MedTrace Logo

Leveraging Mobile Health Technology to Optimize Early Stimulant Medication Treatment: A Feasibility Pilot

NCT01990222 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 26

Last updated 2020-02-17

No results posted yet for this study

Summary

The goal of this study is to develop and test a mobile web application to optimize early stimulant medication treatment for children receiving care for Attention/Deficit Hyperactivity Disorder (ADHD) in a publicly-funded mental health clinic.

Conditions

  • Attention Deficit Disorder With Hyperactivity

Sponsors & Collaborators

Principal Investigators

  • Bonnie Zima, MD, MPH · University of California, Los Angeles

Eligibility

Min Age
5 Years
Max Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-01-31
Primary Completion
2018-10-31
Completion
2018-10-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01990222 on ClinicalTrials.gov