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Investigation of the effects of cognitive states on sensory gating and motor output

Organizational Data

DRKS-ID:
DRKS00016909
Recruitment Status:
Recruiting ongoing
Date of registration in DRKS:
2019-12-17
Last update in DRKS:
2019-12-17
Registration type:
Retrospective

Acronym/abbreviation of the study

No Entry

URL of the study

No Entry

Brief summary in lay language

The aim of this project is to investigate the influence of sensory perception (i.e. Vision, Hearing and Touch) on motor processes, that means different movement patterns. Specifically we are interested how different cognitive states, for example Fatigue or Motivation affects the coupling between sensory perception and motor processes. We hope that by understanding the brain processes in healthy participants provide us with new methods for the future treatment of patients, for example after stroke.

Brief summary in scientific language

Reinstating the mechanisms of sensory processing and motor control is an important goal to advance treatment of neurological and neuropsychiatric diseases which are often associated with a loss of sensorimotor function. However, before one can design such therapies, in depth knowledge regarding the mechanisms governing sensory processing and motor control in healthy human subjects is required. In particular, little is known about how the current cognitive state (e.g. amount of fatigue or motivation) affects the integration of sensory information into a motor command. To fill this gap of knowledge, we will therefore investigate how integration of sensory information (i.e. vision, audition, somatosensation) shapes motor output and more importantly how this integration is affected by the current cognitive state (i.e. motivation or fatigue). We will use a multimodal approach to the solve this problem, i.e. we will combine neuroimaging methods (MRI, EEG) as well as non-invasive brain stimulation methods (NIBS; i.e. TMS, tCS) and peripheral nerve stimulation (PNS) with behavioural tests.

Health condition or problem studied

Free text:
Basic research in healthy participants
Free text:
Healthy participants
Healthy volunteers:
Yes

Interventions, Observational Groups

Arm 1:
The project involves neurophysiological measurements (e.g. fMRI, EEG and EMG) as well as non-invasive brain stimulation (e.g. TMS, tCS) during behavioural tests (e.g. sensorimotor and cognitive tasks).

Endpoints

Primary outcome:
Electrophysiological markers of brain activity as measured with EEG (Electroencephalography). BOLD (blood oxygenation level dependent) signal changes as measured with fMRI (Functional magnetic resonance imaging). Muscle activity as measured with EMG (Electromyography). Performance on behavioural tasks (accuracy, reaction time, and others). Eye and motion tracking measures. The planned end date of the study is 1. September 2024.
Secondary outcome:
Not applicable

Study Design

Purpose:
Basic research/physiological study
Retrospective/prospective:
No Entry
Study type:
Non-interventional
Longitudinal/cross-sectional:
No Entry
Study type non-interventional:
No Entry

Recruitment

Recruitment Status:
Recruiting ongoing
Reason if recruiting stopped or withdrawn:
No Entry

Recruitment Locations

Recruitment countries:
  • Switzerland
Number of study centers:
Monocenter study
Recruitment location(s):
  • Other Eidgenössische Technische Hochschule Zürich Zürich

Recruitment period and number of participants

Planned study start date:
2018-09-01
Actual study start date:
2018-09-01
Planned study completion date:
No Entry
Actual Study Completion Date:
No Entry
Target Sample Size:
750
Final Sample Size:
No Entry

Inclusion Criteria

Sex:
All
Minimum Age:
18 Years
Maximum Age:
65 Years
Additional Inclusion Criteria:
Healthy participants Age 18 – 65 years Normal physical and mental health Normal or corrected to normal vision

Exclusion Criteria

Known history of neurological, musculoskeletal or neuromuscular disorders. Pregnancy. Participants with metal implants in their body including pacemakers, or electronically/magnetically/mechanically activated implants.

Addresses

Primary Sponsor

Address:
NCM-Lab, ETH Zürich
Prof. Dr. Nicole Wenderoth
Auguste-Piccard-Hof 1
8093 Zürich
Switzerland
Telephone:
+41 44 635 61 55
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
No Entry
Investigator Sponsored/Initiated Trial (IST/IIT):
Yes

Contact for Scientific Queries

Address:
NCM-Lab, ETH Zürich
Prof. Dr. Nicole Wenderoth
August-Piccard-Hof 1
8093 Zürich
Switzerland
Telephone:
+41 44 635 61 55
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
No Entry

Contact for Public Queries

Address:
NCM-Lab, ETH Zürich
Prof. Dr. Nicole Wenderoth
Auguste-Piccard-Hof 1
8093 Zürich
Switzerland
Telephone:
+41 44 635 61 55
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
No Entry

Principal Investigator

Address:
NCM-Lab, ETH Zürich
Prof. Dr. Nicole Wenderoth
August-Piccard-Hof 1
8093 Zürich
Switzerland
Telephone:
+41 44 635 61 55
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
No Entry

Sources of Monetary or Material Support

Institutional budget, no external funding (budget of sponsor/PI)

Address:
NCM-Lab, ETH Zürich
Auguste-Piccard-Hof 1
8093 Zürich
Switzerland
Telephone:
+41 44 635 61 55
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
No Entry

Ethics Committee

Address Ethics Committee

Address:
Kantonale Ethikkommission Zürich [Kantonale Ethikkommission Zürich ]
Stampfenbachstrasse 121
CH-8090 Zürich
Switzerland
Telephone:
No Entry
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
http://www.kek.zh.ch/internet/gesundheitsdirektion/kek/de/home.html

Vote of leading Ethics Committee

Vote of leading Ethics Committee
Date of ethics committee application:
2018-06-20
Ethics committee number:
BASEC-Nr. 2018-01078
Vote of the Ethics Committee:
Approved
Date of the vote:
2018-08-23

Further identification numbers

Other primary registry ID:
No Entry
EudraCT Number:
No Entry
UTN (Universal Trial Number):
No Entry
EUDAMED Number:
No Entry

IPD - Individual Participant Data

Do you plan to make participant-related data (IPD) available to other researchers in an anonymized form?:
Yes
IPD Sharing Plan:
Anonymised measurement data can only be made available to other research groups if participants sign the corresponding separate written consent form for further data use. The written consent allows both the sharing of anonymized data upon request as well as upload of the data to scientific databases. This agreement does not expire.

Study protocol and other study documents

Study protocols:
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Study abstract:
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Other study documents:
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Background literature:
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Related DRKS studies:
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Publication of study results

Planned publication:
No Entry
Publikationen/Studienergebnisse:
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Date of first publication of study results:
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DRKS entry published for the first time with results:
No Entry

Basic reporting

Basic Reporting / Results tables:
No Entry
Brief summary of results:
No Entry