Remotely Delivered Cognitive Multisensory Rehabilitation for Sensory and Motor Recovery After Spinal Cord Injury

Sponsor
University of Minnesota (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05870189
Collaborator
(none)
22
1
2
24
0.9

Study Details

Study Description

Brief Summary

So far, therapies have limited success in functional recovery in adults with chronic SCI. By introducing remote cognitive multisensory rehabilitation (CMR), which has shown significant functional improvements due to neurological recovery when delivered in-person, transformative results that (i) provide a potentially effective new therapy within the healthcare system, accessible to more patients, and (ii) demonstrate brain function changes alongside improved function in chronic SCI are anticipated. The results will inform and justify a large scale federally funded clinical trial.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Remote CMR
  • Behavioral: Remote Exercise
Phase 2

Study Design

Study Type:
Interventional
Anticipated Enrollment :
22 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Remotely Delivered Cognitive Multisensory Rehabilitation for Sensory and Motor Recovery After Spinal Cord Injury
Anticipated Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2025
Anticipated Study Completion Date :
Jun 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Remote CMR

adults with SCI without restriction for race, sex or socio-economic status randomized to CMR intervention.

Behavioral: Remote CMR
12 weeks of remote CMR is done 3x/week, 45 min/session.

Placebo Comparator: Remote exercises

adults with SCI without restriction for race, sex or socio-economic status randomized to remote exercise intervention.

Behavioral: Remote Exercise
12 weeks of remote exercise is done 3x/week, 45 min/session.

Outcome Measures

Primary Outcome Measures

  1. International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI) Neurologic Exam [baseline]

    a clinical test originally designed to describe the extent and severity of a patient's SCI/D

  2. International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI) Neurologic Exam [12 weeks]

    a clinical test originally designed to describe the extent and severity of a patient's SCI/D

  3. the Neuromuscular Recovery Scale (NRS) [baseline]

    includes 11 items focused on the capacity of the trunk and lower extremity muscles to perform tasks such as sit, trunk extension, sit to stand, walking, and step retraining. The NRS provides a functional recovery measure that focuses on non-compensatory recovery.

  4. the Neuromuscular Recovery Scale (NRS) [12 weeks]

    includes 11 items focused on the capacity of the trunk and lower extremity muscles to perform tasks such as sit, trunk extension, sit to stand, walking, and step retraining. The NRS provides a functional recovery measure that focuses on non-compensatory recovery.

  5. The SCI-FI/AT [baseline]

    (32 items) reliably measures function in the domains of basic mobility, self-care, fine motor function, and ambulation.

  6. The SCI-FI/AT [12 weeks]

    (32 items) reliably measures function in the domains of basic mobility, self-care, fine motor function, and ambulation.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 18-75 years old, with an incomplete or complete SCI/D of ≥ 3months, medically stable.

  • be recruited from Hospitals within the Minnesota Regional Spinal Cord Injury Model System (MN Regional SCIMS), HealthPartners Neuroscience Center, Minneapolis VA Healthcare System, Duluth, and in the community.

Exclusion Criteria:
  • adults with MRI contra-indications (stabilizing hardware is typically MRI safe);

  • adults with uncontrolled seizure disorder;

  • adults with cognitive impairment and/or communicative disability (e.g., due to brain injury) that prevent them from following directions or from learning;

  • adults with with ventilator dependency;

  • adults with other major medical complications

  • pregnant women

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Minnesota Minneapolis Minnesota United States 55455

Sponsors and Collaborators

  • University of Minnesota

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Minnesota
ClinicalTrials.gov Identifier:
NCT05870189
Other Study ID Numbers:
  • CMR
First Posted:
May 23, 2023
Last Update Posted:
May 23, 2023
Last Verified:
May 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 23, 2023