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SMS Intervention for ADHD
Study Summary
This trial will test whether twice-daily text messages can improve adherence to stimulants in adults with ADHD.
- Attention Deficit Hyperactivity Disorder (ADHD)
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- Adults between 18 and 55 years old, regardless of gender.You are currently taking stimulant medication prescribed by your primary care doctor or psychiatrist.
- Group 1: SMS Intervention
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Are new participants being accepted into this experiment?
"At the moment, clinicaltrials.gov indicates that this research is not in search of participants; it was initially posted on May 24th 2018 and last updated September 22nd 2022. Nonetheless, there are 156 other trials currently recruiting patients."
Are there any qualifications that would enable me to partake in this trial?
"This clinical study is accepting 117 patients, aged 18-55, who have been diagnosed with Attention Deficit Disorder. In addition to meeting these requirements, participants must also own a mobile device capable of text messaging and be fluent in English. Furthermore, they are required to already possess a valid prescription for stimulant medication from their GP or psychiatrist."
Is participation in this experiment restricted to those over sixty or can younger individuals participate?
"This clinical trial requires that all potential participants are between 18 and 55 years of age."
Who else is applying?
What state do they live in?
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What portion of applicants met pre-screening criteria?
How many prior treatments have patients received?
Why did patients apply to this trial?
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