Evaluation of an EEG system with dry electrodes and wireless links (MYND) compared to a conventional EEG recorder

Evaluation of an EEG system with dry electrodes and wireless links (MYND) compared to a conventional EEG recorder - MYND

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

DRKS

Registry ID

DRKS00005652

Enrollment

Registered

2014-01-22

Start date

2014-02-03

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

F06.7

Interventions

Group 1: 20 patients with mild cognitive impairment: For each subject, measurement will be done at first with the new device (with dry electrodes and wireless links (MYND e1020x)) and then with the co

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: • Age> 18 years • capacity to consent - patients with MCI - healthy persons

Exclusion criteria

Exclusion criteria: Patients with MCI: • tremor Infectious disease Known epilepsy Patients who are not in a position to cope Study Procedure without the caregiver

Design outcomes

Primary

Measure	Time frame
If the technical signal quality sufficient for the quantitative assessment of the spontaneous EEG and event-related potentials? Is the technical signal quality in the clinically relevant range comparable to a conventional EEG machine?	—

Secondary

Measure	Time frame
The suitability of the new EEG machine in terms of handling for home monitoring?	—

Countries

Germany

Contacts

Public ContactAnne Katrin Baum

Universitätsklinikum AöRKlinik für Neurologie

anne.baum@med.ovgu.de+49-391-67-15022

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026