Validation of Smart Garments for Metabolic Rate Estimation

Sponsor
Myant Inc. (Industry)
Overall Status
Recruiting
CT.gov ID
NCT06026761
Collaborator
University of Waterloo (Other)
20
1
9.2
2.2

Study Details

Study Description

Brief Summary

The goal of this observational study is to assess the use of Myant Skiin garments for the purpose of estimating metabolic rate in 20 adult (18-64 yrs) healthy participants. The main question it aims to answer is What is the accuracy of metabolic rate estimate from the Skiin algorithm utilizing Skiin data, as compared to observation and a gold-standard sensor?

Participants will be asked to perform a number of scripted tasks and their data will be assessed and compared against gold standard wearable indirect calorimetry device (COSMED K5) measurements.

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Condition or Disease Intervention/Treatment Phase
  • Device: Skiin garment and pods

Detailed Description

  1. Following consent, the participants will first be asked to fill out a participant information questionnaire.

  2. Equipment setup - SKIIN: For the SKIIN garments, participants will use the elastic research belt for the study. The belt is an fabric, elastic strap that has been washed and sanitized to be worn over the skin at the chest or waist. A private area for changing will be provided. The SKIIN sensor pod will be attached to the holster on the belt to collect inertial measurement unit (IMU) data and electrocardiography (ECG) data similar to the motion and cardiac sensors in many wrist-worn activity tracking systems (e.g., Apple Watch). The electrodes must be in contact with the skin to acquire ECG data. Data from the Skiin garments will be acquired using the custom research interface provided by the supplier. The data is acquired wirelessly and stored on the local computer (and no data is sent to the cloud).

  3. Equipment setup - K5 COSMED: For the reference/criterion- standard metabolic measurement system, a wearable indirect calorimetry system will be used. This system comprises of a mask fitted over the mouth and nose connected to a portable device that analyzes breath gas composition and volume. The mask has been cleaned and sanitized prior to use with a participant. The data is acquired on the device and stored on a local computer (no data is sent to the cloud).

  4. Once the equipment has been set up for the participant, an overview of the activities and exercise tasks to be conducted during the protocol will be demonstrated.

  5. Exercise tasks are described in more detail in the attached document. In general, all exercises can be modified by the participant to modulate intensity

Study Design

Study Type:
Observational
Anticipated Enrollment :
20 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Validation of Myant Skiin Smart Garments for Metabolic Rate Estimation
Actual Study Start Date :
Mar 28, 2023
Anticipated Primary Completion Date :
Jan 1, 2024
Anticipated Study Completion Date :
Jan 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Healthy individuals

Metabolic study protocol

Device: Skiin garment and pods
Participants will be asked to wear two pieces of equipment to record physiological data: A Skiin garment that contains IMU and ECG sensors A Cosmed K5 metabolic cart that will record breathing rate data Participants will then be asked to perform various tasks of daily living (e.g. watching TV, sweeping the floor), general strength exercises (e.g. squats, triceps dips, lunges), and aerobic exercises (e.g. walking, running) as instructed by researchers

Outcome Measures

Primary Outcome Measures

  1. Heart rate [Through study completion (1 hour total), average heart rate calculated every 1 minute]

    Heart rate obtained via ECG from the Skiin device

  2. Metabolic rate [Through study completion (1 hour total), average metabolic rate calculated every 1 minute]

    Metabolic rate obtained via the gold standard portable metabolic cart (COSMED K5)

  3. Acceleration /Activity counts [Through study completion (1 hour total), average activity calculated every 1 minute]

    Epoch-based physical activity counts using accelerometer data obtained through Skiin device

Secondary Outcome Measures

  1. Age [During participant inclusion]

    Participant age

  2. Sex [During participant inclusion]

    Participant sex (male, female, other)

  3. Weight [During participant inclusion]

    Participant weight (kg)

  4. Height [During participant inclusion]

    Participant height (cm)

  5. Fitness Level [During participant inclusion]

    Participant self-reported fitness level (sedentary, low, moderate, high, very high)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 64 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Healthy male and female adult volunteers (18y - 64y old)

must answer No to the following:

  • Have you had musculoskeletal and/or neurological foot, ankle, knee, or hip conditions, such as stroke, arthritis, trauma, joint surgery?

  • Have you been diagnosed with a neurological disorder or cognitive impairment such as Alzheimer's disease, migraine, epilepsy, dementia, Parkinson's disease, brain tumors, multiple sclerosis?

  • Have you experienced a diagnosed concussion or brain trauma in the past 6 months?

  • Do you have a condition that limits your capacity for aerobic exercise (e.g., asthma, cardiac condition)?

Exclusion Criteria:
  • individuals with (self-reported) lower limb conditions, neurological disorders, history of concussion/brain trauma, and/or condition limiting exercise is to mitigate additional risk for injury and/or adverse reactions associated with exercise activities.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Waterloo - Engineering 7 Waterloo Ontario Canada N2L 3G1

Sponsors and Collaborators

  • Myant Inc.
  • University of Waterloo

Investigators

  • Principal Investigator: James Tung, PhD, Waterloo University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Myant Inc.
ClinicalTrials.gov Identifier:
NCT06026761
Other Study ID Numbers:
  • Myant/Waterloo/44441
First Posted:
Sep 7, 2023
Last Update Posted:
Sep 7, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Myant Inc.

Study Results

No Results Posted as of Sep 7, 2023