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| ID | Type | Description | Link |
|---|---|---|---|
| STUDY00011439/ ARS-2020-001 | Other Identifier | University of Washington Human Subjects Division |
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Study endpoints no longer feasible.
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| Name | Class |
|---|---|
| University of Washington | OTHER |
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The Apple Respiratory Study, a collaboration between researchers at Apple Inc. (the "Study Sponsor" or "Sponsor") and the Seattle Flu Study team at the University of Washington (UW) (the "UW Study Team"), is a prospective, longitudinal cohort, low risk Study to collect certain data from Apple Watch and iPhone to determine whether such data can detect physiologic and non-physiologic changes in individuals associated with respiratory illnesses due to influenza, SARS-CoV-2 and other respiratory pathogens (the "Study").
Initial Screening and Study enrollment will begin in 2021 among adults residing in the Greater Seattle area. Participants will be recruited and driven to the online Study Website managed by UW. If determined to be eligible following completion of the Prescreen Consent and an initial eligibility assessment via REDCap, potential participants will be asked to review and, if interested in participation, to complete the Main Study Consent via REDCap, as well as to engage in enrollment procedures across both REDCap and the Apple Research app. Redcap will be used for prescreening, enrollment survey, and kit activation survey. Participants will use the Apple Research app to complete onboarding surveys, weekly symptom surveys, illness follow-up surveys, and monthly lifestyle surveys. These surveys will help the investigators learn about onset of respiratory symptoms as well as sick contacts, flu and/or COVID-19 vaccination and risk factors for illness. Participants will also receive an Apple Watch to capture certain sensor data-which, along with iPhone sensor data, will be correlated with symptom onset and symptom trajectory. If a participant experiences an acute respiratory illness (ARI), defined as at least one respiratory symptom for at least 24 hours, that individual will be asked to complete a symptom onset survey and self-collect an anterior nasal swab, which will be sent to UW Laboratory Medicine for analysis. Participants will be able to access their COVID swab test results using a secure web portal. Additionally, individuals who test positive or inconclusive for SARS-CoV-2 will be notified via phone by the UW Study Team and given instructions as defined by and in accordance with state, local, and national public health guidance.
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| Measure | Description | Time Frame |
|---|---|---|
| Symptomatic individuals that self-report ARI and have a laboratory-confirmed positive test for SARS-CoV-2 and/or influenza within 72 hours | Proportion of symptomatic individuals that self-report ARI and have a laboratory-confirmed positive test for SARS-CoV-2 and/or influenza by self-swab within 72 hours of symptom onset. | Up to 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| Self-report ARI and positive test for SARS-CoV-2 and/or influenza within 7 days | Proportion of symptomatic individuals that self-report ARI and have a laboratory-confirmed positive test for SARS-CoV-2 and/or influenza by self-swab within 7 days of symptom onset. | Up to 6 months |
| Self-report ARI and test positive for other ARI within 7 days of symptom onset |
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Inclusion Criteria:
To participate in this Study, individuals must:
Exclusion Criteria:
To participate in this Study, individuals must not:
Individuals also may be excluded from the Study once target participant counts have been achieved for certain demographics, comorbidity groups, and/or residence based on zip code
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The Study aims to enroll up to 1000 adults. We estimate that we will detect approximately 70 laboratory confirmed influenza cases and 40 laboratory confirmed SARS-CoV-2 cases based on estimated event rate incidences.
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| Name | Affiliation | Role |
|---|---|---|
| Helen Chu, MD, MPH | University of Washington | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Washington | Seattle | Washington | 98109 | United States |
The individual study data will not be shared beyond the investigative team, and only available to the sponsor in coded form. These details are outlined in the study protocol.
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| ID | Term |
|---|---|
| D018352 | Coronavirus Infections |
| D007251 | Influenza, Human |
| ID | Term |
|---|---|
| D003333 | Coronaviridae Infections |
| D030341 | Nidovirales Infections |
| D012327 | RNA Virus Infections |
| D014777 | Virus Diseases |
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Proportion of symptomatic individuals that self-report ARI and test positive for another respiratory pathogen by self-swab within 7 days of symptom onset |
| Up to 6 months |
| Onset of ARI event | Onset of ARI event defined as date and time of first self-reported symptoms (Day 0) | Up to 6 months |
| Hand washing Sessions | Completed hand washing sessions per week as detected by Apple Watch | Up to 6 months |
| Measure of Heart Rate | Measure of Heart Rate in Heart Beats per minute | Up to 6 months |
| Measure of Heart Rate Variability | Measure of Heart Rate Variability in the standard deviation in the time interval between heart beats in milliseconds over variable periods of time. | Up to 6 months |
| Measure of Blood Oxygen | Measure of Blood oxygen or oxygen saturation -percentage of hemoglobin in your red blood cells carrying oxygen (taken from Apple Watch) | Up to 6 months |
| Nasal swab sample that returns with no pathogens (viral and bacterial) on the panel | Pathogen-negative ARI (pathogen not detected by laboratory testing; "pathogen negative ARI" could be due to chronic respiratory diseases, viral clearance, or inadequate sample collection) | Up to 6 months |
| RNaseP and viral CRT values | RNaseP and viral CRT values for laboratory-confirmed virus positive ARI episodes | Up to 6 months |
| Duration of viral shedding and viral loads | Duration of viral shedding and viral loads in COVID-positive patients as assessed by four swabs collected over two weeks of follow-up | Up to 6 months |
| ECG Reports | Wrist-based Electrocardiogram (ECG) from smart watch containing time-series representation of the measured voltage corresponding to heart function over 30 second measurement periods. | Up to 6 months |
| D007239 |
| Infections |
| D012141 | Respiratory Tract Infections |
| D009976 | Orthomyxoviridae Infections |
| D012140 | Respiratory Tract Diseases |