Recruiting

SCAP-Nerve

Sponsor:

Columbia University

Code:

NCT07539025

Conditions

Cervical Spinal Cord Plasticity

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Accepted

Interventions

SCAP

MagPro X100

Digitimer DS8R

Paired non-associative stimulation

Study Details

Brief summary:

Associative plasticity has been used to promote functional recovery from conditions affecting movement. Prior work from the Carmel laboratory has shown that paired associative stimulation protocols timed to converge in the cervical spinal cord induce significantly larger upper limb motor responses than if timed to converge in the motor cortex.

The goal of this prospective experimental study in typically developing adults is to test the effects of pairing sub-threshold hand motor cortical and median nerve stimulation targeted to induce plasticity in the cervical spinal cord, rather than in the motor cortex. Based on preliminary data, the investigators are performing a confirmatory study to test the physiological and behavioral effects of the paired brain and peripheral nerve protocol, called the SCAP-Nerve protocol.

This study will first be conducted in typically developing adults to confirm the cervical spinal cord as the ideal target and verify the present stimulation parameters are sufficient to promote induction of associative plasticity of sensorimotor connections for manual dexterity. The outcomes from this study could then be translated to efficacy studies in people with spinal cord injury and cerebral palsy to promote clinically meaningful improvements in dexterity.

Conditions

Cervical Spinal Cord Plasticity

Study ID

NCT07539025

Start date

May 9, 2026

Status verified date

May, 2026

Completion date

Jun, 2029

Anticipated

Primary completion date

Dec, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Accepted

Inclusion Criteria:

  • Willingness to participate in up to 4 sessions
  • Maintenance of caffeine and exercise levels at time of sessions
  • Ability to provide informed consent
  • No known central or peripheral neurological disease or injury
  • No known musculoskeletal injury of the tested arm or hand

Exclusion Criteria:

  • Personal or family history of seizures
  • Use of medications that lower seizure threshold
  • History of implanted equipment including stimulators/pacemakers

Study Design

Enrollment

20 participants

Anticipated

Allocation

Randomized

Intervention Model

Crossover

Primary purpose

Basic Science

Interventions and Outcome Measures

Arms

experimental: SCAP

With this session, participants will receive 90 trials of 0.1hz paired motor cortical stimulation and median nerve stimulation for 15 minutes at sub-threshold intensities, timed to converge in the cervical spinal cord simultaneously.

active comparator: Cortical stimulation only

With this session, participants will receive 90 trials of 0.1hz motor cortical stimulation for 15 minutes at sub-threshold intensities.

active comparator: Median nerve stimulation only

With this session, participants will receive 90 trials of 0.1hz median nerve stimulation for 15 minutes at sub-threshold intensities.

active comparator: Paired non-associative stimulation

With this session, participants will receive 90 trials of 0.1hz paired motor cortical stimulation and median nerve stimulation for 15 minutes at sub-threshold intensities, timed to be 40 milliseconds apart in the cervical spinal cord.

Interventions

SCAP

This utilizes pairing of repetitive transcranial magnetic stimulation (rTMS) and peripheral nerve stimulation (rPNS) timed to converge in the cervical spinal cord.

MagPro X100

This stimulator will be use to provide repetitive transcranial magnetic stimulation (rTMS).

Digitimer DS8R

This stimulator will be used to provide repetitive peripheral nerve stimulation (rPNS).

Paired non-associative stimulation

This utilizes pairing of repetitive transcranial magnetic stimulation (rTMS) and peripheral nerve stimulation (rPNS) timed to arrive at a pairing interval of 40 msec.

Primary outcome measure

  • Size of muscle response to brain stimulation after SCAP (percentage) [ Time Frame: 30 minutes after SCAP ]

Central Contacts and Locations

Central contacts

Shaker Dukkipati, MD, PhD

2123046501sd3850@cumc.columbia.edu

Jason Carmel, MD, PhD

jbc28@cumc.columbia.edu

Locations

Columbia University Irving Medical Center

Recruiting

New York, New York, United States, 10040

Contacts

More Information

Sponsor

Columbia University

Last update posted

May 22, 2026

Last verified

May, 2026

Keywords

  • cervical spinal cord
  • paired associative stimulation
  • motor evoked potential
  • spinal cord injury
  • cerebral palsy
  • manual dexterity
  • corticospinal
  • sensory afferent
  • SCAP
  • spinal cord associative plasticity

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Columbia University on 2026-05-22.