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HealthyNCT07050784

Wearable Garment vs Gel Electrodes for Electrical Muscle Stimulation

A study testing Hydrogel electrodes, Dry polymer-textile electrodes with Skin Lotion A and Dry textile electrodes with gel pads attached to the electrode in people with Healthy, run by Myant Medical Corp. at 1 site in Canada.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The goal of this study is to evaluate whether textile-based electrodes can provide neurostimulation that is comparable in comfort and effectiveness to traditional hydrogel electrodes in healthy adults. The main questions it aims to answer are: 1. 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?
Hydrogel electrodes, Dry polymer-textile electrodes with Skin Lotion A and Dry textile electrodes with gel pads attached to the electrode
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
1 siteCanada
Study dates
1 Jul 2025to Sep 2025
Phase
Interventional
Are there results?
Not yet: the study is under way

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

  • Healthy (without a known diagnosis of cardiovascular, pulmonary or neurological condition)

Who cannot join

  • Known pregnancy
  • Implanted defibrillator or pacemaker
  • Pain in the body part being tested
  • Open wound or dressing (e.g. band-aid) on a body part that needs to be in contact with the electrodes
  • Severe frailty such that donning or doffing the garment may cause a danger of falling

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Amirali Toossi contact

4164237906

amirali.toossi@myant.ca

Canada1 site
  • Myant Medical Corp

    Mississauga, Ontario, L5K 2L1

    Amirali Toossi, 4164237906, amirali.toossi@myant.ca

Other trials in Canada

About this study

Official title: A Crossover Randomized Controlled Trial Comparing Smart Textile and Hydrogel Electrodes for Neurostimulation in Healthy Adults

The goal of this study is to evaluate whether textile-based electrodes can provide neurostimulation that is comparable in comfort and effectiveness to traditional hydrogel electrodes in healthy adults.

The main questions it aims to answer are:

Read more
  1. Is the perceived sensation of stimulation using textile electrodes non-inferior to that of hydrogel electrodes?
  2. Is the current required to evoke muscle contractions similar between textile and hydrogel electrodes?

Each participant will complete three stimulation conditions in random order across separate visits:

  1. hydrogel electrodes (standard),
  2. dry polymer-textile electrodes with lotion, and
  3. dry textile electrodes with hydrogel pads

Electrical stimulation will be delivered to the lower leg muscles using a wearable sleeve with integrated electrodes. The investigators will assess sensorimotor thresholds (e.g., detection, motor, and full motor threshold), skin-electrode impedance, and torque. Participants will also rate stimulation comfort, intensity, and sensation location via questionnaire.

After the three primary arms, participants may optionally complete two additional arms using different moisturizers applied to the textile electrodes to evaluate their impact on stimulation performance.

The results of this study will help determine whether textile electrodes can be used as an effective and comfortable alternative to hydrogel electrodes in wearable neurostimulation applications.

Read the detailed description

Neurostimulation involves the use of electric current delivered through skin-surface electrodes to activate muscles. It is commonly used for purposes such as muscle strengthening, motor function improvement, blood flow enhancement, and in neuroprostheses. Standard neurostimulation systems typically rely on disposable hydrogel electrodes, which can cause skin irritation and tend to dry out over time. These limitations make hydrogel electrodes less suitable for long-term or repeated use.

Textile-based electrodes are an emerging alternative. These electrodes are integrated into wearable garments, making them washable, reusable, and more comfortable for extended wear times. However, research directly comparing their effectiveness and user experience compared to hydrogel electrodes is limited.

The goal of this study is to compare textile electrodes to gold-standard hydrogel electrodes for muscle activation and perceived stimulation sensation. The investigators hypothesize that: 1) there will be no clinically meaningful difference in participants' perception of the stimulation between textile and hydrogel electrodes, and 2) there will be no significant difference in the stimulation current required to elicit functional contractions.

This is a crossover randomized controlled trial involving three primary arms: 1) hydrogel electrodes, 2) dry polymer-textile electrodes with lotion, and 3) dry textile electrodes with gel pads applied. Each participant will perform all three arms in a randomized order with at least 24 hours between visits. Stimulation will be delivered to the calf and tibialis anterior muscles using the same electrical stimulator and settings in all conditions. Following completion of the three primary arms, participants will be given the option to complete an additional two arms using different types of commercially available moisturizers on the dry textile electrodes to assess comparative on-body performance of different water-based moisturizers. All moisturizers are commercially available and are labelled Skin Lotion A, B, and C in the 'Arms and Interventions' section.

A sample size of 18 participants is required to detect a Cohen's f of 0.40 with 95% power and a significance level of ⍺ = 0.05 for a within-subjects one-way repeated measures analysis of variance (ANOVA) with three conditions. To preserve statistical power, the investigators will recruit 20 participants. Pilot data comparing textile to hydrogel electrodes provided an estimated effect size of f = 0.65. Given the pilot data was not randomized, which likely inflated the observed effect size, the investigators conservatively based their sample size calculation on a Cohen's f of 0.40 (i.e., a large effect size) to ensure adequate power to detect a potentially smaller true effect.

A non-inferiority analysis will compare perceived stimulation intensity on a 10-point numerical rating scale. A 2-point difference is set as the non-inferiority margin based on prior research on the minimal clinically important difference. Textile electrodes will be considered non-inferior if the upper bound of the 95% confidence interval for the difference in intensity remains below this threshold. Repeated measures ANOVAs and Tukey's post hoc tests will be used to analyze the outcome variables where appropriate.

Conditions
Healthy
Being tested
Hydrogel electrodes, Dry polymer-textile electrodes with Skin Lotion A, Dry textile electrodes with gel pads attached to the electrode, Dry polymer-textile electrodes with Skin Lotion B, Dry polymer-textile electrodes with Skin Lotion C
Keywords
Textile electrodes, Smart clothing, Neuromuscular electrical stimulation, Transcutaneous electrical nerve stimulation, Functional electrical stimulation

What participants receive

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

  • Hydrogel electrodesDevice

    Neurostimulation using standard self-adhesive hydrogel electrodes

  • Dry polymer-textile electrodes with Skin Lotion ADevice

    Neurostimulation with dry polymer-textile electrodes using Skin Lotion A

  • Dry textile electrodes with gel pads attached to the electrodeDevice

    Neurostimulation with dry textile electrodes with gel pads attached to the electrode

  • Dry polymer-textile electrodes with Skin Lotion BDevice

    Neurostimulation with dry polymer-textile electrodes with Skin Lotion B

  • Dry polymer-textile electrodes with Skin Lotion CDevice

    Neurostimulation with dry polymer-textile electrodes using Skin Lotion C

Study groups in NCT07050784
Study groupRoleWhat they receive
Hydrogel electrodesActive comparatorGold-standard comparator
Receives: Device: Hydrogel electrodes
Dry polymer-textile electrodes with Skin Lotion AExperimentalNot described
Receives: Device: Dry polymer-textile electrodes with Skin Lotion A
Dry textile electrodes with gel pads attached to the electrodeExperimentalNot described
Receives: Device: Dry textile electrodes with gel pads attached to the electrode
Dry polymer-textile electrodes with Skin Lotion BExperimentalNot described
Receives: Device: Dry polymer-textile electrodes with Skin Lotion B
Dry polymer-textile electrodes with Skin Lotion CExperimentalNot described
Receives: Device: Dry polymer-textile electrodes with Skin Lotion C

What is being measured

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

  1. Perceived intensity of stimulation

    Participants will rate the perceived intensity of electrical stimulation at the current required to elicit 20% of their maximal voluntary contraction (MVC). Intensity will be assessed using a 10-point numerical scale, where 0 represents no sensation and 10 represents painful stimulation.

    Measured: At each of the 5 study visits (Visit 1 through Visit 5) over approximately a 3-week period.

Secondary outcomes (5)
  1. Sensorimotor responses to electrical stimulation

    Current amplitude required to elicit various sensorimotor responses will be recorded.

    Participants will receive electrical stimulation to the lower leg. The study will measure:

    • Detection threshold: the smallest current the participant can feel.
    • Motion threshold: the lowest current that causes visible movement.
    • Full range of motion amplitude: the current needed for full joint range of motion.
    • Just noticeable difference: the smallest change in current a participant can detect.

    Stimulation will be increased gradually and stopped if discomfort is reported. All stimulation will not exceed safe current limits (i.e., 100 mA).

    Measured: At each of the 5 study visits (Visit 1 through Visit 5) over approximately a 3-week period.

  2. Kinematic recruitment curves

    Kinematic recruitment curves will be created by measuring ankle movement during stimulation. A camera will record the ankle as stimulation amplitude increases in small increments. Joint angles will be measured from the video and plotted against stimulation intensity to produce kinematic recruitment curves.

    Measured: At each of the 5 study visits (Visit 1 through Visit 5) over approximately a 3-week period.

  3. Torque

    Maximum voluntary contraction (MVC) will be determined through three maximal effort contractions of the ankle. Electrical stimulation will then be applied to determine the current required to produce 20% of the MVC.

    Measured: At each of the 5 study visits (Visit 1 through Visit 5) over approximately a 3-week period.

  4. Sensation questionnaire

    Participants will complete a questionnaire following stimulation to report:

    • How the stimulation felt
    • Where it was felt
    • How comfortable it was, rated on a 7-point scale, with 0 being comfortable and 7 being uncomfortable

    Measured: At each of the 5 study visits (Visit 1 through Visit 5) over approximately a 3-week period.

  5. Skin-electrode impedance

    To measure electrical impedance, a small electrical signal will be sent through the electrodes across a range of frequencies, and resistance will be recorded. This helps evaluate how well the electrodes conduct current during use.

    Measured: At each of the 5 study visits (Visit 1 through Visit 5) over approximately a 3-week period.

Timeline

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

  1. First posted3 Jul 2025
  2. Study start1 Jul 2025 (estimated)
  3. Primary completionSep 2025 (estimated)
  4. Study completionSep 2025 (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
Basic science
Allocation
Randomised
Intervention model
Crossover
Model description
Crossover randomized controlled trial
Masking
None (open label)
Enrolment
20 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07050784
Sponsor's protocol ID
157491
Status last verified
Jun 2025
First submitted
9 Jun 2025
Last updated
8 Jul 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Study is internal

Questions about this trial

What is this clinical trial studying?

A study testing Hydrogel electrodes, Dry polymer-textile electrodes with Skin Lotion A and Dry textile electrodes with gel pads attached to the electrode in people with Healthy, run by Myant Medical Corp. at 1 site in Canada.

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 1 inclusion and 5 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: opening soon, as of the sponsor's last update on 8 Jul 2025. 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 Canada. 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?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Amirali Toossi (4164237906, amirali.toossi@myant.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Perceived intensity of stimulation (time frame: At each of the 5 study visits (Visit 1 through Visit 5) over approximately a 3-week period.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 8 Jul 2025.

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