
Other
Intervention Name(s)
Mehealth for ADHD software without medication continuity tools
Intervention Description
The mehealth for ADHD software has multiple functionalities including 1) online training regarding the American Academy of Pediatrics (AAP) ADHD guidelines; 2) an ADHD workflow wizard that guides pediatricians through the creation of an efficient office workflow to deliver quality ADHD care; 3) online collection of parent- and teacher-report ADHD rating scales for the assessment of ADHD as well as monitoring response to medication treatment; 4) integrated algorithms that automatically score rating scales in real time and provide pediatricians with assessment and treatment reports as well as immediate warnings; 5) a communication feature that allows parents, teachers, and pediatricians to communicate with each other; 6) an online pediatrician "report card"; and 7) a Plan-Do-Study-Act wizard that allows pediatricians to select a practice behavior to improve based on their report card and guides them through the creation of small tests of change to improve their office systems.
Primary Outcome Measure Information:
Title
Proportion of days covered with medicine
Description
This will be calculated based pharmacy dispensing records
Time Frame
An average of 4 months
Secondary Outcome Measure Information:
Title
Fidelity to intended use of intervention components
Description
Proportion of intervention components completed relative to the components that were recommended by the portal based on adolescent/parent responses to the assessment battery.
Time Frame
An average of 4 months
Title
Change in pre-intention factors of Unified Theory of Behavior Change influencing medication continuity
Description
Adolescent and parent self-report on a 7 point scale. Individual items measure specific attitudes, subjective norms, and perceived behavioral control. Higher scores indicate a stronger intention to perform the behavior
Time Frame
At baseline and 4 months later
Title
Change in intention to take/give ADHD medicine regularly
Description
Adolescent and parent self-report on 7 point scale. Higher scores indicate a stronger intention.
Time Frame
At baseline and 4 months later
Title
Change in adolescent report of medication barriers
Description
Adolescent self-report on the 17 item Adolescent Medication Barriers Scale using 5 point Likert scale. Minimum score = 17, Maximum score = 85. Higher score means more barriers.
Time Frame
At baseline and 4 months later
Title
Change in parent report of medication barriers
Description
Parent self-report on the 16 item Parent Medication Barriers Scale using 5 point Likert scale. Minimum score = 16, Maximum score = 80. Higher score means more barriers.
Time Frame
At baseline and 4 months later
Title
Change in medication diversion
Description
Adolescent self-report of the number of occasions of giving away, trading, or selling ADHD medicine to someone for whom it was not prescribed.
Time Frame
At baseline and 4 months later
Title
Change in Decision Making Involvement Scale
Description
Adolescent and Parent self-report. The scale contains the following subscales: "Child Seek" (e.g. child asks for an opinion or information from the parent), "Child Express" (e.g. child expresses an opinion or information to the parent), "Parent Seek" (e.g. parent asks for an opinion or information from child), "Parent Express" (e.g. parent expresses advice, an opinion, or information to the child), and "Joint/Options" (e.g. negotiation and brainstorming between child and parent). Each subscale produces a score which ranges from 1 to 4 with higher scores indicating more of that behavior.
Time Frame
At baseline and 4 months later

10. Eligibility

Sex
All
Minimum Age & Unit of Time
11 Years
Maximum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: First prescribed ADHD medicine more than one year prior to enrollment Registered on myADHDportal.com at practice participating in study Filled at least one prescription for a stimulant medication in the past year Exclusion Criteria: More than 80% of days covered with medicine over past one year Poor understanding level: The participant and parent cannot understand or follow instructions given in the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William Brinkman, MD
Organizational Affiliation
Cincinnati Children's
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cincinnati Children's Hospital Medical Center
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45229-3039
Country
United States

12. IPD Sharing Statement

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Tools to Improve Medication Continuity in Adolescents With ADHD

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