Evaluation of a Soft Exoskeleton to Support Forward Leaning and Lifting

Sponsor
Swiss Federal Institute of Technology (Other)
Overall Status
Recruiting
CT.gov ID
NCT05097612
Collaborator
Auxivo AG (Other)
30
1
1
7.7
3.9

Study Details

Study Description

Brief Summary

In this study the LiftSuit version 2.0 designed by Auxivo AG will be used. The LiftSuit is a soft wearable device that is designed to support workers perform physically demanding tasks including repetitive lifting and working in forward leaning positions. It is put on like a backpack and attached to the body using fabric bands and cuffs. Besides soft fabric parts the LiftSuit contains elastics elements. The elastic elements can be flexibly exchanged by the experimenter. For this experiment elastic elements of known stiffness will be hooked into the fabric frame.

Condition or Disease Intervention/Treatment Phase
  • Device: Placebo LiftSuit Exoskeleton
  • Device: LiftSuit Exoskeleton (low support level)
  • Device: LiftSuit Exoskeleton (medium support level)
  • Device: LiftSuit Exoskeleton (high support level)
N/A

Detailed Description

In a first step participants will try on the LiftSuit exoskeleton and adjust it to their body under supervision of the experimenter. When the LiftSuit exoskeleton is adjusted to the participant it is taken off to allow placement of sensors. The sensors used to record heart rate (Polar H9 heart rate monitor, Polar Electro Europe AG, Germany), muscle activity from 8 muscles in the back and hip region (Delsys Trigno, Delsys Europe, United Kingdom) and movement kinematics (OptiTrack motion capture system, NaturalPoint Inc., USA) will be placed by the experimenter (or participant him/herself). To verify that the electromyography sensors, are working and to obtain normalization values, participants will be instructed to conduct maximal voluntary contractions of each muscle that are being recorded. If needed single sensors can be replaced. After this the exoskeleton will be put back on.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
"Evaluation of a Soft Exoskeleton With Parallel Springs and Its Ability to Reduce Physical Load During Lifting and Leaning"
Actual Study Start Date :
Nov 8, 2021
Anticipated Primary Completion Date :
Jul 1, 2022
Anticipated Study Completion Date :
Jul 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Healthy participant

This is a repeated measures design. All participants receive both the intervention and the placebo comparator.

Device: Placebo LiftSuit Exoskeleton
The LiftSuit is a soft passive wearable device that is designed to support the hip and back muscles during forward leaning and lifting. It exerts it function through Elastic Energy Storages (EES). In this condition the EES are removed from the device to create a placebo device.

Device: LiftSuit Exoskeleton (low support level)
The LiftSuit is a soft passive wearable device that is designed to support the hip and back muscles during forward leaning and lifting. It exerts it function through Elastic Energy Storages (EES). EES of different three different levels of stiffness (low, medium, high stiffness) will be used.

Device: LiftSuit Exoskeleton (medium support level)
The LiftSuit is a soft passive wearable device that is designed to support the hip and back muscles during forward leaning and lifting. It exerts it function through Elastic Energy Storages (EES). EES of different three different levels of stiffness (low, medium, high stiffness) will be used.

Device: LiftSuit Exoskeleton (high support level)
The LiftSuit is a soft passive wearable device that is designed to support the hip and back muscles during forward leaning and lifting. It exerts it function through Elastic Energy Storages (EES). EES of different three different levels of stiffness (low, medium, high stiffness) will be used.

Outcome Measures

Primary Outcome Measures

  1. Change in muscle activity of hip extensor muscles (placebo comparator - low support experimental intervention) [2 hours]

    An elastic band placed external to the body parallel to the spine and over the hip joint is likely to support the muscles that extend the hip and back. Less hip extensor muscle (m. gluteus maximus, hamstrings) activity is expected in LiftSuit conditions compared to the placebo comparator condition.

  2. Change in muscle activity of back extensor muscles (placebo comparator - low support experimental intervention) [2 hours]

    An elastic band placed external to the body paralell to the spine and over the hip joint is likely to support the muscles that extend the hip and back. Less back muscle activity (erector spinae at lumbar and thoracic level) is expected in LiftSuit conditions compared to the placebo comparator condition.

Secondary Outcome Measures

  1. Change in muscle activity of hip extensor muscles related to stiffness level of the Elastic Energy Storages (low, medium, high stiffness). [2 hours]

    A reduction in muscle activity is expected. This reduction is expected to be related to the stiffness level of the EES. With high stiffness, leading to more support, leading to less muscle activity.

  2. Change in muscle activity of back muscles related to stiffness level of the Elastic Energy Storages (low, medium, high stiffness). [2 hours]

    The reduction in muscle activity is expected to be related to the stiffness level of the EES. With high stiffness, leading to more support, leading to less muscle activity.

Other Outcome Measures

  1. Change in muscle activity of abdominal muscles (placebo comparator - experimental intervention) [2 hours]

    An elastic band placed external to the body over the hip joint is likely to support the muscles that extend the hip. It could be that this setup might heightened levels of activity in the abdomen.

  2. Change in hip angle kinematics (placebo comparator - experimental intervention) [2 hours]

    Changed forces around the hip joint might influence movement kinematics of this joint. Changes in position and acceleration of the joint angle will be calculated.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Included will be volunteers of both sexes within working age (18 to 65 years).
Exclusion Criteria:
  • Participants will be excluded if they cannot perform the tasks (squat lifting and forward leaning) due to physical limitations. Furthermore, people who report acute joint or muscle pain or stiffness, or a self-reported history of such problems will be excluded.

Contacts and Locations

Locations

Site City State Country Postal Code
1 ETH Zurich, Rehabilitation Engeineering Laboratory Zurich Switzerland 8008

Sponsors and Collaborators

  • Swiss Federal Institute of Technology
  • Auxivo AG

Investigators

  • Principal Investigator: Olivier Lambercy, PhD, Swiss Federal Institute of Technology

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Swiss Federal Institute of Technology
ClinicalTrials.gov Identifier:
NCT05097612
Other Study ID Numbers:
  • ETH EK 2021-N-151
First Posted:
Oct 28, 2021
Last Update Posted:
Apr 14, 2022
Last Verified:
Jan 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Apr 14, 2022