Wearable Wireless Respiratory Monitoring System That Detects and Predicts Opioid Induced Respiratory Depression

Description

An observational study will be conducted in approximately 14 participants to evaluate the ability of a wearable, wireless acoustic Respiratory Monitoring System (RMS) to accurately measure a participant's respiratory rate, tidal volume, minute ventilation, and duration of apnea in a noisy environment. Sensor accuracy will be measured with adaptive filtering and active noise cancellation turned on versus turned off.

Conditions

Respiratory Insufficiency, Clinical Deterioration

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Study Overview

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Study Details

Study overview

An observational study will be conducted in approximately 14 participants to evaluate the ability of a wearable, wireless acoustic Respiratory Monitoring System (RMS) to accurately measure a participant's respiratory rate, tidal volume, minute ventilation, and duration of apnea in a noisy environment. Sensor accuracy will be measured with adaptive filtering and active noise cancellation turned on versus turned off.

Wearable Wireless Respiratory Monitoring System That Detects and Predicts Opioid Induced Respiratory Depression

Wearable Wireless Respiratory Monitoring System That Detects and Predicts Opioid Induced Respiratory Depression

Condition
Respiratory Insufficiency
Intervention / Treatment

-

Contacts and Locations

Philadelphia

Thomas Jefferson University, Philadelphia, Pennsylvania, United States, 19107

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Age 18 to 70 years.
  • 2. BMI 20 to 38.
  • 3. Subject understands the English language, understands the risks, benefits, and alternatives to this research study, and is willing and able to give written informed consent.
  • 1. Age \<18 years\>70.
  • 2. BMI \< 20 or \> 38.
  • 3. Does not understand written and spoken English.
  • 4. Anxiety or claustrophobia related to wearing a face mask.
  • 5. History of skin irritation or inflammation related to the adhesive, adhesive tape, or materials used in the trachea sound sensor or facemask.
  • 6. Active infection or inflammation of the skin above the proximal trachea.
  • 7. Excessive facial hair that may prevent a tight seal around the facemask.
  • 8. Unstable cardiac, vascular, pulmonary, hepatic, renal, immune function at the discretion of the investigator.
  • 9. Pregnancy or breast feeding.
  • 10. Current participation in an industry sponsored pharmaceutical study or a medical device study.

Ages Eligible for Study

18 Years to 70 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Jeffrey Joseph,

Study Record Dates

2024-09-30