Becoming a User: Training and Authorization
- I. Becoming a User: Training and Authorization
- 1. MEG Orientation
- a. Users must schedule / attend an official MEG orientation to become familiar with the lab operations and equipment. Any personnel present in the MEG laboratory during acquisition must complete the MEG orientation, including all clinical support staff.
- 1. MEG Orientation
- 2. Authorized Independent User Requirements
- At least one of the persons in attendance at every MEG session must be authorized to operate the MEG independently. The authorization process involves several steps. To become authorized, the user is expected to become competent in performing all aspects of MEGs. MEG Core staff is available to provide training and technical assistance. Steps to becoming an authorized independent user appear below.
- 2. Authorized Independent User Requirements
- a. The first step in becoming an authorized independent user is to attend the MEG Orientation.
- b. Following completion of the orientation, each new user must assist with a minimum of two (2) MEG sessions, and independently perform one additional MEG session, in the presence of MEG Core facility staff or an authorized trainer. Additional observed sessions may be required to achieve competency. To request MEG Core Staff assistance/training use the MEG Core Staff Request Form (Under construction).
- c. Scientific staff in NIMH IRP labs at the doctoral level with at least one full year of experience as an independent user may be named as an authorized trainer at the discretion of the MEG core facility.
- d. Post-baccalaureate IRTA trainees can become authorized independent users, although they may not serve as authorized trainers.
- e. New users who have performed all procedures in the presence of MEG Core staff (or an authorized trainer) and have attained competency in all skills will be added to the authorized independent user list. The authorized independent user list and the authorized trainer list will be maintained by the lab manager and technologist, Judy Mitchell.
Required Personnel at MEG Sessions
When performing an MEG scan there must be at least two persons assisting with the study.
- Two people are required to be present during an MEG study, however, only one person must be capable of operating the equipment.
- When there is a subject in the MSR, at least one person must be available to observe the subject at all times. If the subject were to suddenly take ill, one person must remain with the subject and the other person should be available to go seek appropriate help.
- Two people are required to move / position the MEG chair, one person on each side, so that the chair glides evenly on the track and is not torqued to one side or the other which might damage or break the plexiglass track.
- Two people are required to place the MEG bed for supine recording.
MEG Orientation / Facility Tour
- Users must schedule / attend an informal MEG Orientation / Training to become familiar with the lab operations and equipment. During this training users will be instructed / assisted in filling out the MEG Facility Access Request which will establish a user account.
- Established users with new protocols will be required to complete a “new” Facility Access Request for each new protocol indicating the new protocol number.
Initiating a MEG Study
- Users must provide the director and/or staff scientist with a description of the research study design including information regarding setup requirements, software and equipment needs.
- Users must schedule a time to test their task / paradigm, equipment, software, etc. When scheduling indicate in the scheduling module description that the appointment is for:
- -- Equipment Testing - indicate that the appointment is for a “System Test or Equipment Test” (if technical support is needed indicate with staff support).
- -- Programming / Scripting - indicate "Programming / Scripting" and whether or not MEG staff assistance will be needed.
- -- Electrode Placement / "EOG/EEG/EMG" Montage Development - if assistance is desired indicate"technical assistance needed" with EOG/EEG/EMG electrode placement or setup. If you have a specific electrode setup or placement and require MEG Core staff assistance you must provide a detailed description of the objective and / or your setup.
- Most new studies, if not all, will also require "User Training" to test equipment, paradigms / programs and refine procedures with a test subject. Users must provide their own volunteer subject; if this is an external volunteer, he/she must be consented according to IRB guidelines. Usually this can be discussed and arranged during the MEG orientation tour.
- If you are piloting a new study, you must schedule time for User Training / Pilot Study via the web calendar as outlined below. Please indicate in the description that time is being requested for a “Pilot Study Setup, Pilot Study Observation or Pilot Study Practicum” so that MEG staff can be allocated as necessary.
For all scheduled MEG scans (including training and pilot studies) provide a simple, brief and accurate description of the protocol or paradigm indicating if any special equipment, assistance or setup is needed.
MEG Training / Pilots
There is a three–step training program specifically designed so that users know how to to operate MEG equipment, can conduct a scan from start to finish and acquire practical experience under the guidance of MEG staff. The pilot is designed so that the user can become competent in performing all aspects of MEGs on their own subjects. MEG Core staff is available to provide pilot training and technical assistance as needed or requested. This training must be arranged with MEG staff and then scheduled via the MEG calendar.
- ♦Pilot / Instruction/Setup – (without a subject) MEG training, setup instructions and equipment operation with the assistance of MEG staff.
- ♦Pilot / Observation – (with a subject) instructions and observation of MEG setup and scan with the assistance of MEG staff.
- ♦Pilot / Practicum – (with a subject) hands on training session running a subject during a MEG scan under the observation of MEG staff.
- Users must provide their own volunteer subject for training; if this is an external volunteer, he/she must be consented according to IRB guidelines.
- User training must be scheduled via the web-based calendar indicating that the appointment is for specific training, i.e., "Training - Instruction", "Training - Observation", "Training - Practicum" so that we can schedule the proper MEG personnel to assist with the training.
Subject Registration & Consenting
All subjects participating in MEG studies are required to have a valid medical record number (Medical Information System /MIS #).
- It will be the responsibility of the principal investigator (PI) to make sure that all outpatients and control subjects have gone through the appropriate registration process and have a valid MIS#.
- A doctor’s order is not required for an MEG scan but a progress note must be placed in the subject’s chart indicating the nature of the scan performed, the date, time, and protocol number. The patient’s condition and general performance should also be noted. The progress must also be signed by the appropriate personnel.
- An IRB approved consent form must be signed by all subjects prior to participating in any MEG research study.
- Investigators are required to satisfy all Clinical Center documentation requirements.
- It will be the responsibility of the PI to assure that subjects have signed the appropriate consent form.
Although MEG/EEG poses no known risk to subjects, certain physical conditions may make subjects ineligible to participate in scanning. Some subjects will be ruled out for participation in scanning due to factors involving metallic foreign bodies which may prevent obtaining artifact free data. It will be the responsibility of the PI to pre-screen subjects for the below listed contraindications during the selection process.
Conditions That Will Rule Out a Subject:
- Cardiac Implants - Cardiac pacemaker / Cardiac or neural defibrillators
- Magnetic Implants - Any magnetic implantation / Implants made from iron (ferrous products)
- Mechanical Implants - Any mechanical implantation; any thing that has a motor
- Head Size - any head size greater than 59-60 cm; subject’s head is too large to fit in the helmet
- Weight - when using the chair the weight limit is about 300 lbs; for the bed it is about 250 lbs
All MEG subjects should be screened for the following items which may cause recording artifact.
- -Surgical aneurysm clips
- -Intra-orbital metallic structures
- -Implanted pumps (i.e., Insulin pumps)
- -Metal plates, pins or bolts in head
- -Steel pins from root canals; a permanent retainer
- -Ear implants (certain cochlear implants)
- -Metal rods, plates or screws in the body or mouth
- -Previous surgery (if metal was left in the body)
- -Hearing aids (should be removed before scanning)
- -Braces (causes severe artifact)
- -Tattoos (may have metallic ink)
Users/PIs are responsible for giving subjects instructions prior to any scheduled procedure.
- Subjects should be informed not to wear these items:
- Bras with underwires
- Makeup - mascara, eye liner, eye shadow or anything with glitter
- Clothing containing metallic (shiny) threads or glitter
- Metal on clothing -i.e., metal buttons, snaps or trimming
- Subjects should be informed that metallic/magnetic items should not be taken into the Magnetically Shielded Room (MSR). These include such items as:
- -Cell phones
- -Credit Cards
- -Small metal objects such as hair pins, paper clips, safety pins, etc.
- -Shoes (may have metallic dust particles on them)
- -It is the responsibility of the PI to inform subjects that if they arrive unprepared i.e., have metallic/magnetic parts on their clothing that cannot be easily removed, they may be asked to change into non-magnetic clothing which will be provided by staff.
- -If there is any question about whether an object is magnetic, the object is not taken inside the MSR.
- -In order to help inpatients become familiar with MEG an inpatient orientation tour may be scheduled at the discretion of the PI or nursing staff.