COMPLETED

Assessment of Gesture Accuracy of a Prosthesis Control System

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The study is evaluating the performance of prosthesis control system, referred to as Phantom X, in able bodied individuals and individuals with upper limb amputation at the forearm level.

Official Title

Assessment of Gesture Accuracy for a Multi-electrode EMG Sensor Array Based Prosthesis Control System

Quick Facts

Study Start:2024-08-13
Study Completion:2025-04-18
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06446037

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:21 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Individuals 21 years in age and older
  2. 2. Individuals with amputation of one or both arms at transradial level (applies to amputees only)
  3. 3. Ability to follow study directions
  4. 4. Willingness and ability to sign Informed Consent
  1. 1. Individuals with previously diagnosed muscle pathologies
  2. 2. Individuals with impaired muscle function and/or impaired ability to perform normal hand movements (normal participants) or ability to perform normal phantom hand movements (amputees)
  3. 3. Individuals with transhumeral or higher amputation of both arms (applies to amputees only)
  4. 4. Cognitively impaired to follow study instructions
  5. 5. Allergies to skin adhesive materials necessary for cutaneous electrode placement
  6. 6. Excessive hair growth on arms and inability to shave off the hair for electrode placement
  7. 7. Pregnant woman
  8. 8. Arms or residual limbs with insufficient diameter to accommodate the wearing of two cutaneous sensor arrays
  9. 9. Injuries, bruises, or open wounds on the arm that needs to be instrumented for the study

Contacts and Locations

Study Locations (Sites)

Phantom Neuro Inc. Operational Headquarters
Austin, Texas, 78704
United States

Collaborators and Investigators

Sponsor: Phantom Neuro Inc.

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-08-13
Study Completion Date2025-04-18

Study Record Updates

Study Start Date2024-08-13
Study Completion Date2025-04-18

Terms related to this study

Keywords Provided by Researchers

  • Prosthesis
  • Upper limb amputee

Additional Relevant MeSH Terms

  • Upper Limb Amputation Below Elbow (Injury)