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AmputationNCT06182202

Comparing Intact and Residual Amputated Muscle

A study testing Powered Prosthesis in people with Amputation, run by North Carolina State University at 1 site in United States.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Lower limb amputees rely on their prosthetic to remain active and lead an independent life. In recent years, measuring residual muscle activity has been used to interpret a user's intent and thereby modulate prosthesis control. Read more about this study

Who is it for?
Ages 18 to 64 yearsHealthy volunteers can take part
Conditions the study is for
Amputation
What is being tested?
Powered Prosthesis
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
80 participants
Where
1 siteUnited States
Study dates
17 Jun 2022to 31 May 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 64 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Live in the United States
  • 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

Who cannot join

  • Have any cognitive, visual, or balance impairments that affects your ability to provide informed consent or to follow instructions during the experiments
  • 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
Show all 15Show fewer
  • 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

Trial locations and contacts

1 site in 1 country.

Ming Liu, PhD contact

919-515-8541

mliu10@ncsu.edu

Noah Rubin, BA contact

nrubin@ncsu.edu

United States1 site, 1 recruiting
  • North Carolina State University

    Raleigh, North Carolina, 27695

    He Huang, PhD, 919-515-5218, hhuang11@ncsu.edu

    Laura Rohrbaugh, 919-513-3840, lasmith6@ncsu.edu

    Recruiting

Other trials in United States

About this study

Official title: Comparing Intact and Residual Amputated Neuromuscular Physiology

Lower limb amputees rely on their prosthetic to remain active and lead an independent life. In recent years, measuring residual muscle activity has been used to interpret a user's intent and thereby modulate prosthesis control. However, little knowledge is held on how residual muscle activity differs from non-amputated muscle. The research team will analyze and compare neuromuscular physiology in non-amputee individuals and amputees' non-amputated and residual muscles across functional tasks to better understand how amputees control their muscles. Such information will inform design of modern prosthesis controllers.

Read the detailed description

There will be approximately 80 participants in this study: 40 who have lower-limb amputations and 40 who do not.

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):
  2. Muscle Activity Sensors: i. Number: 4 ii. Placement: 1 on the front and back of the leg below the knee.
  3. Muscle Activation While Sitting (Sessions 2-3):
  4. 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.
  5. Muscle shape sensors: i. Number: 2 ultrasound probes ii. Placement: On the front and back of their leg, switching legs between sessions.
  6. Prosthesis Fitting (Sessions 4-6):
  7. 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.
  8. Powered Prosthesis Device i. A trained prosthetist will assist aligning the casted socket with a powered prosthesis the research team have in the lab.
  9. Functional Tasks (Sessions 7-16):
  10. 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).
  11. 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:
  2. 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.
  3. The research team will provide them with visual biosignal feedback to guide them how to control their muscles.
  4. 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.
  5. 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:
  6. Quiet standing (not moving)
  7. Postural sway (leaning forward and backward)
  8. Sitting down and standing up repeatedly
  9. Squatting
  10. Standing up on toes (heel-raises)
  11. 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
Amputation
Being tested
Powered Prosthesis
Keywords
Amputees, Electromyography, Ultrasound, Neuromuscular Physiology, Prostheses, Muscle Activation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Powered ProsthesisDevice

    Custom in-house powered prosthetic device (used in prior studies, see Citations).

Study groups in NCT06182202
Study groupRoleWhat they receive
Individuals Without AmputationNo interventionNo Intervention Tested in identical tasks for comparison to Individuals with Amputation
Individuals With AmputationExperimentalTasks with a passive prosthesis Tasks with a powered active prosthesis
Receives: Device: Powered Prosthesis

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Motor Unit Action Potential Amplitudes

    The investigators will measure muscle activity via electromyography on the individuals' muscles controlling their ankle joint (note for residual muscle they are controlling their phantom limb).

    Properties of motor units will be gathered from surface electromyography (EMG) decomposed into individual motor unit firings.

    These properties will be compared between intact and residual muscle.

    Measured: Through study completion (an average of 36 months).

  2. Motor Unit Coherence

    The investigators will measure muscle activity via electromyography on the individuals' muscles controlling their ankle joint (note for residual muscle they are controlling their phantom limb).

    Properties of motor units will be gathered from surface electromyography (EMG) decomposed into individual motor unit firings.

    These properties will be compared between intact and residual muscle.

    Measured: Through study completion (an average of 36 months).

Secondary outcomes (1)
  1. Muscle Architecture Properties -- Muscle Volume

    The investigators will measure muscle architecture via ultrasound on the individuals' muscles controlling their ankle joint.

    Properties of architecture will be compared between residual muscle and intact muscle of both participant groups.

    Measured: Through study completion (an average of 36 months).

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Dec 2023
  2. Study start17 Jun 2022
  3. Primary completion31 Dec 2024 (estimated)
  4. Study completion31 May 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Crossover
Masking
None (open label)
Enrolment
80 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06182202
Sponsor's protocol ID
24436
Status last verified
Dec 2023
First submitted
8 Jul 2022
Last updated
26 Dec 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
No

Publications

  • 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.

    PubMed 26057851

Questions about this trial

What is this clinical trial studying?

A study testing Powered Prosthesis in people with Amputation, run by North Carolina State University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 15 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 26 Dec 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Ming Liu, PhD (919-515-8541, mliu10@ncsu.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Motor Unit Action Potential Amplitudes (time frame: Through study completion (an average of 36 months).). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06182202, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Dec 2023.

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Comparing Intact and Residual Amputated Muscle | AzTrials