Your session is about to expire
← Back to Search
OPM MEG Brain Activity Mapping
N/A
Recruiting
Led By Allison Nugent, Ph.D.
Research Sponsored by National Institute of Mental Health (NIMH)
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Male or female, aged 18-65
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up throughout protocol
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing a new sensor called OPM that measures brain activity by detecting magnetic fields. These sensors can be placed directly on the scalp and offer advantages over traditional methods. It targets healthy adults aged 18-65 who have had an MRI scan. The sensors are placed on a cap and can accurately measure the brain's magnetic fields.
Who is the study for?
Healthy adults aged 18-65 who've had an MRI scan under a specific protocol can join this study. They should be in good health, able to follow the study's procedures, and available for its duration. People with metal in their body that affects MEG recordings cannot participate.
What is being tested?
The trial is testing a new brain activity sensor called OPM against the traditional SQUID MEG. Participants will wear special equipment on their head and complete tasks involving touch, sight, sound, or language stimuli while magnetic fields are measured.
What are the potential side effects?
There are no significant side effects expected from participating in this trial as it involves non-invasive measurement of brain activity using advanced imaging technology.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am between 18 and 65 years old.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ throughout protocol
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~throughout protocol
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
array characterization metrics
Secondary study objectives
Somatotopic representations
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: OPM Array studiesExperimental Treatment2 Interventions
Testing of a final 49-61 channel OPM MEG system and any interim arrays
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Treatments like transcranial magnetic stimulation (TMS) and other neuromodulation techniques work by using electromagnetic fields to modulate neural activity in the brain. These treatments can alter brain function, potentially improving symptoms in various neurological conditions by targeting specific areas of the brain.
This is particularly relevant for patients as it helps them understand how these treatments can influence brain activity and contribute to their overall neurological health.
Effect of transcranial pulsed electromagnetic fields (T-PEMF) on functional rate of force development and movement speed in persons with Parkinson's disease: A randomized clinical trial.
Effect of transcranial pulsed electromagnetic fields (T-PEMF) on functional rate of force development and movement speed in persons with Parkinson's disease: A randomized clinical trial.
Find a Location
Who is running the clinical trial?
National Institute of Mental Health (NIMH)Lead Sponsor
2,918 Previous Clinical Trials
2,739,841 Total Patients Enrolled
5 Trials studying Normal Physiology
3,852 Patients Enrolled for Normal Physiology
Allison Nugent, Ph.D.Principal InvestigatorNational Institute of Mental Health (NIMH)
1 Previous Clinical Trials
340 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am between 18 and 65 years old.
Research Study Groups:
This trial has the following groups:- Group 1: OPM Array studies
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Share this study with friends
Copy Link
Messenger