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Clinical Trials/NCT04189536
NCT04189536
Unknown
Not Applicable

An SMS Intervention to Improve Adherence to Stimulant Medications in Adults With ADHD

Massachusetts General Hospital1 site in 1 country125 target enrollmentSeptember 19, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Attention Deficit/Hyperactivity Disorder
Sponsor
Massachusetts General Hospital
Enrollment
125
Locations
1
Primary Endpoint
Adherence to Stimulants
Last Updated
4 years ago

Overview

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).

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.

Registry
clinicaltrials.gov
Start Date
September 19, 2016
End Date
September 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Joseph Biederman, MD

Chief of the Clinical and Research Programs in Pediatric Psychopharmacology and Adult ADHD

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • Male and female adults 18 to 55 years
  • A diagnosis of Diagnostic and Statistical Manual Diploma in Social Medicine (DSM-V) Attention Deficit Hyperactivity Disorder based on clinical assessment
  • Is starting stimulant medication or has begun treatment with stimulant medication within six months of study enrollment
  • Proficient in English
  • Has a cellular phone with text messaging capabilities and is interested in and willing to receive text messages

Exclusion Criteria

  • Serious chronic medical or psychiatric condition that, in the investigator's opinion, puts the subject at risk for taking a stimulant
  • Pregnant or nursing females
  • Investigator and his/her immediate family
  • Unwilling/unable to comply with study procedures

Outcomes

Primary Outcomes

Adherence to Stimulants

Time Frame: 9 months

Adherence will be analyzed using the timeliness of stimulant medication prescription renewals over the 9 month period.

Study Sites (1)

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