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

Phase 2

• Conditions: F06.7; Mild cognitive disorder

• Registration Number: DRKS00005652
• Lead Sponsor: Otto-von-Guericke Universität MagdeburgMedizinische Fakultät

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2014-01-22
• Study Completion: 2015-02-23
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

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

Exclusion Criteria

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

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
If the technical signal quality sufficient for<br>the quantitative assessment of the spontaneous EEG and event-related potentials?<br>Is the technical signal quality in the clinically relevant range comparable to a conventional EEG machine?

Secondary Outcome Measures

Name	Time	Method
The suitability of the new EEG machine in terms of handling for home monitoring?