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| Name | Class |
|---|---|
| Clayton Sleep Insititute | INDUSTRY |
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This study is designed to be a clinical validation study to ready the CPM System for FDA 510(k) submission. This study will be conducted as a prospective non-randomized. The study is non-significant risk since the CPM Device is noninterventional and noninvasive. The study is primarily designed to validate the accuracy of the respiration rate and the changes in relative tidal volume. All participants will be fitted with both the CPM Device as well as reference devices (capnography and ECG). Participants will be randomized between 4 procedures (A-D) which will determine the order of 10 exercises. Each exercise has about 2 minutes of device recording and two minutes of rest. Each exercise contains two positions: sitting up for one minute and lying down for one minute. For some exercises, the participant will be instructed to breathe at a certain rate (assisted by a metronome). For other exercises, the participants will breathe at a normal rate but change how deep the are breathing. For the last, all capnography reference devices will be removed, and an ECG reference device will be placed. After exercise 18, the participant will have all devices removed and the study visit will terminate. The participant will receive a safety follow-up call about 1 week after their visit.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Healthy Cohort | Experimental | The target population for this cohort is healthy adult volunteers who do not have preexisting heart or lung conditions or illness. The goal is to recruit a participant population with a range of body types and BMIs and an approximately even split of genders and compare the reference device measurements to the test device. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| CPM Device | Device | The CPM device and reference device are used simultaneous to validate the CPM device. |
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| Measure | Description | Time Frame |
|---|---|---|
| Accuracy of CPM System Calculated RR Versus Reference Device Via Percent of Error Accuracy of Respiration Rate | Percentage of respiration rate error within ± 2bpm. Acceptance criteria for clinical utility is >= 85%. The percentage of respiration rate within ± 2brpm was calculated by data points, regardless of its rate and breathing condition, which the CPM System did not screen, therefore reporting the numeric values. Each data point will produce binary result (True or False) if the error is within ± 2 brpm. Assuming this binary result follows a binominal distribution, its confidence interval is also calculated. | 90 minutes |
| Root Mean Squared Error (RMSE) of Respiration Rates From the CPM System vs Reference Device for Metronome Guided Breathing and Non-metronome Guided Breathing. | First, the subject-specific linear fitting is performed after taking the natural log of both CPM's rTV and reference TV. Then, the residual errors in rTV after the fitting were calculated. Finally, all subject's residual errors are pooled together to calculate the root mean squared (RMS) residual relative errors. The confidence interval was calculated assuming the square of this error follows Chi-square distribution. This error characterized in a log-log domain is converted back to characterize a relative accuracy by taking an exponential of natural constant followed by subtraction of one. The RMS of residual error in % is characterized in this way because the linear fitting in the log-log domain and its residual errors represents faithful relative residual error regardless of an absolute value of TV. | 90 minutes |
| Measure | Description | Time Frame |
|---|---|---|
| Performance of CPM System's ECG by % of CPM ECG Strip Equivalent to Lead II Strip | Performance of CPM System's ECG is measurement by comparing CPM System ECG metrics to the reference device Lead II ECG strip. Clinicians reviewed the criteria below and decided if the CPM strip had equivalence to the Lead II strip. | device measurement (3 minutes) |
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Inclusion Criteria:
Exclusion Criteria:
Injury or skin disturbance in the area of the test device
Allergies or sensitivities to silicone/acrylic-based adhesive
Pregnant
Currently smokes cigarettes
Has known respiratory conditions that might prevent them from following the study procedure such as:
Has self-reported heart or cardiovascular conditions such as chest pain, AFib, CHF, cardiomyopathy, or other conditions that could interfere with cardiopulmonary function
Has other self-reported health conditions that could interfere with the breathing patterns and exercises detailed in the protocol (including wearing a capnography mask)
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Clayton Sleep Institute | St Louis | Missouri | 63123 | United States |
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| ID | Title | Description |
|---|---|---|
| FG000 | Healthy Cohort | The target population for this cohort is healthy adult volunteers who do not have preexisting heart or lung conditions or illness. The goal is to recruit a participant population with a range of body types and BMIs and an approximately even split of genders and compare the reference device measurements to the test device. CPM Device: The CPM device and reference device are used simultaneous to validate the CPM device. |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
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| ID | Title | Description |
|---|---|---|
| BG000 | Healthy Cohort | The target population for this cohort is healthy adult volunteers who do not have preexisting heart or lung conditions or illness. The goal is to recruit a participant population with a range of body types and BMIs and an approximately even split of genders and compare the reference device measurements to the test device. CPM Device: The CPM device and reference device are used simultaneous to validate the CPM device. |
| Units | Counts |
|---|---|
| Participants |
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| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Accuracy of CPM System Calculated RR Versus Reference Device Via Percent of Error Accuracy of Respiration Rate | Percentage of respiration rate error within ± 2bpm. Acceptance criteria for clinical utility is >= 85%. The percentage of respiration rate within ± 2brpm was calculated by data points, regardless of its rate and breathing condition, which the CPM System did not screen, therefore reporting the numeric values. Each data point will produce binary result (True or False) if the error is within ± 2 brpm. Assuming this binary result follows a binominal distribution, its confidence interval is also calculated. | Posted | Number | 95% Confidence Interval | Percent | 90 minutes | device measurements | device measurements |
|
1 week
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Healthy Cohort | The target population for this cohort is healthy adult volunteers who do not have preexisting heart or lung conditions or illness. The goal is to recruit a participant population with a range of body types and BMIs and an approximately even split of genders and compare the reference device measurements to the test device. CPM Device: The CPM device and reference device are used simultaneous to validate the CPM device. |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Emily Wycallis | Analog Devices, Inc. | 9784351644 | emily.wycallis@analog.com |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | May 26, 2022 | Feb 22, 2024 | Prot_000.pdf |
| SAP | No | Yes | No | Statistical Analysis Plan | May 12, 2022 | May 14, 2024 | SAP_002.pdf |
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| ID | Term |
|---|---|
| D011660 | Pulmonary Heart Disease |
| ID | Term |
|---|---|
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
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Non-randomized control trial
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| ECG Accuracy Confirmation Comparing CPM Systems Generated ECG Metrics and Reference Lead II Generated ECG Metrics | Determine the accuracy of CPM System's ECG metrics to the reference device. Results are displayed as mean error with standard deviation of error. | device measurement (3 minutes) |
| years |
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| Sex: Female, Male | Count of Participants | Participants |
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| Ethnicity (NIH/OMB) | Count of Participants | Participants |
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| Race (NIH/OMB) | Count of Participants | Participants |
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| BMI | Mean | Standard Deviation | kg/m^2 |
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| Height | Mean | Standard Deviation | centimeters |
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| Weight | Mean | Standard Deviation | kilograms |
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| Upright Position |
This arm includes measurement data from position 2 of a CPM System reading (upright position). |
|
|
| Primary | Root Mean Squared Error (RMSE) of Respiration Rates From the CPM System vs Reference Device for Metronome Guided Breathing and Non-metronome Guided Breathing. | First, the subject-specific linear fitting is performed after taking the natural log of both CPM's rTV and reference TV. Then, the residual errors in rTV after the fitting were calculated. Finally, all subject's residual errors are pooled together to calculate the root mean squared (RMS) residual relative errors. The confidence interval was calculated assuming the square of this error follows Chi-square distribution. This error characterized in a log-log domain is converted back to characterize a relative accuracy by taking an exponential of natural constant followed by subtraction of one. The RMS of residual error in % is characterized in this way because the linear fitting in the log-log domain and its residual errors represents faithful relative residual error regardless of an absolute value of TV. | Posted | Number | breath rates per minute (BRPM) | 90 minutes | Device measurements | Device measurements |
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| Secondary | Performance of CPM System's ECG by % of CPM ECG Strip Equivalent to Lead II Strip | Performance of CPM System's ECG is measurement by comparing CPM System ECG metrics to the reference device Lead II ECG strip. Clinicians reviewed the criteria below and decided if the CPM strip had equivalence to the Lead II strip. | For 29 participants, a CPM lead strip and a Lead II ECG strip was generated. | Posted | Number | % of CPM Strips Equivalent to Lead II | device measurement (3 minutes) | ECG Strips | ECG Strips |
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| Secondary | ECG Accuracy Confirmation Comparing CPM Systems Generated ECG Metrics and Reference Lead II Generated ECG Metrics | Determine the accuracy of CPM System's ECG metrics to the reference device. Results are displayed as mean error with standard deviation of error. | For 29 participants, one ECG strip for CPM and one ECG strop for Lead II reference device were generated and compared. | Posted | Mean | Standard Error | milliseconds (ms) | device measurement (3 minutes) | ECG Strips | ECG Strips |
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| 0 |
| 40 |
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| 40 |
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| Title | Measurements |
|---|---|
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| QT interval measurability |
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| A-Fib Rhythm Readability |
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| Title | Measurements |
|---|---|
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| QT interval (ms) |
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| QT interval (ms) excluding 8% of outliers |
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| QTc interval |
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| QTc interval excluding 8% f outliers |
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