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NCT Number: NCT07273422

Novel Self-charging, Medical-Grade Smart Insoles With AI/ML Edge Computing to Monitor Biometrics.

This study will evaluate the effectiveness of newly developed self-powered, smart insoles that will be used for remote patient monitoring (RPM) for both military and civilian populations. The present study is part of a project funded by SEMI and the Air Force Research Laboratory (AFRL).

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Key information

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Spectrum Ergonomics and Occupational Health Services

Williamsport, Pennsylvania, 17701, United States

Location status: Recruiting

Location contact

Helen Hiserman, MS

SUB_INVESTIGATOR

Jeff Hiserman, Bachelor's

CONTACT

[email protected]

5704953298

Jeff Hiserman, Bachelor's

PRINCIPAL_INVESTIGATOR

Robert Andosca, PhD

CONTACT

[email protected]

(617) 447-1876

About this study

The present study, funded jointly by SEMI and the AFRL, is intended to evaluate the comfort, durability, and sensor accuracy of the smart insoles and associated mobile app. The study will evaluate both generation 1.0 and generation 2.0 of the smart insole. The primary difference between the two generations is the that gen 2.0 will use an improved energy harvester for power generation.

The present study is structured in two phases. Phase 1 will evaluate gen 1.0 of the insole in a pilot study at the University of Utah (U of U) with 10 subjects. The subjects will be asked to wear the insole while walking at different speeds on an instrumented treadmill in the Motion Core Analysis Facility at the University of Utah and asked to walk over a ½ mile course on the U of U campus. This study will be overseen by Dr. Shad Roundy.

Phase 2 will evaluate gen 2.0 of the insole. A pilot study will take place at the U of U and will mimic the phase 1 study with 10 subjects. Again, the study will be overseen by Dr. Shad Roundy. This will be followed up by a larger field study with 100 subjects who will be asked to take the insoles home and wear them over the course of 4 weeks. The field study will be overseen by Dr. Jeff Hiserman at Spectrum Ergonomics.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participant is generally health and between 18 and 90 year of age at time of signing consent.
  • Participant must be available for 4 visits to Spectrum Ergonomics over a 4-week period, one visit per week.

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Exclusion criteria

  • Age of Participants: 18-90

Sample Size:

At Utah:

All Centers: 120

Inclusion criteria

Inclusion criteria

for Phase 1 and Phase 2 pilot studies at UofU

  • Participant is generally healthy and between 18 and 90 years of age at time of signing consent 2. Participant must be able to walk comfortably for 1 mile. 3. Will seek 5 male and 5 female participants. Inclusion criteria for Phase 2 field studies conducted by Spectrum Ergonomics
  • Participant is generally health and between 18 and 90 year of age at time of signing consent.
  • Participant must be available for 4 visits to Spectrum Ergonomics over a 4-week period, one visit per week.

Exclusion criteria

Exclusion criteria

for Phase 1 and Phase 2 pilot studies at UofU

  • Flat feet (Pes planus)
  • Unilateral leg amputee
  • Females who are pregnant, < 3 months postpartum, or currently lactating.
  • Major surgery < 6 months or minor surgery < 3 months before enrollment.
  • Major infections such as sepsis or pneumonia < 3 months before enrollment.
  • Myocardial infarction or heart failure < 5 years or less before enrollment.
  • Ankle fusion or total replacement
  • Morbid obesity BMI > 40.

Exclusion criteria

for Phase 2 field study at Spectrum Ergonomics

  • Flat feet (Pes planus) or high arches (Pes cavus)
  • Unilateral leg amputee.
  • Brittle Diabetes- hard-to-control diabetes (also called labile diabetes), which is characterized by wide variations in blood glucose in which blood glucose levels can quickly move from too high (hyperglycemia) to too low (hypoglycemia).
  • Peripheral neuropathy.
  • Loss of sensation in the sole of foot.
  • Open wound on the foot.
  • Females who are pregnant, < 3 months postpartum, or currently lactating.
  • Ankle fusion or total replacement
  • Major surgery < 6 months or minor surgery < 3 months before enrollment.
  • Major infections such as sepsis or pneumonia < 3 months before enrollment.
  • Myocardial infarction or heart failure < 1 years before enrollment.
  • Morbid obesity BMI > 40.

Treatment and study plan

Observational with data collected

Other

Observational with data collection from sensors in insole

Primary outcomes

  1. The present study is intended to evaluate the safety of the sensors embedded in the smart insoles and their accuracy in measuring biomarkers.

    Time frame: "From enrollment to the end of observations at 4 weeks"

    The sensors will measure: Pulse Oxygen as the percentage saturation of oxygen carried in the red blood cells.

Secondary outcomes

  1. The present study is intended to evaluate the safety of the sensors embedded in the smart insoles and their accuracy in measuring biomarkers.

    Time frame: Time Frame: "From enrollment to the end of observations at 4 weeks"

    Description: The sensors will measure: Heart Rate and Heart Rate Variability in beats per minute.

Other outcomes

  1. The present study is intended to evaluate the safety of the sensors embedded in the smart insoles and their accuracy in measuring biomarkers.

    Time frame: Time Frame: "From enrollment to the end of observations at 4 weeks"

    Description: The sensors will measure: Body temperature as measured in degrees Celsius.

Study contacts

Contact information is provided by the study sponsor or research team.

Jeff Hiserman, Bachelor's

CONTACT

[email protected]

15704953298

Ryane Sorenson, Bachelor's

CONTACT

[email protected]

801-585-0302

Sponsors and collaborators

Lead sponsor

Spectrum Ergonomics and Occupational Health Services

Industry

Collaborators

  • United States Air Force Research Laboratory
  • University of Utah

Registry information

Official study title

Evaluation of Self-powered Smart Insoles

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Dec 9, 2025
Registry last updated
Dec 9, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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