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

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

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05870189
Enrollment
19
Registered
2023-05-23
Start date
2023-06-01
Completion date
2025-06-30
Last updated
2025-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal Cord Diseases, Spinal Cord Injuries

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.

Interventions

BEHAVIORALRemote CMR

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

BEHAVIORALRemote Exercise

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

Sponsors

University of Minnesota
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
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

Design outcomes

Primary

MeasureTime frameDescription
International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI) Neurologic Exambaselinea clinical test originally designed to describe the extent and severity of a patient's SCI/D
the Neuromuscular Recovery Scale (NRS)baselineincludes 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.
The SCI-FI/ATbaseline(32 items) reliably measures function in the domains of basic mobility, self-care, fine motor function, and ambulation.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 11, 2026