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Recruiting NCT07654205

NCT07654205 Smartphone-based Intervention for Young Adults With ADHD

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Clinical Trial Summary
NCT ID NCT07654205
Status Recruiting
Phase
Sponsor Traci Kennedy
Condition Attention Deficit/Hyperactivity Disorder(ADHD)
Study Type INTERVENTIONAL
Enrollment 70 participants
Start Date 2026-07
Primary Completion 2027-03-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 25 Years
Study Type INTERVENTIONAL
Interventions
Ecological Momentary Assessment for ADHD and Substance Use - Intervention GroupEcological Momentary Assessment for ADHD & Substance Use - Control Group

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 70 participants in total. It began in 2026-07 with a primary completion date of 2027-03-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

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 * Alcohol use disorder-severe

Contact & Investigator

Central Contact

Traci Kennedy, PhD

✉ kennedytm2@upmc.edu

📞 4122466087

Principal Investigator

Traci Kennedy, PhD.

PRINCIPAL INVESTIGATOR

University of Pittsburgh

Frequently Asked Questions

Who can join the NCT07654205 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 25 Years, studying Attention Deficit/Hyperactivity Disorder(ADHD). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07654205 currently recruiting?

Yes, NCT07654205 is actively recruiting participants. Contact the research team at kennedytm2@upmc.edu for enrollment information.

Where is the NCT07654205 trial being conducted?

This trial is being conducted at Pittsburgh, United States.

Who is sponsoring the NCT07654205 clinical trial?

NCT07654205 is sponsored by Traci Kennedy. The principal investigator is Traci Kennedy, PhD. at University of Pittsburgh. The trial plans to enroll 70 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology