Privacy is a growing concern in mobile health research, particularly regarding passive data. Apple SensorKit provides a novel platform for collecting phone and wearable usage and sensor data, however the acceptability and feasibility of collecting these sensitive data to research subjects remains unknown. We piloted the SensorKit platform with a large sample of first-year U.S. medical residents as part of the longitudinal Intern Health Study. Findings demonstrate that successful enrollment and retention rates can be achieved in a longitudinal e-Cohort study that collects SensorKit data, however lower opt-in rates among racial minorities suggest the need for further evaluation of the equity implications around specific data types in mobile health research.

The authors have declared no competing interest.

This study received funding from the National Institutes of Health (R01MH101459).

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

The study design was approved by the Institutional Review Board at the University of Michigan and the participating hospitals in the Intern Health Study (HUM00033029).

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

All data produced in the present study are available upon reasonable request to the authors