The objective of this study is to evaluate the efficacy of the Point Powered system as compared to the patient's standard-of-care treatment. This study will be a single subject crossover design where one group of 10 adult partial hand amputees will be evaluated on several metrics on their existing prosthetic treatment (Treatment 1) and the Point Powered system (Treatment 2) over a period of three months using standard two-site myoelectric control. Metrics include: in-clinic functional measures, subjective assessments, bilateral hand use, and prosthesis wear time.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Assessment of Capacity for Myoelectric Control (ACMC)
Timeframe: Baseline (pre-fitting)
The Southampton Hand Assessment Procedure (SHAP)
Timeframe: Baseline (pre-fitting)
PROMIS Social Isolation
Timeframe: Baseline (pre-fitting)
PROMIS Ability to Participate
Timeframe: Baseline (pre-fitting)
PROMIS Physical Function - Upper Extremity
Timeframe: Baseline (pre-fitting)
PROMIS Satisfaction with Social Roles and Activities
Timeframe: Baseline (pre-fitting)
Assessment of Capacity for Myoelectric Control (ACMC)
Timeframe: Immediately post-fitting
The Southampton Hand Assessment Procedure (SHAP)
Timeframe: Immediately post-fitting
PROMIS Social Isolation
Timeframe: Immediately post-fitting
PROMIS Ability to Participate
Timeframe: Immediately post-fitting
PROMIS Physical Function - Upper Extremity
Timeframe: Immediately post-fitting
PROMIS Satisfaction with Social Roles and Activities
Timeframe: Immediately post-fitting
Assessment of Capacity for Myoelectric Control (ACMC)
Timeframe: 30 days post-fitting
The Southampton Hand Assessment Procedure (SHAP)
Timeframe: 30 days post-fitting
PROMIS Social Isolation
Timeframe: 30 days post-fitting
PROMIS Ability to Participate
Timeframe: 30 days post-fitting
PROMIS Physical Function - Upper Extremity
Timeframe: 30 days post-fitting
PROMIS Satisfaction with Social Roles and Activities
Timeframe: 30 days post-fitting
Assessment of Capacity for Myoelectric Control (ACMC)
Timeframe: 60 days post-fitting
The Southampton Hand Assessment Procedure (SHAP)
Timeframe: 60 days post-fitting
PROMIS Social Isolation
Timeframe: 60 days post-fitting
PROMIS Ability to Participate
Timeframe: 60 days post-fitting
PROMIS Physical Function - Upper Extremity
Timeframe: 60 days post-fitting
PROMIS Satisfaction with Social Roles and Activities
Timeframe: 60 days post-fitting