Spinal Cord Injuries
Conditions
Keywords
Spinal Cord Injuries, spinal cord injury
Brief summary
The percentages of participants in clinical studies haven't always been perfectly representative of a particular group. This research examines the variables that affect a patient's choice to enroll in, discontinue participation in, or resume participation in a clinical trial for spinal cord injury. It will also try to analyze data from the perspective of different demographic groups to check for recurring trends which might yield insights for the sake of future spinal cord injury research.
Interventions
None listed
Sponsors
Power Life Sciences Inc.
Study design
Observational model
CASE_CROSSOVER
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Aged ≥ 18 years old * Ability to understand and the willingness to sign a written informed consent document. * Diagnosis of spinal cord injury
Exclusion criteria
* Is pregnant, breastfeeding or expecting to conceive within the projected duration of the study * Has a serious medical or psychiatric illness likely to interfere with participation in this clinical study. * Inability to provide written informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rate of patients who decide to enroll in a spinal cord injury clinical study. | 3 months |
| Number of spinal cord injury study participants who remain in clinical trial until completion. | 12 months |
Contacts
Primary ContactMichael B Gill
Outcome results
None listed