Founder of a platform that optimizes patient-trial matches.
Apr 6, 2020 11:24:06 GMT -5
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Post by Deleted on Apr 6, 2020 11:24:06 GMT -5
Dear all,
Over the next year, many mobile applications will be developed that allow patients to access medical data from their phone, increasing the transferability of medical information in the United States (https://www.healthit.gov/cureule/what-it-means-for-me/patients).
As a result of this policy, I am in the process of creating a platform that allows patients to share their de-identified medical data with clinical trial recruiters to optimize patient-trial matches.
Simplified, the patient will essentially consent to distributing their medical data to clinical-trial affiliates that are on the platform and the recruiter will have the ability to cross-reference patient data to determine if the patient is a match for their study based on patient-trial selection criteria. The patient will be automatically notified if they are a match for their study before having to communicate directly with a recruiter. Patients will be able to specific criteria such as pmity, compensation, and duration of the trials they are looking for.
The idea is to streamline the process of joining a clinical trial, decreasing the time and expense required by the patient and the recruiter to identify viable matches, increase proportion of patients that enroll in clinical trials for financial and/or health reasons, and to allow patients to enroll in more trials than they otherwise would have (increasing income, treatment availability, etc).
I am interested in talking to the good people of this forum who consider themselves part or full-time "guinea pigs" to get an in-depth understanding of what difficulties they face when enrolling in a clinical trial, and if a platform, such as the one I am proposing, would have utility in their capacity as subscribers of clinical trials.
If you are interested in communicating further, please message me privately.
All the best,
jeryco06
Over the next year, many mobile applications will be developed that allow patients to access medical data from their phone, increasing the transferability of medical information in the United States (https://www.healthit.gov/cureule/what-it-means-for-me/patients).
As a result of this policy, I am in the process of creating a platform that allows patients to share their de-identified medical data with clinical trial recruiters to optimize patient-trial matches.
Simplified, the patient will essentially consent to distributing their medical data to clinical-trial affiliates that are on the platform and the recruiter will have the ability to cross-reference patient data to determine if the patient is a match for their study based on patient-trial selection criteria. The patient will be automatically notified if they are a match for their study before having to communicate directly with a recruiter. Patients will be able to specific criteria such as pmity, compensation, and duration of the trials they are looking for.
The idea is to streamline the process of joining a clinical trial, decreasing the time and expense required by the patient and the recruiter to identify viable matches, increase proportion of patients that enroll in clinical trials for financial and/or health reasons, and to allow patients to enroll in more trials than they otherwise would have (increasing income, treatment availability, etc).
I am interested in talking to the good people of this forum who consider themselves part or full-time "guinea pigs" to get an in-depth understanding of what difficulties they face when enrolling in a clinical trial, and if a platform, such as the one I am proposing, would have utility in their capacity as subscribers of clinical trials.
If you are interested in communicating further, please message me privately.
All the best,
jeryco06