Remote cognitive rehabilitation for recovery after spinal cord injury
Remotely Delivered Cognitive Multisensory Rehabilitation for Sensory and Motor Recovery After Spinal Cord Injury
PHASE2 · University of Minnesota · NCT05870189
This study tests whether a new remote therapy can help people with spinal cord injuries improve their thinking skills and recover better.
Quick facts
| Phase | PHASE2 |
|---|---|
| Study type | Interventional |
| Enrollment | 22 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | University of Minnesota (other) |
| Locations | 1 site (Minneapolis, Minnesota) |
| Trial ID | NCT05870189 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of remotely delivered cognitive multisensory rehabilitation (CMR) for individuals with spinal cord injuries (SCI). It aims to assess whether this innovative approach can lead to significant functional improvements and neurological recovery in patients who have experienced chronic SCI. By utilizing remote delivery methods, the study seeks to make this therapy more accessible to a larger patient population. The findings will also provide insights into brain function changes associated with improved recovery outcomes.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-75 with either complete or incomplete spinal cord injuries that have persisted for at least three months.
Not a fit: Patients with uncontrolled seizure disorders, significant cognitive impairments, or other major medical complications may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could offer a new, accessible therapy option that significantly enhances recovery for patients with spinal cord injuries.
How similar studies have performed: While traditional in-person CMR has shown promise, the remote delivery approach is relatively novel and has not been extensively tested in this context.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Minneapolis, Minnesota
- University of Minnesota — Minneapolis, Minnesota, United States (RECRUITING)
Study contacts
- Study coordinator: Ann Van de Winckel, PhD,MSPT,PT
- Email: avandewi@umn.edu
- Phone: 612-625-1191
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Spinal Cord Injuries, Spinal Cord Diseases