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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 below
Select...
I am between 18 and 65 years old.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~throughout protocol
This trial's timeline: 3 weeks for screening, Varies for treatment, and throughout protocol for reporting.

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.

Find a Location

Who is running the clinical trial?

National Institute of Mental Health (NIMH)Lead Sponsor
2,913 Previous Clinical Trials
2,738,460 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

OPM MEG Clinical Trial Eligibility Overview. Trial Name: NCT04950309 — N/A
Normal Physiology Research Study Groups: OPM Array studies
Normal Physiology Clinical Trial 2023: OPM MEG Highlights & Side Effects. Trial Name: NCT04950309 — N/A
OPM MEG 2023 Treatment Timeline for Medical Study. Trial Name: NCT04950309 — N/A
~16 spots leftby Aug 2025