Embrace: Seizure Characterization

Empatica

Status: Invitation-only

Conditions: Epilepsy

Treatments: Device: Embrace + Alert App

Study type: Interventional

Funder types: Industry

Identifiers

NCT03206502

2016-001

Details and patient eligibility

About

The study is intended to characterize sleep, stress, and seizures in daily life with the Empatica Embrace watch and smartphone-based diary-alert system. The primary study objective is to collect and validate biometric signals from epilepsy patients using the Empatica Embrace watch and compare them to ictal events captured from human (patient and caregiver) reports.

Full description

Patients use the Embrace sensor with a smartphone app, "Alert". The sensor attempts to capture convulsive seizure events such as generalized tonic-clonic seizures (GTCS's), and to initiate an alert when such an event is captured. Patients can also enter seizures (captured or not, GTCS or not) into the "Mate" diary, and they can cancel or mark false alarms if Embrace triggered a false alarm.

Enrollment: 100,000 estimated patients

Sex: All

Ages: 1 to 99 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Participants must be between the ages of 1-99
• Anyone (healthy or not) can participate
• Adult participant must either be able to give consent or must have an acceptable surrogate capable of giving consent on their behalf.
• Participants under age 18 must have an adult guardian give informed consent, and if capable, the patient must give informed assent.
• Participants with GTCS must have a functioning smartphone (iOS or Android) that can be paired with the Embrace over a Bluetooth Low Energy connection and agree that it can be kept on or near their person.
• Participants with GTCS (or their surrogate) must be able to identify one or more "designated frequent caregivers," who has a functioning phone, agrees to keep it regularly charged, agrees to receive alerts, and agrees to respond to alerts promptly to the best of their ability.
• Participants must be fluent in the language of the consent forms (Currently limited to English but Spanish and other languages are planned).
• Participants must reside in the United States.

Exclusion criteria

• Participants must not have broken or injured skin at the wrist or leg location where Embrace is worn, and they must be able to tolerate wearing Embrace snugly for long periods of time. Thus, they should not have allergies to the material composition of the Embrace watch, or discomfort wearing a wristwatch or leg-band device.
• Participants should not be homeless.
• Participants should not have active dependence on substances that are not currently prescribed by their doctor (e.g. alcohol, pain medications, illegal drugs) or be taking substances that they are not willing to disclose as a study participant.
• Participants must not be pregnant or planning to become pregnant within six months at the time of screening.

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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100,000 participants in 1 patient group

Embrace+Alert App

Experimental group

Description:

Participants are allowed to enter the trial (to use Embrace+Alert app) whether or not they have epilepsy. People without epilepsy may use Alert in this trial even though they are not expected to have seizures, as long as they are willing to mark false positives. Since many people with epilepsy live active lives and appear perfectly healthy outwardly, it is important that their active lifestyle data not trigger false alarms. Allowing healthy participants without epilepsy to contribute active lifestyle data helps us make the detection algorithm even stronger and better.

Treatment:

Device: Embrace + Alert App