Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:27 AM
Ignite Modification Date:
2025-12-25 @ 2:27 AM
NCT ID:
NCT07299734
Eligibility Criteria:
Inclusion Criteria:
* Chronic cervical SCI
* Any level or severity of cervical SCI, traumatic or non-traumatic
* Can carry out object manipulations but with visible impairment (i.e., 5-25 on the GRASSP Prehension Performance sub-score).
Exclusion Criteria:
* Any disease or injury other than the SCI that may be affecting grasping performance.
* Individuals with any self-reported FES contraindications (pacemakers, implantable defibrillator, implanted neurostimulation device, metallic implants in the stimulated areas, cardiac conditions, epilepsy, uncontrolled seizures, wounds or fractures on the target limb)
* Inability to understand the study procedures
* Muscles do not respond to FES to produce grasping movements
* Currently participating in another upper limb rehabilitation intervention study (regular physical and occupational therapy is permitted).
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT07299734
Study Brief:
Protocol Section:
NCT07299734