Safety, Feasibility, and Efficacy of TSCS on Stabilizing Blood Pressure for Acute Inpatients With SCI

Sponsor
Jill M. Wecht, Ed.D. (U.S. Fed)
Overall Status
Recruiting
CT.gov ID
NCT06000592
Collaborator
Icahn School of Medicine at Mount Sinai (Other)
50
1
1
57
0.9

Study Details

Study Description

Brief Summary

This site-specific project will focus on a novel non-pharmacologic approach to stabilizing BP during AIR after acute traumatic SCI. Current forms of pharmacologic and non-pharmacologic treatments for hypotension and OH remain inadequate in the SCI population. A critical need exists for the identification of safe, practical and effective treatment options that stabilize BP after traumatic SCI. Transcutaneous Spinal Cord Stimulation (TSCS) has several advantages: (1) does not exacerbate polypharmacy, (2) can be activated/deactivated rapidly, and (3) can be applied in synergy with physical exercise. TSCS represents an alternate approach to epidural SCS, with far greater potential to reach large numbers of individuals, thus providing for a greater likelihood of clinical implementation with far fewer risks. We are asking the key question: what if applying SCS earlier after injury could prevent the development of BP instability? To facilitate adoption of TSCS for widespread clinical use, we have designed a spatial-temporal mapping and parameter configuration approach that will result in a key deliverable for SCI care: a standard, easy to follow algorithm that will maximize individual benefits of spinal neuromodulation, while minimizing the burden on healthcare professionals. This project will provide the foundational evidence to support the feasible and safe application of TSCS for widespread clinical utility in the newly injured population, thereby overcoming barriers to engagement in prescribed AIR regimens that are imposed by ANS dysfunction.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Masking Description:
Participant awareness during TSCS appears to be unavoidable. The FDA recognizes that some trials of non-pharmacological interventions cannot be fully shammed or blinded, yet with careful blinding of data assessors, it is possible to obtain reliable results that meet FDA approval criteria.
Primary Purpose:
Treatment
Official Title:
Safety, Feasibility, and Efficacy of Transcutaneous Spinal Cord Stimulation on Stabilizing Blood Pressure for Acute Inpatients With Spinal Cord Injury
Actual Study Start Date :
Jan 1, 2022
Anticipated Primary Completion Date :
Aug 31, 2026
Anticipated Study Completion Date :
Oct 1, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: transcutaneous spinal stimulation

Device: Digitimer
transcutaneous spinal cord stimulation for blood pressure control following spinal cord injury.

Outcome Measures

Primary Outcome Measures

  1. The safety (#1) of TSCS to improve autonomic control following acute SCI. [Acute Inpatient Rehabilitation following SCI (up to 4 months)]

    Assess pain levels using a Likert Scale 0-10 (0=no pain, 10=worst pain).

  2. The safety (#2) of TSCS to improve autonomic control following acute SCI. [Acute Inpatient Rehabilitation following SCI (up to 4 months)]

    Document any skin changes (burns) following use of TSCS in count of occurrences.

  3. The efficacy (#1) of TSCS to improve autonomic control following acute SCI. [Acute Inpatient Rehabilitation following SCI (up to 4 months)]

    Blood pressure changes (mmHg) during the sit-up test with TSCS compared to no stimulation.

Secondary Outcome Measures

  1. The efficacy (#2) of TSCS to improve autonomic control following acute SCI. [Acute Inpatient Rehabilitation following SCI (up to 4 months)]

    To compare dizziness symptoms on a Likert Scale 0-10 (0=no dizziness, 10=worst dizziness) during the sit-up test with TSCS compared to no stimulation..

Eligibility Criteria

Criteria

Ages Eligible for Study:
14 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Newly injured patients with traumatic SCI

  • Admitted to Acute Inpatient Rehabilitation at Mount Sinai

  • Within one year of SCI

  • Seated hypotension (systolic BP ≤ 110 mmHg for males or ≤ 100 mmHg for females)

  • Orthostatic hypotension (fall in systolic BP ≥ 20 mmHg and/or a fall in diastolic BP ≥ 10 mmHg within 10 minutes of assuming an upright position)

  • Daily fluctuation in systolic BP ≥ 20 mmHg and/or fluctuation in diastolic BP ≥ 10 mmHg

  • At least 14 years old

Exclusion Criteria:
  • Implanted brain/spine/nerve stimulators

  • Cochlear implants

  • Cardiac pacemaker/defibrillator, or intracardiac lines

  • Open skin lesions on or near the electrode placement sites (neck, upper back)

  • Significant coronary artery or cardiac conduction disease

  • Recent history of myocardial infarction

  • Insufficient mental capacity to understand and independently provide consent

  • Pregnancy

  • Cancer

  • Deemed unsuitable by study physician

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Icahn School of Medicine at Mount Sinai New York New York United States 10029

Sponsors and Collaborators

  • Jill M. Wecht, Ed.D.
  • Icahn School of Medicine at Mount Sinai

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jill M. Wecht, Ed.D., Research Health Scientist, James J. Peters Veterans Affairs Medical Center
ClinicalTrials.gov Identifier:
NCT06000592
Other Study ID Numbers:
  • 1648740
First Posted:
Aug 21, 2023
Last Update Posted:
Aug 21, 2023
Last Verified:
Aug 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 21, 2023