Remotely Delivered Cognitive Multisensory Rehabilitation for Sensory and Motor Recovery After Spinal Cord Injury
NCT ID: NCT05870189
Last Updated: 2025-07-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
19 participants
INTERVENTIONAL
2023-06-01
2025-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Remote CMR
adults with SCI without restriction for race, sex or socio-economic status randomized to CMR intervention.
Remote CMR
12 weeks of remote CMR is done 3x/week, 45 min/session.
Remote exercises
adults with SCI without restriction for race, sex or socio-economic status randomized to remote exercise intervention.
Remote Exercise
12 weeks of remote exercise is done 3x/week, 45 min/session.
Interventions
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Remote CMR
12 weeks of remote CMR is done 3x/week, 45 min/session.
Remote Exercise
12 weeks of remote exercise is done 3x/week, 45 min/session.
Eligibility Criteria
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Inclusion Criteria
* 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 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
18 Years
75 Years
ALL
No
Sponsors
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University of Minnesota
OTHER
Responsible Party
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Locations
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University of Minnesota
Minneapolis, Minnesota, United States
Countries
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Other Identifiers
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CMR
Identifier Type: -
Identifier Source: org_study_id
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