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Clinical Trial Summary

The purpose of this study is to test the effectiveness of a telehealth-delivered skills training versus active control group for middle and high school students with ADHD symptoms. Both programs will be delivered digitally (via Zoom). Investigators will measure student functioning at baseline, post-group, and three-month follow-up. The primary outcomes are ADHD symptoms, student grade point average, and attendance as reported in the gradebook. Secondary outcomes include parent academic support, autonomy, academic motivation, and organization skills. Participant satisfaction with the group will be measured post-group. Group attendance and homework completion will also be measured.


Clinical Trial Description

120 middle and high school students with elevated ADHD symptoms will be recruited for this study, which will take place over the course of the 2021-2022 academic year. The recruitment strategy will be to distribute information about the study opportunity to educator email lists in South Florida (see appended email template). Educators will be instructed to share information about the study to the parents of students who perceive to experience ADHD symptoms in their schools, regardless of special education status or documentation of a disability. Students who enroll will be randomly assigned to either receive the STAND-G strategy-based group or a peer-support-based, active control group. Investigators will blind participants and their parents to which group is the active treatment by informing parents and students that participant will be randomly assigned to one of two groups to help improve school difficulties in youth. The two groups will be of equal duration, both will be led by the same instructors; and will differ only in content (teaching strategies vs. facilitating peer support and problem-solving conversations). Students (and their parents) will complete assessments at baseline, post-group, and three months post-group. School records will be obtained for all time points. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05386251
Study type Interventional
Source Seattle Children's Hospital
Contact Margaret Sibley, Ph.D.
Phone 206) 884-1424
Email margaret.sibley@seattlechildrens.org
Status Not yet recruiting
Phase Phase 2/Phase 3
Start date May 18, 2022
Completion date September 30, 2022

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