Immediate Effect of Electrical Noise Stimulation on Neuromuscular Adaptation of Balance

October 6, 2022 updated by: National Yang Ming University

Immediate Effect of Electrical Noise Stimulation on Neuromuscular Adaptation During Single-Leg Stance in Healthy Young

Noise stimulation had an immediate effect on improving balance control. The present study aimed to clarify the immediate neuromuscular adaptation induced by noise stimulation and find the correlation between neuromuscular adaptation and functional performance.

Study Overview

Detailed Description

The mechanism behind noise stimulation is called Stochastic Resonance which improves the detectivity of sensory input with the presence of noise, making sub-sensory threshold input detectable. Noise stimulation had been proved to improve postural control, Ia afferent sensitivity, and muscle activity of the tibialis anterior. With this evidence of the effect of noise stimulation on balance enhancement, the neuromuscular adaptation induced by noise stimulation has not been researched yet. Therefore, the present study aims to clarify the immediate effect of noise on neuromuscular regulation during postural control.

Study Type

Interventional

Enrollment (Anticipated)

20

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Taipei, Taiwan, 112
        • National Yang-Ming University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years to 36 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • age between 20 and 40 years old
  • without ankle injury history in 1 year
  • without musculoskeletal or neurological diseases that would affect balance performance
  • without visual impairment (except vision correction or no visual problems)
  • without vestibular impairment.

Exclusion Criteria:

  • subject who cannot tolerate the cutaneous electrical stimulation to induce H reflex
  • single-leg stance (SLS) without support is shorter than 80 secs

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Sham stimulation on stable surface
The participant will not receive stimulation and will stand on flat ground.
Participants will not receive stimulation.
Experimental: Noise stimulation on stable surface
The participant will receive stimulation with intensity set at 90% of their sensory threshold and will stand on flat ground.
The intensity of electrical noise stimulation will be set at 90% of the sensory threshold of each participant.
Experimental: Sham stimulation on unstable surface
The participant will not receive stimulation and will stand on foam.
Participants will not receive stimulation.
The foam will be used to make an unstable surface.
Experimental: Noise stimulation on unstable surface
The participant will receive stimulation with intensity set at 90% of their sensory threshold and will stand on foam.
The intensity of electrical noise stimulation will be set at 90% of the sensory threshold of each participant.
The foam will be used to make an unstable surface.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mean sway path of the center of pressure
Time Frame: 40 seconds under each condition
The mean sway path in mm will represent balance performance
40 seconds under each condition
Mean sway velocity of the center of pressure
Time Frame: 40 seconds under each condition
The mean sway velocity in mm/sec will represent balance performance
40 seconds under each condition
Cortical excitability
Time Frame: 40 seconds under each condition
Power spectrum density of EEG will calculated for representing cortical excitability.
40 seconds under each condition
Spinal reflex excitability
Time Frame: 40 seconds under each condition
H reflex amplitude will represent the excitability of peripheral control from spinal level nerve system.
40 seconds under each condition
Co-activation index
Time Frame: 40 seconds after each condition
Co-activation index will be calculated by EMG activity of Tibialis Anterior and Soleus muscle to represent the muscle activity.
40 seconds after each condition

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Li-Wei Chou, PhD, National Yang Ming Chiao Tung University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 29, 2022

Primary Completion (Anticipated)

November 30, 2022

Study Completion (Anticipated)

January 31, 2023

Study Registration Dates

First Submitted

August 14, 2022

First Submitted That Met QC Criteria

October 6, 2022

First Posted (Actual)

October 7, 2022

Study Record Updates

Last Update Posted (Actual)

October 7, 2022

Last Update Submitted That Met QC Criteria

October 6, 2022

Last Verified

July 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

IPD Plan Description

The informed Consent Form used in this research does not mention IPD sharing.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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