Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
80 participants
INTERVENTIONAL
2022-06-17
2025-05-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
A minimum of 48 hours will separate each testing session.
A warm-up is incorporated into every session and subjects will regularly take breaks between trials. The research team will check in with them regularly, and they are welcome to tell us when they want a break or stop at any time for any reason.
Subjects will be asked to conducted controlled isolated muscle activity of their ankle muscles, given feedback of their muscle activation to control their effort and prevent fatigue. Following activity of isolated muscles, subjects will be asked to conduct functional tasks including quiet standing, postural sways, sitting down and standing up, squats, heel-raises, and walking.
Individuals with amputation will conduct the tasks with their personal passive prosthesis device as well as a powered active prosthesis (following socket fitting and appropriate adjustment to comfort by a certified, trained prosthetist) to compare muscle activity in functional tasks. Individuals without amputation will conduct the tasks for further comparison.
Surface electromyography, ultrasound, and motion capture data will be used to record muscle activation, muscle architecture, and joint biomechanics respectively and evaluate observations and effects between residual and intact muscles.
More details are below.
\-- The following sensors/devices will be attached for the study. The sensors will be fixed via a double-sided adhesive, self-adhesive wraps, or straps. All are easily removable and adjustable for their comfort. Wearing shorts is recommended to simplify the process of adding sensors.
1. Muscle Activation While Sitting (Session 1):
a. Muscle Activity Sensors: i. Number: 4 ii. Placement: 1 on the front and back of the leg below the knee.
2. Muscle Activation While Sitting (Sessions 2-3):
a. Muscle Activity Sensors: i. Same as Session 1 b. Joint Dynamics Device: i. Subjects' on-amputated foot will be strapped into a platform that measures how much they are pulling/pushing or moving their ankle. On tasks thinking about activating the phantom limb, the research team will ask participants to match activities with both limbs so that the research team can record what the participants are thinking about with the phantom limb via the non-amputated foot.
c. Muscle shape sensors: i. Number: 2 ultrasound probes ii. Placement: On the front and back of their leg, switching legs between sessions.
3. Prosthesis Fitting (Sessions 4-6):
a. Muscle Activity Sensors: i. Same as Session 1 b. Socket: i. A trained prosthetist will cast and fit a socket designed to safely fit the muscle activity sensors.
c. Powered Prosthesis Device i. A trained prosthetist will assist aligning the casted socket with a powered prosthesis the research team have in the lab.
4. Functional Tasks (Sessions 7-16):
a. Muscle Activity Sensors: i. Number: 18 ii. Placement: 1 on the front and back of the leg below the knee, 2 on the front of the leg above the knee, 1 on the back of the leg below the knee (5 per leg), 2 on the arm above and below the elbow (4 per arm) b. Socket: i. Fitted in earlier sessions c. Powered Prosthesis Device i. Fitted and aligned in earlier sessions d. Movement measurement markers: i. Number: 40 in total. ii. Placement: 4 on head, 5 on torso, 7 on each arm, 5 on hips, 3 on each leg, 1 on each ankle, toes and heels (on the shoe).
e. Harness: i. A harness attached to the ceiling will be used to catch subjects case of any fall during the experiment.
During each visit the research team will ask subjects to do all the following:
1. Muscle Activation While Sitting (Sessions 1-3): Come to the lab for 3 initial sessions, where they will:
1. Practice muscle activation of their ankle muscles while wearing sensors measuring their muscle activity and shape. There will be a brief calibration to their maximum effort to ensure muscle activation will be less than maximum effort throughout the rest of the study.
2. The research team will provide them with visual biosignal feedback to guide them how to control their muscles.
2. Prosthesis Fitting (Sessions 4-6): Attend a session where a trained prosthetist will cast their residual limb for a socket, followed by 1, 2, or 3 fitting (up to 3 total) sessions with their socket and a powered prosthesis with a certified prosthetist. Each visit will last up to two hours. The prosthetist will duplicate their current socket and ask them to wear it with a powered prosthesis. The prosthetist will also conduct modifications if they do not like the socket to ensure fit and their comfort while wearing the socket.
3. Functional Tasks (Sessions 7-16): Once the fit has been finalized, the participants will come to the lab for up to 10 additional sessions for functional tasks. During each visit, the participants will be asked to practice modulating and controlling the activation of the amputated and non-amputated muscles. After training and practicing activating and controlling the muscles, the research team will then ask the participants to conduct the following tasks:
1. Quiet standing (not moving)
2. Postural sway (leaning forward and backward)
3. Sitting down and standing up repeatedly
4. Squatting
5. Standing up on toes (heel-raises)
6. Walking on a treadmill at their preferred walking speed
Handrails (both left and right) will be always available to allow balance support if needed, and additional harness protection is available.
Individuals without amputation will conduct the functional tasks set once. Individuals with amputation will be asked to do the functional task set both with their passive prosthesis and a powered prosthesis to determine if the powered device improves functional performance, in addition to compare to individuals without amputation. At times, the research team will give them auditory feedback to help the participants time the motion, and visual biosignal feedback to guide them on how the participants place the weight between legs.
The research team expect the participants to come in for up to additional 10 sessions for these activities to account for adaptations in performance when using a powered prosthesis, and post-training evaluations of their amputated and non-amputated muscles. This estimate also accommodates necessary setup and take-down time that subjects must be present for, while maintaining reasonable individual session periods.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NON_RANDOMIZED
CROSSOVER
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Individuals Without Amputation
No Intervention Tested in identical tasks for comparison to Individuals with Amputation
No interventions assigned to this group
Individuals With Amputation
Tasks with a passive prosthesis Tasks with a powered active prosthesis
Powered Prosthesis
Custom in-house powered prosthetic device (used in prior studies, see Citations).
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Powered Prosthesis
Custom in-house powered prosthetic device (used in prior studies, see Citations).
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Are 18 years of age or older
* Can walk across low-level environmental barriers such as curbs, stairs, or uneven surfaces unassisted and without much difficulty
* Live in the United States
* Are a unilateral lower-limb amputee
* Have lower limb length from the knee to where the amputation occurred at least 10cm long
* Can walk across low-level environmental barriers such as curbs, stairs, or uneven surfaces unassisted and without much difficulty
Exclusion Criteria
* Have had a stroke
* Have heart disease
* Weigh 450 pounds or more (for harness safety)
* Have a girth/waist circumference more than 49 inches (124.4 cm) (for harness safety)
* Have allergies to adhesives
\- Have any cognitive, visual, or balance impairments that affects your ability to provide consent or to follow instructions during the experiments
* Have had a stroke
* Have heart disease
* Had skin lesions/incomplete healing following amputation
* Have ulcers
* Have lower limb length from the knee to where the amputation occurred less than 10cm long
* Weigh 450 pounds or more (for harness safety)
* Have a girth/waist circumference more than 49 inches (124.4 cm) (for harness safety)
* Have allergies to adhesives
18 Years
64 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
North Carolina State University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
He Huang
Jackson Family Distinguished Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
North Carolina State University
Raleigh, North Carolina, United States
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
He Huang, PhD
Role: primary
Laura Rohrbaugh
Role: backup
References
Explore related publications, articles, or registry entries linked to this study.
Huang S, Wensman JP, Ferris DP. Locomotor Adaptation by Transtibial Amputees Walking With an Experimental Powered Prosthesis Under Continuous Myoelectric Control. IEEE Trans Neural Syst Rehabil Eng. 2016 May;24(5):573-81. doi: 10.1109/TNSRE.2015.2441061. Epub 2015 Jun 4.
Provided Documents
Download supplemental materials such as informed consent forms, study protocols, or participant manuals.
Document Type: Informed Consent Form
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
24436
Identifier Type: -
Identifier Source: org_study_id