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HealthyNCT04567797

Assessing the Efficacy of Passive Exoskeletons for Construction Work: Lab-Based Study

A study testing Laevo 2, backX and FLx ErgoSkeleton in people with Healthy, run by University of Arizona 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 The sponsor has not verified this record for over two years, so it may be out of date.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

This project aims to assess the effectiveness and acceptability of four types of commercial Back support exoskeletons (BSEs) for concrete work tasks. BSEs are external wearable devices designed to reduce physical demands on the back by providing assistive moments to body joints to support muscles. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Healthy
What is being tested?
Laevo 2, backX and FLx ErgoSkeleton
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
25 participants
Where
1 siteUnited States
Study dates
Oct 2020to Jan 2021
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 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Be at least 18 years old.
  • Be able to walk and/or lift heavy objects without pain/discomfort.

Who cannot join

  • Have prior back/neck injuries or chronic pain in the last 6 months.
  • Have a pacemakers.
  • Have breast implants.
  • Have removed the axillary lymph nodes.
  • Pregnant women.
  • Using blood thinning medications.
  • Participants must consult a physician prior to participating this study if any of the following occurred before or during use: Inguinal hernia, hernia, knee injury hip/knee prosthesis, hyperextended knee, recent surgery, skin disease/injury, scars, inflammation, skin reddening.

Trial locations and contacts

1 site in 1 country.

Sol Lim, Ph.D. contact

520-626-0728

lims@arizona.edu

Xiang Yang, Master contact

520-788-3880

xiangyang@email.arizona.edu

United States1 site
  • Smart Life in Motion (SLIM) Lab

    Tucson, Arizona, 85721

    Sol Lim, Ph.D., 520-626-0728, lims@arizona.edu

    Xiang Yang, Master, 520-788-3880, xiangyang@email.arizona.edu

Other trials in United States

About this study

This project aims to assess the effectiveness and acceptability of four types of commercial Back support exoskeletons (BSEs) for concrete work tasks. BSEs are external wearable devices designed to reduce physical demands on the back by providing assistive moments to body joints to support muscles. There is considerable evidence to suggest such exoskeletons reduce the risks of back injuries for workers performing repetitive tasks. However, since the effects of using BSEs in concrete work tasks are still unknown, evidence-based information regarding effectiveness, productivity impact, and safety risks is required to help industries adopt BSEs as an ergonomic intervention.

Read the detailed description

The experimental protocol will require approximately 3 hours of the participant's time. It will be comprised of six stages:

Stage I: Body Discomfort and Handedness Questionnaires First, the research team will administer an interview questionnaire to the participant to obtain information on participants' body pain/discomfort level and to determine the participant's hand dominance using the Edinburgh Handedness Inventory.

Stage II: Anthropometric body measurements and strength testing Several anthropometric body dimensions will be measured in the standing upright position using a standard tape measure and anthropometer. Body measurements will include standing height, shoulder height, waist to floor height, leg length, knee height, upper and lower arm length, foot length, and inter shoulder distance. Study participants' body weight will be measured using a standard weighing scale. Maximum power grip strength on both hands will be measured for 3 trials using a standard hand-held grip dynamometer.

Stage III: Fitting BSEs Four types of commercial BSEs (backX, Laevo 2, FLx ErgoSkeleton, V22 ErgoSkeleton) will be introduced to participants. Following manufacturers' instructions, participants will be allowed to test each device, fit the device to their body for comfort by using adjustable features (e.g., straps).

Stage IV: Optical motion capture marker, wearable inertial sensors, and surface electromyography (sEMG) sensor placement A commercial motion-capture system (Qualisys AB, Kvarnbergsgatan, Göteborg, Sweden) will be used to monitor and analyze body segment motion trajectories in a three-dimensional space. Several optical markers will be placed on anatomical landmarks of study participants including the head, shoulders, arms, hands, back, pelvis, legs, and feet. Hypo-allergenic double-sided tape will be used to attach the optical markers to the anatomical landmarks. Wearable inertial sensors will be attached using hypoallergenic double-sided tape at the low-back near the waist (S1), upper back (T6), sternum, upper arm (R, L), lower arm (R, L), thigh (R, L), and shank (R, L). Eight sEMG sensors will be placed on Descending Trapezius (TRP), Anterior Deltoid (AD), Iliocostalis Lumborum (ILL), Rectus Abdominis (RA), External Oblique (EO), Cervical Erector Spinae (CES), Latissimus Dorsi (LD), and Vastus Lateralis (VL) to measure muscle activation level while performing simulated work tasks, which are described in Stage VI.

Stage V: Maximum Voluntary Contraction (MVC) measurement for muscle activation While performing work tasks, muscle activation level varies between muscles and between subjects. A common way is to normalize myoelectric activities of each muscle for every participant by measuring isometric Maximal Voluntary Contraction (MVC). In this study, the investigators will measure 11 MVCs before the start of actual work tasks. Our MVC tests will be based on a study of trunk muscles. Before the MVC measurement, participants will be asked to warm up by 5 stretch exercises: (a) Stand upright with his feet shoulder-width apart. Place his hands on his buttocks for support. Look upwards and slowly lean backward. Keep his legs sturdy. (b) Stand upright with his feet shoulder-width apart. Place one hand on his buttocks for support. Look up and slowly lean backward. Reach over with his opposite hand. Rotate the upper body at the waist. (c) Kneel on one foot. Place his hands on his hips. Push hips forward. If necessary, hold on to something to keep balance. (d) Stand upright with his feet shoulder-width apart. Cross his arms and place his hands on shoulders. Slowly rotate his shoulders to one side. To increase the intensity of this stretch, use his hands to help rotate sideways. (e) Kneel on all fours. Support himself with one hand and reach towards his ankle with the other. Keep his back parallel to the ground. Keep the back straight, parallel to the ground, and his thigh in a vertical position. Distribute his weight evenly on both hands and knees. After the warm-up, the MVC testing will be performed, which includes (1) upper trunk flexion: subject will be in a sit-up posture positioned on a bench with the legs bent and feet strapped down with a belt. He then will attempt to flex the upper trunk in the sagittal plane while her thorax will be manually braced by the experimenter; (2) upper trunk twisting (R and L): In the same sitting supported position, the subject will attempt to twist the upper trunk in the horizontal plane while his thorax will be manually braced by the experimenter;(3) lower trunk flexion: subject will attempt to flex the lower trunk in the sagittal plane while he will be in a supine laying position, but with knees and hips both bent to approximately 90 degrees. His thorax will be strapped down with a belt and his legs will be manually braced by the experimenter; (4) lower trunk twisting (R and L): In the same lying and supported position, the subject will attempt to twist the lower trunk in the horizontal plane while his legs will be manually braced by the experimenter;(5) upper trunk bending (R and L): subject will attempt to side bend the upper trunk in the frontal plane while he will be in a side-lying position, with the knees bent and strapped with a belt, and thorax and arms will be manually braced by the experimenter; (6) lower trunk bending: subject will maintain a right and left side bridge position while maximally resisted downward pressure on the pelvis will be applied by the experimenter;(7) upper trunk extension: subject will be strapped in a prone position, with the torso horizontally cantilevered over the end of the bench (Biering-Sorensen position). He will then attempt to extend the upper trunk in the sagittal plane and retract the shoulders (squeezing the scapulae together) while manual resistance will be applied on the shoulders by the experimenter; (8) lower trunk extension: subject will attempt to extend the lower trunk and the hips against manual resistance when in a prone position, with the torso on the bench and the legs horizontally cantilevered over the end of the bench; (9) shoulder rotation and adduction (R and L): subject will attempt to adduct and internally rotate the shoulder against manual resistance with the shoulder abducted and elbow flexed, both to 90 degrees. In addition, two unresisted maximal abdominal contractions will be performed in standing; (10) maximal effort abdominal hollowing: subject will attempt to maximally activate the deep abdominal muscles while drawing in the lower abdomen; (11) maximal effort abdominal bracing: subject will attempt to maximally activate all the abdominal wall without any change in the position of the muscles. In all MVC testing, participants will be asked to exert their maximum force at a static posture (instructions will be given by our researcher) for every five seconds. For the first two seconds, they will be asked to ramp up to their maximum and maintain the force for the next three seconds. MVCs will be tested at least two times for each muscle group.

Stage VI: Data collection in simulated construction work tasks Postural data will be recorded from participants while performing six simulated concrete work tasks (i.e., shoveling, framing, carrying and lifting of construction materials, hammering, and tying rebars) at different intensities. The material they will be lifting, carrying, shoveling, and holding will not go over the safety limit of 30 lbs, as stated by NIOSH. Participants will perform the tasks with vs. without wearing different BSEs. Task trials will be video recorded for visual correspondence when analyzing motion capture and inertial sensor data. Participants will be given two minutes rest break between tasks and thirty seconds rest break between trials. The order of task conditions within each work task will be randomized.

  • Task 1: Shoveling and moving construction material from location A to B. Distance between A and B will be set to 0.5m, both located at the ground level. Participants will be asked to shovel construction materials with three different weights (i.e., dirt, cement, and gravel). Participants will be asked to shovel at a high-frequency rate (15 scoops per minute).
  • Task 2: Framing 30" wall using a power screwdriver. The frame will be placed on the floor, versus an elevated surface (28" height). Participants will be asked to use a power screwdriver to drive a screw into and out of the frame.
  • Task 3: Carrying construction materials of different weights (i.e., wood frames and pipes) for up to 10 meters in each trial. The maximum weight of the carried materials will not exceed 30 lbs.
  • Task 4: Lifting construction materials of different weights. The same materials will be used as the carrying task.
  • Task 5: Pounding a punching bag located in the ground vs. 18 inches high vs. 36 inches high using a sledgehammer of different weights (i.e., 0, 6, 12, 16, and 20 lbs.).
  • Task 6: Tying rebar in a framed grid located on different height levels (i.e., 0", 50").

The tasks and intensity levels were selected to be diverse yet reproducible (in terms of body postures) and resemble common tasks encountered in concrete work tasks.

Participants will be asked to answer questionnaires asking their experience, usability, and acceptability on each exoskeleton after they complete each work task.

The data collection process will end with removing optical markers and wearable sensors. Participants will be offered a rest break and refreshment if needed and followed by compensation and completing the payment form.

Conditions
Healthy
Being tested
Laevo 2, backX, FLx ErgoSkeleton, V22 ErgoSkeleton
Keywords
passive exoskeleton

What participants receive

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

  • Laevo 2Device

    The Laevo V2 is a wearable chest and back support exoskeleton. The Laevo transfers the from its chest pad to the thighs while bending forward. The passive exoskeleton (works with gas springs, not motors) transfers part of the load away from the back muscles, reducing the pressure on the spinal column. It provides a dampening effect on the back, reducing the risk of sudden back muscle contractions that needlessly overcompress the spine.

  • backXDevice

    backX is a novel industrial exoskeleton that substantially augments its wearer and reduces the forces and torques on a wearer's lower back region (L5/S1 disc) by an average of 60% while the wearer is stooping, lifting objects, bending or reaching. backX augments the wearer's strength and can reduce the risk of back injuries among workers. It does not require external motors or power source. The mechanism of backX is similar to the first device "Laevo 2".

  • FLx ErgoSkeletonDevice

    The FLx ErgoSkeleton is a range limiting work vest for physical work use. The FLx naturally reminds the user of the correct posture and lifting techniques while on the job site.

  • V22 ErgoSkeletonDevice

    Similar to the FLx ErgoSkeleton, the V22 ErgoSkeleton keeps the position of the human body as to always stay within a safe body posture while lifting or moving heavy objects. The V22 ErgoSkeleton applies pressure to remind the user both during improper lifts and over rotation.

    In addition, the V22 ErgoSkeleton comes with two clutch controlled cables to assist in lifting and moving. The cables transfer part of the weight of the object being held directly to the V22 ErgoSkeleton vest, similar to other arm and shoulder support exoskeletons.

Study groups in NCT04567797
Study groupRoleWhat they receive
ExoskeletonExperimentalTo compare the efficacy of four different exoskeleton devices, all participants will be asked to finish simulated construction tasks with each exoskeleton. Additionally, all participants will be asked to finish the same tasks without wearing an exoskeleton for reference.
Receives: Device: Laevo 2; Device: backX; Device: FLx ErgoSkeleton; Device: V22 ErgoSkeleton

What is being measured

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

  1. Muscle activities while performing simulated construction tasks

    Surface electromyography sensors will be placed on the following muscles of participants: Descending Trapezius (TRP), Anterior Deltoid (AD), Iliocostalis Lumborum (ILL), Rectus Abdominis (RA), External Oblique (EO), Cervical Erector Spinae (CES), Latissimus Dorsi (LD), and Vastus Lateralis (VL). Muscle activities while performing tasks represent the physical workload. Maximum Voluntary Contraction (MVC) technique will be used to normalize the muscle activities for comparison.

    Measured: From admission to discharge, up to 3 hours

  2. Body segment motions in a three-dimensional space measured by two methods

    Method 1: Wearable inertial sensors will be attached using hypoallergenic double-sided tape at the low-back near the waist (S1), upper back (T6), sternum, upper arm (R, L), lower arm (R, L), thigh (R, L), and shank (R, L). Body segment motions will be used to calculate relative angles, repetition count, duration of postures, which represent the physical workload of tasks.

    Method 2: Optical markers will be placed on anatomical landmarks of participants including the head, shoulders, arms, hands, back, pelvis, legs, and feet. The data collected my optical markers are mainly used for calibrating other sensors.

    Measured: From admission to discharge, up to 3 hours

Secondary outcomes (1)
  1. Subjective review of workload level and experience using different exoskeleton

    Participants will be asked a set of subjective review questions on a questionnaire with eight sections:

    The difficulty of tasks: From "Very Difficult" to "Very Easy". "Easier" means a better outcome.

    Effectiveness: From "Very unhelpful" to "Very helpful". More helpful means a better outcome.

    Pain/discomfort level: From "Just noticeable" to "Intolerable" for different body locations. Less pain or discomfort means a better outcome.

    Acceptability: From "Very Uncomfortable" to "Very Comfortable". More comfortable means a better outcome.

    Fit/wearability by himself: From "Very difficult" to "Very easy". Easier means a better outcome.

    Preference of using this exoskeleton again and recommending to other people: From "Very unlikely" to "Very likely". More likely means a better outcome.

    An overall experience by ranking all exoskeletons: Options include 4 exoskeletons and "No exoskeleton". A higher rank means a better outcome.

    Open-ended interview.

    Measured: From admission to discharge, up to 3 hours

Timeline

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

  1. First posted29 Sep 2020
  2. Study startOct 2020 (estimated)
  3. Primary completionDec 2020 (estimated)
  4. Study completionJan 2021 (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
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
25 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04567797
Sponsor's protocol ID
2007820207
Status last verified
Sep 2020
First submitted
4 Sep 2020
Last updated
29 Sep 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
No: IPD will not be shared to protect the privacy of participants.

Publications

  • Vera-Garcia FJ, Moreside JM, McGill SM. MVC techniques to normalize trunk muscle EMG in healthy women. J Electromyogr Kinesiol. 2010 Feb;20(1):10-6. doi: 10.1016/j.jelekin.2009.03.010.

    PubMed 19394867
  • Axler CT, McGill SM. Low back loads over a variety of abdominal exercises: searching for the safest abdominal challenge. Med Sci Sports Exerc. 1997 Jun;29(6):804-11. doi: 10.1097/00005768-199706000-00011.

    PubMed 9219209
  • Juker D, McGill S, Kropf P, Steffen T. Quantitative intramuscular myoelectric activity of lumbar portions of psoas and the abdominal wall during a wide variety of tasks. Med Sci Sports Exerc. 1998 Feb;30(2):301-10. doi: 10.1097/00005768-199802000-00020.

    PubMed 9502361
  • Kavcic N, Grenier S, McGill SM. Quantifying tissue loads and spine stability while performing commonly prescribed low back stabilization exercises. Spine (Phila Pa 1976). 2004 Oct 15;29(20):2319-29. doi: 10.1097/01.brs.0000142222.62203.67.

    PubMed 15480148
  • Allison GT, Godfrey P, Robinson G. EMG signal amplitude assessment during abdominal bracing and hollowing. J Electromyogr Kinesiol. 1998 Feb;8(1):51-7. doi: 10.1016/s1050-6411(97)00004-7.

    PubMed 9667034
  • O'Sullivan PB, Twomey L, Allison GT. Altered abdominal muscle recruitment in patients with chronic back pain following a specific exercise intervention. J Orthop Sports Phys Ther. 1998 Feb;27(2):114-24. doi: 10.2519/jospt.1998.27.2.114.

    PubMed 9475135
  • Vera-Garcia FJ, Elvira JL, Brown SH, McGill SM. Effects of abdominal stabilization maneuvers on the control of spine motion and stability against sudden trunk perturbations. J Electromyogr Kinesiol. 2007 Oct;17(5):556-67. doi: 10.1016/j.jelekin.2006.07.004. Epub 2006 Sep 22.

    PubMed 16996278
  • Vera-Garcia FJ, Brown SH, Gray JR, McGill SM. Effects of different levels of torso coactivation on trunk muscular and kinematic responses to posteriorly applied sudden loads. Clin Biomech (Bristol). 2006 Jun;21(5):443-55. doi: 10.1016/j.clinbiomech.2005.12.006. Epub 2006 Jan 27.

    PubMed 16442677
  • Rogers, E. (2020). The Survey of Occupational Injuries and Illnesses Respondent Follow-Up Survey. Monthly Labor Review.

  • Dong, X., Chowdhury, R., McCann, M., Trahan, C., & Gittle-man, J. S. (2008). The construction chart book: The US construction industry and its workers. In The Center for Construction Research and Training. Silver Spring.

  • West GH, Dawson J, Teitelbaum C, Novello R, Hunting K, Welch LS. An analysis of permanent work disability among construction sheet metal workers. Am J Ind Med. 2016 Mar;59(3):186-95. doi: 10.1002/ajim.22545. Epub 2016 Jan 21.

    PubMed 26792244
  • Marcum J, Adams D. Work-related musculoskeletal disorder surveillance using the Washington state workers' compensation system: Recent declines and patterns by industry, 1999-2013. Am J Ind Med. 2017 May;60(5):457-471. doi: 10.1002/ajim.22708. Epub 2017 Mar 15.

    PubMed 28295479
  • Ngo, B. P., Yazdani, A., Carlan, N., & Wells, R. (2017). Lifting height as the dominant risk factor for low-back pain and loading during manual materials handling: A scoping review. IISE Transactions on Occupational Ergonomics and Human Factors, 5(3-4), 158-171.

  • Kincl LD, Anton D, Hess JA, Weeks DL. Safety voice for ergonomics (SAVE) project: protocol for a workplace cluster-randomized controlled trial to reduce musculoskeletal disorders in masonry apprentices. BMC Public Health. 2016 Apr 27;16:362. doi: 10.1186/s12889-016-2989-x.

    PubMed 27121123
  • Dong, X., Betit, E., Dale, A., Barlet, G., and Wei, G. (2019). Trends of Musculoskeletal Disorders and Interventions in the Construction Industry. Quarterly Data Report by CPWR.

Questions about this trial

What is this clinical trial studying?

A study testing Laevo 2, backX and FLx ErgoSkeleton in people with Healthy, run by University of Arizona 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 2 inclusion and 7 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 29 Sep 2020. 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 Sol Lim, Ph.D. (520-626-0728, lims@arizona.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Muscle activities while performing simulated construction tasks (time frame: From admission to discharge, up to 3 hours). 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 NCT04567797, which also lists 21 linked publications.

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 29 Sep 2020.

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