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 @ 3:28 AM
Ignite Modification Date:
2025-12-25 @ 3:28 AM
NCT ID:
NCT06989905
Eligibility Criteria:
Inclusion Criteria:
* Adult (≥18 yrs old)
* A history of injury to spinal cord at or above C6
* \>6 months post SCI
* Weak wrist extension at least unilaterally
* Expectation that current medication will be maintained without change for at least 3 months. Stable use of anti-spasticity medication (e.g., baclofen, diazepam, tizanidine) is accepted.
Exclusion Criteria:
* Motoneuron injury
* Medically unstable condition
* Cognitive impairment
* A history of epileptic seizures
* Metal implants in the cranium
* Implanted biomedical device in or above the chest (e.g., a cardiac pacemaker, cochlear implant)
* Extensive use of functional electrical stimulation to the arm on a daily basis
* Pregnancy (due to changes in posture and potential medical instability)
* Contraindications to MRI
* No measurable MEP elicited in the ECR
* Unable to produce any voluntary ECR EMG activity
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06989905
Study Brief:
Protocol Section:
NCT06989905