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Behavioural Intervention

SMS Intervention for ADHD

Waitlist Available
Research Sponsored by Massachusetts General Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Screening 3 weeks
Treatment Varies
Follow Up 9 months
Awards & highlights


This trial will test whether twice-daily text messages can improve adherence to stimulants in adults with ADHD.

Eligible Conditions
  • Attention Deficit Hyperactivity Disorder (ADHD)


Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~9 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 9 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Adherence to Stimulants

Trial Design

1Treatment groups
Experimental Treatment
Group I: SMS InterventionExperimental Treatment1 Intervention
All subjects will receive customized text messages twice a day, every day for 9 months that will include reminders to adhere to the individualized medication regimen, reminders to call their clinician for a prescription refill followed by reminders to pick up medication from the pharmacy, and educational reminders about ADHD and its treatment.

Find a Location

Who is running the clinical trial?

Massachusetts General HospitalLead Sponsor
2,955 Previous Clinical Trials
13,212,561 Total Patients Enrolled
59 Trials studying Attention Deficit Hyperactivity Disorder (ADHD)
8,422 Patients Enrolled for Attention Deficit Hyperactivity Disorder (ADHD)
Shire Human Genetic Therapies, Inc.Industry Sponsor
5 Previous Clinical Trials
5,210 Total Patients Enrolled

Media Library

SMS Intervention (Behavioural Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT04189575 — N/A
Attention Deficit Hyperactivity Disorder (ADHD) Research Study Groups: SMS Intervention
Attention Deficit Hyperactivity Disorder (ADHD) Clinical Trial 2023: SMS Intervention Highlights & Side Effects. Trial Name: NCT04189575 — N/A
SMS Intervention (Behavioural Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT04189575 — N/A
Attention Deficit Hyperactivity Disorder (ADHD) Patient Testimony for trial: Trial Name: NCT04189575 — N/A
~16 spots leftby Jul 2025