This feasibility and non-randomized comparison study explores the possible benefits of splint design and production by 3D-printing in a clinical setting and looks at splint users' experiences with customizable 3D-printed finger splints compared to conventionally made splints. Fifty participants with a hyperextended finger condition are assigned by researcher to either an interventional group (customizable 3D-printed finger splint) or a control group (conventional thermoplastic finger splint). Participants will wear assigned splint for 1 month. Functional status and satisfaction with splint will be assessed at the end of the 1-month duration in the form of surveys on satisfaction and functional status participants will be asked to complete. The findings will contribute to evidence that customizable 3D-printed finger splints can serve as a feasible, cost-effective option to improve patient satisfaction and functional status. It will further justify the need for the application of 3D-printing in a clinical setting.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
SCREENING
Masking
SINGLE
Enrollment
22
The intervention is wearing a novel finger splint produced by a 3D-printer
This intervention is wearing a finger splint produced by a conventional method using thermoplastic material typically used in a clinical setting
Swedish Hospital Part of NorthShore University HealthSystems
Chicago, Illinois, United States
NorthShore University HealthSystem
Evanston, Illinois, United States
Modified Version of Orthotics and Prosthetics User Survey - Satisfaction with Device
A modified version of a Self-report questionnaire which measures participants satisfaction with assigned splint device
Time frame: 1 month
Modified Version of Orthotics and Prosthetics User Survey - Functional Status
A modified version of a Self-report questionnaire which measures participants' functional status during the duration of time wearing assigned finger splint device
Time frame: 1 month
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