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NCT04189575 Clinical Trial

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

Attention Deficit/Hyperactivity Disorder Clinical Trial

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

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT04189575
Other study ID # 2018-P-000591
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date May 24, 2018
Est. completion date December 2023

Study information
Verified date September 2022
Source Massachusetts General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 117
Est. completion date December 2023
Est. primary completion date June 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 55 Years
Eligibility 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

Study Design

Related Conditions & MeSH terms

  • Attention Deficit Disorder with Hyperactivity
  • Attention Deficit/Hyperactivity Disorder
  • Hyperkinesis

Intervention

Other:
• SMS Intervention
Delivery of text messages will use the Rip Road Mobile platform.

Locations
Country Name City State
United States Massachusetts General Hospital Boston Massachusetts

Sponsors (2)
Lead Sponsor Collaborator
Massachusetts General Hospital Shire Human Genetic Therapies, Inc.

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Adherence to Stimulants Adherence will be analyzed using the timeliness of stimulant medication prescription renewals over the 9 month period. 9 months
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