Assessment of Upper Limb Motor Performance Using an Interface With Haptic Feedback

Sponsor
Universidad Nacional de Entre Rios (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05819047
Collaborator
(none)
30
1
2
15

Study Details

Study Description

Brief Summary

The purpose of the study is to test an evaluation environment based on a device that has the ability to provide the user with tactile (haptic) sensations. This environment will be used to investigate how the arm movements of a healthy person are performed, and then - at a later stage - to find out whether it is possible to measure changes during musculoskeletal pain. Electrical signals produced by the brain (called electroencephalogram or EEG) will be recorded by means of electrodes on the surface of the scalp (non-invasive). In addition, the angle of the elbow joint during movement will be measured, with the intention of using objective measures to aid future evidence-based clinical decision making.

It is expected that the developed environment can be used -in the near future-, to evaluate the progression of pathologies associated with muscle pain, or to quantify the effectiveness of rehabilitation therapies.

Condition or Disease Intervention/Treatment Phase
  • Device: Functional test with a haptic device

Detailed Description

Experimental setup Volunteers will be received at the Center of Rehabilitation Engineering and Neuromuscular and Sensory Research (CIRINS). They will be informed, in simple terms, of the purpose of the project and the measurements that will be done during the session. The Informed Consent Form will be read to each volunteer and, if they decide to participate, they will be asked to sign a copy that will be filed in the Laboratory together with their contact information, which will be stored confidentially.

At the beginning of the session, the volunteer will be asked to sit comfortably. The EEG electrodes will then be attached using a 16-electrode cap in the standard 10-20 location, together with the exoskeleton in the position determined by the investigator. The position of the camera that will be used to follow the movements of the upper limb will also be adjusted to ensure that the movements will be within the camera's field of view.

Subsequently, the subject will be placed in its initial position: seated, with approximately 45° of shoulder abduction, 10° of shoulder flexion and 90° of elbow flexion.

Once the subject is in the proper position, they will be asked, using the implemented test interface, to perform the virtual nine-hole peg test (NHPT) in Cue Based and Self Paced variants. The volunteer will be asked to complete these tests with both hands, in order to assess whether there are differences in performance associated with the side with which the test is performed, and whether using the system is sensitive enough to detect these changes. The researcher conducting the experiment should record which test was performed with the dominant hand and which was not.

To evaluate whether the results obtained are satisfactory, they will be compared with those reported for healthy individuals.

Evaluation tests Cue-based nine-hole peg test: this test works with time or event dependent cues, dividing the test into several repetitions of the same task. Each trial starts at the same predetermined position, and consists of placing as quickly as possible a random peg in a random hole. This randomness is given in the order of the first nine attempts without repeating the peg. Then, in case of additional attempts, the order of the first nine attempts is repeated. In case of failure to complete an attempt within a certain time or placing the peg in the wrong hole, it is given as failed. The signals presented to the user are visual. The pegs change color from white (inactive) to red, which marks the peg that should move (but without giving the signal to move yet), when the peg changes to green, the movement should begin. Likewise, the hole into which the peg should be inserted is marked with the addition of a translucent light blue object. Inactive holes have no color or object inside. At the end of a repetition, the position of the pegs is reset. The starting point of each repetition of the test is marked with a translucent sphere, which is the position that the robot cursor must take before the next attempt. This object sees its position reflected along with the other elements of the virtual environment when changing hands.

Self-paced nine-hole peg test : this test gives the user the freedom to place the desired peg in the desired hole at the desired speed. This test is the most similar to the original NHPT, and ends when all nine pegs are placed in the nine holes, giving as a result the total duration of the test.

Study Design

Study Type:
Observational
Anticipated Enrollment :
30 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
Assessment of Upper Limb Motor Performance Using an Interface With Haptic Feedback
Anticipated Study Start Date :
Apr 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2023
Anticipated Study Completion Date :
Jun 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Healthy

Healthy volunteers

Device: Functional test with a haptic device
Volunteers will complete two tests based on the Nine Hole Peg Test with a haptic device.

Outcome Measures

Primary Outcome Measures

  1. Movement smoothness [Average of 36 trials during a single experimental session with a duration of 30 minutes]

    Smoothness of the participant movement calculated through the fourth derivative of the trajectory (jerk).

Secondary Outcome Measures

  1. Log jerk transport [Average of 36 trials during a single experimental session with a duration of 30 minutes]

    Smoothness of the peg transport trajectory, from the initial position to the hole.

  2. Log jerk return [Average of 36 trials during a single experimental session with a duration of 30 minutes]

    Smoothness of the return trajectory, from the position of the hole where the last peg was inserted to the initial position of the next peg.

  3. SPARC return [Average of 36 trials during a single experimental session with a duration of 30 minutes]

    Smoothness of the return trajectory, from the position of the hole where the last peg was inserted to the initial position of the next peg.

  4. Path length ratio transport [Average of 36 trials during a single experimental session with a duration of 30 minutes]

    Efficiency of the peg transport trajectory, from the initial position to the hole.

  5. Path length ratio return [Average of 36 trials during a single experimental session with a duration of 30 minutes]

    Efficiency of the return trajectory, from the position of the hole where the last peg was inserted to the initial position of the next peg.

  6. Velocity max. return [Average of 36 trials during a single experimental session with a duration of 30 minutes]

    Maximum velocity during the return trajectory, from the position of the hole where the last peg was inserted to the initial position of the next peg.

  7. Jerk peg approach [Average of 36 trials during a single experimental session with a duration of 30 minutes]

    Precision of the ballistic movement during the approach to the peg (near the end of the return and just before the beginning of transport).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • No history of neurological disease, chronic pain, or musculoskeletal disorders.

  • Willingness and ability to fully understand the content and scope of the experiment and to comply with the instructions.

  • Signature of the informed consent document.

Exclusion Criteria:
  • Pregnancy.

  • History of chronic pain or neuromuscular disorders.

  • History of addictive behavior, defined as abuse of alcohol, cannabis, opioids or other drugs.

  • History of heat sensitivity disorders.

  • Presence of fever, tuberculosis, malignant tumors, infectious processes, acute inflammatory processes.

  • Implantation of pacemakers or metallic prostheses.

  • Use of analgesics within 24 hours prior to participation in the experiment.

  • Lack of cooperation.

  • Trauma of the segment to be evaluated in the last 4 weeks.

  • Surgical history of the upper quadrant.

  • Metabolic diseases.

  • Ingestion of pain medication in the last 24 hs.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Facultad de Ingeniería, Universidad Nacional de Entre Ríos Oro Verde Entre Ríos Argentina 3100

Sponsors and Collaborators

  • Universidad Nacional de Entre Rios

Investigators

  • Principal Investigator: Rosa M Weisz, MSc. in Biomed Eng, Universidad Nacional de Entre Rios

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Rosa María Weisz, Principal Investigator, Universidad Nacional de Entre Rios
ClinicalTrials.gov Identifier:
NCT05819047
Other Study ID Numbers:
  • IS003960
First Posted:
Apr 19, 2023
Last Update Posted:
Apr 21, 2023
Last Verified:
Apr 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Rosa María Weisz, Principal Investigator, Universidad Nacional de Entre Rios

Study Results

No Results Posted as of Apr 21, 2023