tSCS + UL Robotics Training in SCI Patients
Recruiting
N/A
Interventional Study
Spinal Cord Injuries
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 21 – 80
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 6 (estimated)
- Sponsor
- National University Hospital, Singapore · Other
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About This Trial
This study is aimed to evaluate whether transcutaneous spinal cord stimulation (tSCS) can augment upper limb robotic training (ULRT) to improve functional mobility in participants with chronic spinal cord injuries. It also evaluates the impact of the tSCS+ULRT on health-related quality of life (HRQOL), compared to ULRT alone.
This is a prospective single-arm crossover study in participants with i…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. At least 6 months to 5 years from the diagnosis of the traumatic SCI;
2. Participants between 21 and 80 years of age;
3. C2-8 level injuries;
4. ISNCSCI-UEMS \>25,
5. Pinch force \> 25 N;
6. Grasp force \> 100 N;
7. Able to perform the box and block test;
8. Sitting tolerance…
Contacts