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.
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.
Noah Rubin, BA contact
United States1 site, 1 recruiting
- 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
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.
- Muscle Activation While Sitting (Session 1):
- Muscle Activity Sensors: i. Number: 4 ii. Placement: 1 on the front and back of the leg below the knee.
- Muscle Activation While Sitting (Sessions 2-3):
- 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.
- Muscle shape sensors: i. Number: 2 ultrasound probes ii. Placement: On the front and back of their leg, switching legs between sessions.
- Prosthesis Fitting (Sessions 4-6):
- 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.
- Powered Prosthesis Device i. A trained prosthetist will assist aligning the casted socket with a powered prosthesis the research team have in the lab.
- Functional Tasks (Sessions 7-16):
- 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).
- 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:
- Muscle Activation While Sitting (Sessions 1-3): Come to the lab for 3 initial sessions, where they will:
- 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.
- The research team will provide them with visual biosignal feedback to guide them how to control their muscles.
- 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.
- 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:
- Quiet standing (not moving)
- Postural sway (leaning forward and backward)
- Sitting down and standing up repeatedly
- Squatting
- Standing up on toes (heel-raises)
- 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 group | Role | What they receive |
|---|---|---|
| Individuals Without Amputation | No intervention | No Intervention Tested in identical tasks for comparison to Individuals with Amputation |
| Individuals With Amputation | Experimental | Tasks 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.
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).
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)
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.
- First posted26 Dec 2023
- Study start17 Jun 2022
- Primary completion31 Dec 2024 (estimated)
- Study completion31 May 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for AmputationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- North Carolina State University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, He Huang, North Carolina State University
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
Study at a glance
From the registry record, last updated by the sponsor on 26 Dec 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparing Intact and Residual Amputated Neuromuscular Physiology
- ClinicalTrials.gov ID
- NCT06182202
- Acronym / sponsor ID
- 24436
- Conditions
- Amputation
- Keywords
- Amputees, Electromyography, Ultrasound, Neuromuscular Physiology, Prostheses, Muscle Activation
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 80 participants (estimated)
- Lead sponsor
- North Carolina State UniversityUniversity, hospital or other
- Study start
- 17 Jun 2022 (actual)
- Primary completion
- 31 Dec 2024 (estimated)
- Study completion
- 31 May 2025 (estimated)
- First posted
- 26 Dec 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
- Muscle Activation While Sitting (Session 1):
- Muscle Activity Sensors: i. Number: 4 ii. Placement: 1 on the front and back of the leg below the knee.
- Muscle Activation While Sitting (Sessions 2-3):
- 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.
- Muscle shape sensors: i. Number: 2 ultrasound probes ii. Placement: On the front and back of their leg, switching legs between sessions.
- Prosthesis Fitting (Sessions 4-6):
- 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.
- Powered Prosthesis Device i. A trained prosthetist will assist aligning the casted socket with a powered prosthesis the research team have in the lab.
- Functional Tasks (Sessions 7-16):
- 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).
- 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:
- Muscle Activation While Sitting (Sessions 1-3): Come to the lab for 3 initial sessions, where they will:
- 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.
- The research team will provide them with visual biosignal feedback to guide them how to control their muscles.
- 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.
- 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:
- Quiet standing (not moving)
- Postural sway (leaning forward and backward)
- Sitting down and standing up repeatedly
- Squatting
- Standing up on toes (heel-raises)
- 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.
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Individuals Without Amputation | No intervention | –No Intervention Tested in identical tasks for comparison to Individuals with Amputation |
| Individuals With Amputation | Experimental | Device: Powered ProsthesisTasks with a passive prosthesis Tasks with a powered active prosthesis |
Who may qualify
- Ages
- 18 to 64 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (7 listed)
- 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
Key exclusion criteria (15 listed)
- 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)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Powered ProsthesisCustom in-house powered prosthetic device (used in prior studies, see Citations). | Device | Individuals With Amputation |
Primary outcome
Motor Unit Action Potential Amplitudes
Time frame: Through study completion (an average of 36 months).
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.
Motor Unit Coherence
Time frame: Through study completion (an average of 36 months).
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.
1 secondary outcome
Muscle Architecture Properties -- Muscle Volume
Time frame: Through study completion (an average of 36 months).
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Dec 2023.
- Background: PubMed 26057851Huang 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.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Noah Rubin, BA contact
1 site in 1 country: see every site and its status.
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.