Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Amputation
  • Prosthesis
  • Prosthesis User
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: Two-group study with same baseline and intervention. One group ceases intervention and returns to control condition.Masking: None (Open Label)Primary Purpose: Device Feasibility

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Participants will undergo informed consent and schedule an initial site visit. A logging device will be used to track activity of prosthetic arm usage while in everyday use at home. After a baseline period, participants will schedule a second visit to be introduced to the training technology. The st...

Participants will undergo informed consent and schedule an initial site visit. A logging device will be used to track activity of prosthetic arm usage while in everyday use at home. After a baseline period, participants will schedule a second visit to be introduced to the training technology. The study will span up to 7 months with participants training at home for 15-60 minutes, 3-5 times a day. Every 3-6 weeks, investigators will schedule a study event and sit visit to conduct functional outcome tasks and measurements.

Tracking Information

NCT #
NCT04354493
Collaborators
Not Provided
Investigators
Not Provided