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Wearable Devices to Monitor Seizures in Autoimmune Epilepsy

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Mayo Clinic

Status

Completed

Conditions

Healthy
Autoimmune Epilepsy

Treatments

Device: Biosensor

Study type

Interventional

Funder types

Other

Identifiers

NCT05627661
22-006702

Details and patient eligibility

About

The purpose of this research is to search for reproducible changes in a wide range of physical signals, including heart rate, muscle tone and activity and EEG before and at the onset of seizures in patients with epilepsy.

Enrollment

33 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients diagnosed with or suspected of having autoimmune epilepsy.
  • Normal controls - cognitively normal subjects without epilepsy

Exclusion criteria

• Cognitive or psychiatric condition rendering patient unable to cooperate with data collection or manage and recharge smart watch and tablet computer devices. Presence of open or healing wounds near monitoring sites (infection risk).

Trial design

Primary purpose

Basic Science

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

33 participants in 2 patient groups

Autoimmune Epilepsy with Biosensors
Experimental group
Description:
Subjects with suspected autoimmune epilepsy will wear biosensors on wrist or upper arm during the at home monitoring period.
Treatment:
Device: Biosensor
Healthy Controls with Biosensors
Active Comparator group
Description:
Neurologically normal adult healthy controls will wear biosensors on wrist or upper arm during the at home monitoring period.
Treatment:
Device: Biosensor

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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