MSPT Device Usability Study
Completed
Conditions studied: Multiple Sclerosis
In brief
The primary objective of this feasibility study is to evaluate the functionality (e.g., as defined by the primary endpoints) of the fully integrated Multiple Sclerosis Performance Test (MSPT) device, when used by unsupervised participants with MS, or related conditions, with a broad range of disability, in multi-clinical-care environments. Secondary objectives include: Participant perception of usability of device; Participant satisfaction with the device; Ascertain the impact of different clinical environments on device usability; Ascertain impact of assistive devices in usability of device; Ascertain functionality of Bluetooth remote as compared with manual timing.
Key facts
- Study ID
- NCT02664324
- Run by
- Biogen
- People needed
- 60
- Starts
- 2016-03-01
- Expected to finish
- 2016-04-01
- Last updated by the study team
- 2016-05-04
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Research Site — Baltimore, Maryland, United States
- Research Site — New York, New York, United States
- Research Site — Cleveland, Ohio, United States
Full record on ClinicalTrials.gov
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