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EMMA App + Clinician Support for Cognitive Impairment (EMMA Trial)
EMMA Trial Summary
This trial studies an app-based system to help older adults with memory & daily activity management. It asks if clinician oversight is needed for use of the app.
EMMA Trial Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.EMMA Trial Design
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Who is running the clinical trial?
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- I have a diagnosed condition like stroke that explains my cognitive issues.I am 50 years old or older.I am unable to give my own informed consent.
- Group 1: Technology Support Only
- Group 2: Brief Clinician Motivational Support
- 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
Is there still capacity to recruit participants for this research?
"This clinical trial is still enrolling volunteers, as per the information on clinicaltrials.gov. It was initially posted on the 20th of January in 20203 and last modified a little over two weeks ago, on January 13th."
How many individuals are involved in participating in this investigation?
"Affirmative. According to clinicaltrials.gov, the trial in question is still trying to attract participants and was initially posted on January 20th of 2023 with a recent update made on January 13th of that same year. The investigators are looking for 50 individuals from one particular medical facility."
What primary objectives are researchers attempting to achieve through this experiment?
"The primary measure of success in this trial, which will be tracked over the 6-month duration to study completion, is Change in Daily Assessment of Independent Living and Executive Skills (DAILIES). Additionally, investigators are tracking Change in Everyday Compensation questionnaire (Ecomp), Change in Patient-Reported Outcome Measurement Information (PROMIS) System Applied Cognition scores, as well as a change in Self-Efficacy for Appropriate Medication Use Scale (SEAMS) score."
Who else is applying?
What site did they apply to?
What portion of applicants met pre-screening criteria?
Why did patients apply to this trial?
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