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A Text Messaging (SMS) Intervention to Improve Adherence to Stimulant Medication in Adults With ADHD in the Primary Care Setting

A Text Messaging (SMS) Intervention to Improve Adherence to Stimulant Medication in Adults With ADHD in the Primary Care Setting

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04189575
Enrollment
117
Registered
2019-12-06
Start date
2018-05-24
Completion date
2023-12-31
Last updated
2022-09-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Attention Deficit/Hyperactivity Disorder

Keywords

Attention Deficit/Hyperactivity Disorder, ADHD, SMS Intervention

Brief summary

This study will assess the efficacy of the text messaging (SMS-based) disease management intervention to improve adherence to stimulants in adults with Attention Deficit/Hyperactivity Disorder (ADHD) within the Partners primary and psychiatry care settings. Participants in the study will receive customized text messages twice a day, every day, for a duration of 9 months. The text messages 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

Interventions

Delivery of text messages will use the Rip Road Mobile platform.

Sponsors

Shire Human Genetic Therapies, Inc.
CollaboratorINDUSTRY
Massachusetts General Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Masking description

All participants will be assigned to the text message intervention and therefore no masking is necessary.

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* Male and female adults ages 18-55 years * Receipt of a prescription for stimulant medication by their primary care physician or psychiatrist * Proficient in English * Has a cellular phone with text messaging capabilities and is interested in and willing to receive free of charge planned text messages

Exclusion criteria

* Investigator and his/her immediate family * Unwilling/unable to comply with study procedures

Design outcomes

Primary

MeasureTime frameDescription
Adherence to Stimulants9 monthsAdherence will be analyzed using the timeliness of stimulant medication prescription renewals over the 9 month period.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026