Ignite Creation Date:
2024-05-06 @ 3:07 PM
Last Modification Date:
2024-10-26 @ 1:43 PM
Study NCT ID:
NCT04523636
Status:
COMPLETED
Last Update Posted:
2020-08-21
First Post:
2020-08-18
Brief Title:
Evaluation of Splinting in Tetraplegia
Sponsor:
Thomas Jefferson University
Organization:
Thomas Jefferson University
Study Overview
Official Title:
Evaluation of Splinting in Tetraplegia
Status:
COMPLETED
Status Verified Date:
2020-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study compared pre-fabricated and custom resting hand splints among people who were in inpatient rehabilitation after a cervical spinal cord injury
Detailed Description:
This was randomized parallel group controlled clinical trial where arms not patients were the unit of randomization This trial was funded by the Craig H Neilsen Allied Health Professional Development Award of the American Spinal Injury Association ASIA This research was conducted at a 32-bed spinal cord injury and multi-trauma rehabilitation unit in an urban center Participants were recruited from an inpatient spinal cord injury rehabilitation unit Eligible participants were 18 years or older and undergoing acute rehabilitation after a cervical spinal cord injury with hand function impairment and the primary occupational therapist deemed splinting intervention was required Each eligible extremity was randomized to receive a custom or pre-fabricated resting hand splint for night use
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None