10 Participants NeededMy employer runs this trial

Optimizing Stimulation Techniques for Nervous System Monitoring

JR
Overseen ByJames R McIntosh, PhD
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

The purpose of this study is to better understand how electrical or magnetic stimulation affect the nervous system by optimizing the way researchers measure muscle responses. The relationship between stimulation intensity and muscle response is described by "neural recruitment curves," which are critical for monitoring the state of the nervous system during therapies like transcranial magnetic stimulation (TMS) and spinal cord stimulation (SCS).

This study tests a new, real-time computational approach based on our previously developed methods (Hierarchical Bayesian models) to estimate these recruitment curves more efficiently. The primary goal is to use this model to dynamically guide the experiment, automatically selecting the optimal stimulation intensities to test.

The investigators hypothesize that this optimized approach will accurately estimate the entire recruitment curve, or specific targets components of it like the motor threshold, using significantly fewer samples than standard methods. By reducing the number of measurements required, this approach aims to decrease experimental time and minimize participant burden, making future TMS and SCS therapies and experiments more feasible and efficient.

Who Is on the Research Team?

JR

James R McIntosh, PhD

Principal Investigator

Columbia University

Are You a Good Fit for This Trial?

Inclusion Criteria

I am a healthy adult.

Exclusion Criteria

History of seizures
History of autonomic dysfunction
I have had brain or nervous system surgery before.
See 3 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

1-2 weeks

Experimental Session

Participants undergo distinct experiments within a single session to compare different neurostimulation sampling algorithms.

1 hour
1 visit (in-person)

Follow-up

Participants are monitored for safety and effectiveness after the experimental session

2 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Adaptive Recruitment Curve Analysis

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Test of developed methodsExperimental Treatment6 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

Columbia University

Lead Sponsor

Trials
1,529
Recruited
2,832,000+

National Institute of Neurological Disorders and Stroke (NINDS)

Collaborator

Trials
1,403
Recruited
655,000+