The Soterix Medical ElectraRx solution is a revolutionary software platform connecting stimulation administrators/clinicians and individuals with the data collected from Soterix Medical neuromodulation technologies and other third-party applications.
With full interoperability and the ability to share information across systems and platforms, ElectraRx can encourage individuals to engage in self-care, help administrators/clinicians to actively monitor sessions, reduce errors and adverse events, and encourage innovation. In a typical workflow, trial administrators/clinicians first enter individual information, then assign individual stimulation dose (when used in combination with Soterix Medical Neuromodulation device) and relevant self-assessments. Individuals access the ElectraRx platform with their unique login to respond to assessments, obtain stimulation session codes and enter device information back into the platform.
When used in combination with Soterix Medical approved trackers and other third-party applications, individual's vital signs and other relevant data can be entered into the ElectraRx platform. Trial administrators/clinicians can now visualize outcome progression and stimulation compliance on a real-time basis, gain valuable insight from aggregated data and may choose to adjust stimulation strategy on the fly. Trial administrators/clinicians also have a full overview of all individuals’ data.
ElectraRx Demonstration
Remote Neuromodulation Video
Typical flow involves stimulation administrators/clinicians first logging into ElectraRx portal using their unique login information. The administrators then select an enrolled individual and assign appropriate stimulation dose (intensity, duration, etc.). This activates the selected individual’s account. The administrators then assign the start and end dates of stimulation and pick the individual assessments to be collected.
At all times, the administrators have real-time access to the information collected by the individual’s device. They also have access to the individual’s historical data, symptoms, stimulation regimen compliance, and warning signs.
Typical flow involves individuals first logging into the ElectraRx portal using their unique login information. The portal will ask the individuals to answer self-assessments and clinical questionnaires, as assigned to them by the stimulation administrator/clinician.
The individual’s may be asked to perform custom tasks as guided by on-screen instructions. Individuals then proceed to perform a stimulation session. Finally, individuals enter relevant device information into the portal. The individuals account may also be used to collect sensor data such as vital signs, mobility, and data from other third-party applications.
Streamline and accelerate the recruitment process with e-consent.
Assign devices to patients/subjects and select treatment schedule.
Provide patients/subjects with pre and post stimulation assessments directly through the portal and track responses.
Patients/subjects automatically receive a new stimulation code for each scheduled session through the patient/subject portal.
Patients/subjects can enter device generated completion code at the end of each session, allowing practitioners to track compliance in real-time.
Practitioner contact information and ElectraRx tutorials are available to patients/subjects directly through the portal.
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