Actively Recruiting
Spinal Cord Injury Neurorecovery Collaboration
Led by University of Melbourne · Updated on 2025-08-08
24
Participants Needed
1
Research Sites
147 weeks
Total Duration
On this page
Sponsors
U
University of Melbourne
Lead Sponsor
I
Institute of Breathing and Sleep
Collaborating Sponsor
AI-Summary
What this Trial Is About
SCINC is an adaptive design Master protocol that seeks to determine if there is "sufficient promise" of beneficial effect of treatment combinations to enhance motor recovery in pre-specified strata of people with a spinal cord injury.
CONDITIONS
Official Title
Spinal Cord Injury Neurorecovery Collaboration
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Person with spinal cord injury
- Adults older than 18 years
- Able to breathe independently
- Chronic spinal cord injury more than 1 year after injury or impairment onset
- Tetraplegia with injury level between C2 and T1
- Evidence of some movement in the upper limb below the injury level
- Have a documented plan to manage Autonomic Dysreflexia if it occurs
You will not qualify if you...
- Proven contraindication to the intervention
- Pregnancy
- Medical instability including current or recent infection or inflammation within 6 weeks
- Current or recent pressure ulcers or skin lesions within 6 weeks
- Poorly controlled diabetes
- Autonomic Dysreflexia episode in the past 6 months requiring medical treatment
- Significant other neurological, psychiatric, lung, heart, bone, or cancer conditions
- Currently participating in another clinical trial
- Upper limb contracture
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Austin Health
Heidelberg, Victoria, Australia, 3084
Actively Recruiting
Research Team
L
Laura Stendell
CONTACT
N
Nicole Sheers, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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