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Smartphone-based Intervention for Young Adults With ADHD

Recruiting

Training Inhibitory Control Using Personalized Strategies (TIPS): A Randomized Controlled Feasibility Trial of a Smartphone-Based Intervention for Alcohol Use in Young Adults With ADHD

Who can join

Ages 18 to 25 · All sexes

Full eligibility criteria
Inclusion Criteria:

* Age 18-25
* Current diagnosis of Attention Deficit/Hyperactivity Disorder-Combined Type according to the Diagnostic and Statistical Manual of Mental Disorders - Fifth Edition (DSM 5)
* Drinks at least 4 (for females) / 5 (for males) alcoholic drinks in a single drinking session at least once per week
* Owns a smartphone
* Reads and understands English

Exclusion Criteria:

* Currently in high school
* Actively in treatment for Alcohol Use Disorder

About the study

The primary goal of this clinical trial is to test if a smartphone-based intervention is feasible \& acceptable among young adults with ADHD who also engage in risky drinking behaviors. A secondary aim is to test preliminary intervention efficacy. The main questions it aims to answer are:

Is the smartphone intervention feasible \& acceptable for participants (e.g., are they responding regularly, is there a low level of burden reported)?

Does the smartphone intervention improve symptom awareness, inhibitory control, and problematic alcohol use?

Participants will:

Attend a virtual baseline visit to assess ADHD, alcohol use, and other life experiences.

Complete either the TIPS smartphone intervention or a control smartphone protocol over the course of 31-days, starting the first Friday after the baseline visit.

Attend a virtual follow-up visit, where many of the same questions from the baseline visit will be asked again.

What is being tested

Sponsor: Traci Kennedy · Participants: 70 · Started: Jul 15, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07654205

Locations in the U.S.

PennsylvaniaUniversity of Pittsburgh, Pittsburgh

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.