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Clinical Trial Summary

To conduct an RCT to evaluate the efficacy of the system, we will recruit 60 children (ages 8-12) with ADHD who will be randomized to either immediate (n=30) or delayed (n=30) treatment (i.e., a wait-list control group). Among those randomized to immediate treatment, half will be assigned to DHI (delivered via a smartwatch and smartphone application) and half will be assigned to an active control treatment as usual (TAU) group who will receive the smartwatch with no assigned activities, applications, or interventions on the devices. The intervention period will last 16 weeks; after a participant has been in the delayed treatment group for 16 weeks and has completed the post-waiting period assessment, he or she will be assigned to either the intervention or active control group. Thus, 30 participants will complete the intervention and 30 will complete the active control, with half of the total sample also completing a wait-list period.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06456372
Study type Interventional
Source University of California, Riverside
Contact Jaime Smith
Phone 951-827-0741
Email jaime.smith@medsch.ucr.edu
Status Not yet recruiting
Phase N/A
Start date September 30, 2024
Completion date September 29, 2027

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