Wearable Data for Personalized Prognostication in Cancer: A Registry Protocol

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCity of Hope Medical Center

About this trial

This study receives physiological and lifestyle-related data from mobile phones to create an institutional database.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age: ≥ 18 years

Has Apple Health app on personal device with valid iOS operating software (i.e., iOS 15.0 or higher)

Has a registered MyChart/MyCityofHope account (or be willing to register for one) and the app downloaded onto the personal device that also contains the Apple Health app with their data

Ability to read and understand English to review MyChart/MyCityofHope on-screen instructions to sync and share Apple Health data

Disqualifiers

Prospective participants who, in the opinion of the investigator, may not be able to comply with all study procedures (including compliance issues related to feasibility/logistics)

City of Hope employees listed on the study roster or who manage employees listed on the study roster

Trial population

Patients and employees at City of Hope MedicalCenter that own an apple mobile device.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Non-Interventional Study

    Other intervention

    Non-Interventional Study

Treatment groups

1,200 Participants
are divided into 1 treatment group
Group A: Observational1 intervention

Trial outcomes

Primary outcomes

1

Feasibility of data collection

The proportion of participants for whom a successful data connection is established between their Apple Health data and the study registry will be quantified". Then for each variable captured by Apple Health, we will quantify the following feasibility metrics for data collection, evaluated separately for the retrospective (up to 8 years) and prospective (up to 5 years) data periods: For each subject, the total amount of retrospective (and prospective) HealthKit data available per patient in days and months will be calculated. For each subject, the number of days per week that a variable is available will be estimated and summarized by the average and standard deviation across weeks (or months). For both 1-2, the metrics will be calculated when pooling all available data, and separately for windows of 6 months. We will examine histograms and boxplots of the distributions across the cohort.

Time frame
Up to 8.5 years

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: