EEG Lab Arts Standard Operating Procedure Version 2.3
EEG Lab Arts Standard Operating Procedure Version 2.3
Standard
Operating
Procedure
Version 2.3 March 2016
Figures ……………………………………………………………………......…….… 13
The most important thing to remember when recording EEG is that there is no substitute
for clean data. While filters and other transformations can be applied to data after
recording, these can have adverse effects on the quality of the signal. Therefore, every
artefact-free as possible.
In the lab
In general, if you use the EEG laboratory, you should leave it as you would like to find it.
With an increasing amount of users and experiments being run, time in the lab can be at a
premium. Thus, time spent before a session having to clean up or rearrange after the last
user is time wasted, especially when a participant is waiting. EEG sessions are time
consuming for participants so having them waiting while the lab is being prepared is to be
avoided. Having your participant in the chair for any time longer than is necessary can
increase the likelihood of fatigue, with concurrent lapses in concentration and potential
decreases in motivation and performance. Besides reducing the risk of these adverse
confounds, an efficient manner in the laboratory with the participant serves to promote
Most experiments can be run using the same hardware set-up (i.e., computers, monitors,
amplifier, electrodes, etc.). In the recording booth, there is a monitor for users to see the
recording computer output, allowing the impedance meter to be seen, as well as allowing
the participants to see their own EEG signal. Do not switch cables from
cables can be difficult to fathom, especially when a participant is waiting. If you must do
this, remember to reconnect them to their original positions after your session.
The computers in the lab are to be used for experiment-related activities only. Only use
Brainvision EEG software requires USB ‘dongles’ for use, a separate dongle for
recording and analyzing data. You should find these in the USB ports of the recording
computer. The E-Prime program on the stimulus PC also needs a dongle. Under no
circumstances are any of these dongles to be removed from the computers. Never
download any software to any computer in the lab without the express permission of a
member of staff. If you require updates or solutions from the Brain Products website,
contact a technician.
Before your session, make sure that the amplifier is working by taking the following steps
2. On the EEG recording computer, open Brain Vision Recorder. Within this
3. Click ‘Monitor’.
4. A blank signal should appear. This ensures that the recording software is
6. Turn on the computer which will present the tasks. Have your task(s) ready.
use. This is very important as water or excess gel can cause the smearing or
‘bridging’ of the signal across electrode sites, leading to artefacts in the data.
8. Prepare the other consumables for the recording if they are not already laid out.
This includes ensuring adequate supplies of tissues, cotton-tipped buds, EOG ring
stickers and holders, alcohol solution and syringes filled with electrode gel. Lay
these out on the table for easy access during the session.
When the participant arrives, seat them on the chair in front of the monitor. Put
the ‘Testing in Progress’ sign on the door. Measure the circumference of their head using
the measuring tape which is hung on the handle of the door. This dictates which cap is to
be used (i.e., if the head circumference is 54cm, use the cap labelled ‘54’).
Attach the electrodes to this cap (Note: you may have met the participant at a pre-testing
session. If so, that is a good time to measure the head circumference, allowing you to
prepare the right cap in advance of the session). Ask the participant which form of
strapping they would prefer; the chin strap or chest strap. Remember to measure the
projection of the occipital bone at the rear part of the skull) before putting the cap on (see
Figure 1). This allows you to position the cap correctly. To decide where the cap sits,
calculate 10% of the nasion-inion distance, and measure this distance from the nasion up
along the forehead. This is the place where the front of the cap should lie.
If this is done correctly, all the electrodes on the cap should be located at the correct sites.
When they have decided which strap they prefer, put the cap on and fasten it with this
strap. When the cap is in place, the participant is ready to be gelled up.
1. With the cap in place, use a cotton swab to part the hair in the centre of each
2. Clean the scalp/skin in the centre of each electrode using a cotton swab and the
alcohol solution.
3. Fill the centre of each electrode with gel using a syringe, making sure to start
injecting the gel at the skin and withdrawing the syringe as you push the gel out.
5. The impedance indicator is located on the far right of the screen; change to 0-20
kΩ. Aim to get the impedance as low as possible; below 10KΩ is desirable.
7. Attach VEOG and HEOG electrodes to measure eye movements. Place the VEOG
electrodes above and below the centre of the eye (ensuring bottom electrode is
below delicate skin under the eye). Place HEOG electrodes on each temple, with
the centre of the electrodes in line with the centre of the eyes (see Figure 2).
When the impedance at each electrode is low enough and EOG electrodes are in place,
recording can begin. Since movement artefact negatively impacts on signal quality in a
their own EEG signal. This can be done by exiting from the impedance mode in Recorder
The EEG signal should now be visible both on the main recording monitor in the lab and
the monitor in the recording cubicle. To illustrate the extent of interference caused by eye
blinks and movement, ask the participant to watch their signal as they blink, cough, grind
their teeth etc. This method normally proves very useful in minimising movement artefact
in the data.
Blinking:
Grinding Teeth:
When you are ready to begin recording click Play/resume recording on the toolbar
Enter your file details and click ‘Save’. Note: make sure that you are recording to the
When the session finishes, you must stop recording the EEG signal by pressing the ‘Stop’
Then, in order to terminate monitoring status, click the ‘Stop Monitoring’ button on the
toolbar
Take the cap off the participant, paying particular attention when unclipping from the
chest strap, as the clips may snap up and hit the participant’s chin which can be painful.
Peel the cap off from the front backwards. Be wary of sites where hair has been tangled
with the electrode; tugging at these sites can be painful, especially when hair is long.
the ‘Testing in Progress’ sign down from the door. Bring the participant to the bathroom,
and remember to bring the key with you. This should be in the plastic pocket in the top
drawer of the locker. Show them the sink and shampoos and show them how to lock the
door. Ask them to return to the EEG lab when they are finished to sign any debriefing (or
other) forms. While they wash their hair, there is a good opportunity to save/transfer
their behavioural data and prepare the lab for cleaning. It also allows forms and any other
General housekeeping
1. Do not remove the EEG electrodes from the amplifier. For cleaning and other
be brought to the lab. Always cover the amplifier with a towel before bringing
2. When removing the electrodes from the cap, slide them forward gently towards
the open end of the electrode adaptor. If this proves difficult, use a pen to push it
is delicate.
3. Do not snap the electrodes upwards. Slide them out of the adaptor.
4. Wash the electrodes individually in the basin of water. While you are doing this,
5. Use a toothbrush to scrub gel from electrode surfaces. Electrodes can be gently
patted dry with a towel. It is important to ensure that all gel is removed from the
electrodes after each use. Clean electrodes are essential for proper
measurement.
6. As you wash the electrodes, pay attention to the surface of each, noting any cracks
or build-up of residue on the surface. Never ignore these problems – they are of
7. When the electrodes are washed, place them on a towel on the table with the amp.
Only attach them to a cap if you know the head circumference of the next
9. Wash EEG cap using lukewarm water. This can be done in the bathroom sink.
Use a toothbrush to remove any gel from electrode adaptors in the cap. Rinse in
10. Place the cap on a polystyrene head while it is still wet and hold in place using a
chin-strap. This ensures that the caps do not lose their shape.
11. Empty the syringes of excess gel and clean, both inside and out. Dry gel in the
syringes causes the rubber seal to come away from the plunger.
12. Wipe down the table, cleaning away any dried gel, using some tissues dipped in
lukewarm water.
13. Arrange electrodes, cap, gel, syringes, cotton swabs, isopropylalcohol solution,
EOG washer-stickers and tissues for the next data collection session, regardless of
The men’s and ladies’ bathrooms on the top floor have shower and hair washing facilities
intended for use with the EEG Lab. These bathrooms are used for two main purposes: for
cleaning the caps, and for participants to wash their hair. It is important that these
bathrooms are kept very clean. In your pre-testing routine, prepare the bathroom with the
following:
1. The grey basin for cleaning the electrodes after the session;
2. The sink and drip tray has been cleaned. After cleaning caps in the sink and while
the sink is still wet, it may appear clean. However, as the surface dries, residual
gel will appear like a sandy deposit. Ensure that this is cleaned away before your
session begins. The surface must be wiped with a cloth/tissue/used towel; running
3. An ample supply of towels. Check the press to make sure that there are enough
towels for all your participants of the day. Also, check the online calendar (see
below) to see if participants are scheduled for the next day. If they are, make sure
there are at least some towels for them too. If not, or in any circumstance where
you finish the supply of clean towels, you must take them home and wash a load.
Never leave the bathrooms with no clean towels, even if you have no more
participants coming. If the supply is nearing its end and another user has
5. Bring a basin of warm water with you to the lab before the session begins. This
will be used at the end to clean the electrodes and saves you having to fill it while
When you are planning your sessions in the lab, check the lab’s online calendar. This can
be found on www.gmail.com. The user name for this account is ‘nuigeeg’. Another user
or your supervisor will give you the password, which changes periodically. Here you can
book time in the lab, either for experiments or analysis. A few points to note:
1. Avoid booking the lab to keep slots in case you get a participant or in case you
2. When you book it, detail what you plan to do (e.g., running experiments,
analysis).
3. If you are flexible about using it, note this in the description. This allows others,
who may have difficulty recruiting participants, to ask for your slot should a
Figure 1.
Vertical electro-oculogram
Horizontal electro-oculogram
Researchers should familiarise themselves with applicable sections of the PSI’s Code of
during the research session. Attention should be paid to ensure that the participant is not
Air quality in the booth may deteriorate during a lengthy session – it may be necessary to
open the test booth door and run a fan to circulate air, if the air-conditioning is turned off.
the research at any time, and arrange a means for the participant to signal that they would
like to take a break. It would also help in this context, if the runs of trials were not
excessively long, and the participant had the option to delay the start of the next run, so
they could take a break. Be sensitive to any signs of distress shown by a participant in the
If a participant reports irritation from the electrode gel, or discomfort from the EEG cap
device attached to the participant. There may also be other trailing cables in the setup,
depending on the research protocol, attached to such items as PCs, monitors, speaker
systems, etc.
While it is not possible to eliminate all such cabling, researchers are obliged to minimise
any resulting trip hazard. Re-routing cables, and using extension cables for mains, VGA,
USB, and PS/2 (legacy mouse/keyboard) leads, may reduce the risk to an acceptable
level. The use of floor mats may also serve to reduce the trip hazard.
Researchers should be mindful that however familiar they are with the research setup, it
will be new to participants, so it is imperative that any unresolved trailing cables are
brought to their notice – this applies to every participant, every time! Under no
tension) be left in the natural path from the entrance door to the participant’s seat.
Researchers should consider whether there would be any benefit from turning the
research setup through 90o or 180o, with a view to re-siting cables out of harm’s way.
In the case of fire, researchers must disengage the participant from any recording
equipment to which they are attached. It would be best if this resulted in the participant
being free of all cables, but if it proves painful or impractical to remove e.g. the EEG cap,
quickly, then it may be better to disconnect the amplifier and evacuate with the
Move quickly to the nearest stairwell, and lead the participant out of the building. Stay at
the assembly point outside the main front door until further instructions.
The access door to the Sound Lab is not to be jammed open at any time. If swipe access is
required to the lab for legitimate research purposes, then that can be arranged through
The software dongles for Brainvision Recorder, Brainvision Analyser, and E-Prime are
Research setups belonging to another researcher’s study are not to be interfered with,
except with the consent of the other researcher. If the existing setup is preventing work on
a new researcher’s study, then it should be brought to the attention of the existing
by
Dr. Michael A. Keane