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Recruiting

NCT Number: NCT06958523

Apple Health Study

The Apple Health Study aims to build a diverse and inclusive group of participants to help researchers advance our understanding of how signals and information collected from apps and devices relate to health and may be used to predict, detect, monitor, and manage changes in health.

To enroll, US residents who have an iPhone can download the Apple Research app from the App Store and go through the introduction and informed consent for the Apple Health Study. This study is fully remote, and all are invited to enroll if the eligibility criteria are met.

Participants will be asked to complete tasks and surveys, using their iPhone and Apple Research app which include:

* Selecting the types of data they would like to share with the study such as health and sensor data * Completing tasks and surveys including areas such as personal demographic information, personal medical history, family history, and social determinants of health

Recruiting

Interested in participating?

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

MCRA, Washington D.C., District of Columbia, United States

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Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Be at least 18 years old (at least 19 years old in Alabama and Nebraska, at least 21 years old in Puerto Rico);
  • Live in the United States of America;
  • Have an iPhone;
  • Have installed Apple Research app on your iPhone;
  • Be comfortable communicating in written and spoken English;
  • Be willing and able to provide informed consent to participate in the Study.

Exclusion criteria

  • Share your iCloud account, iPhone, or devices that collect health data such as Apple Watch with anyone else, because it could result in sharing another person's health information with the Study, making it challenging for researchers to use your information.

Treatment and study plan

Primary outcomes

  1. Health Status

    Time frame: Baseline and every 6 months until study end (up to 5 years)

    Assessed by participant self-report as well as clinical health records and claims data. The initial count and change over time in the number and type of health conditions such as cardiovascular, circulatory, cognition, hearing, mental health, metabolic, mobility, neurologic, respiratory, sex and gender, reproduction, hormones, sleep, and health events such as hospitalizations, procedures or falls.

Secondary outcomes

  1. Participant Population: Demographic Characteristics of Study Participants

    Time frame: Baseline and annually until study end (up to 5 years)

    Results of surveys to report participant demographics.

  2. Social Determinants of Health: Lifestyle & Environment Survey

    Time frame: Baseline and every 6 months until study end (up to 5 years)

    Results of surveys that collect information about social determinants of health.

  3. Family Health History in Health Conditions and Health Events

    Time frame: Baseline and have option to update if needed (up to 5 years)

    Results of self-reported family health history of first-degree biologic family.

Study contacts

Contact information is provided by the study sponsor or research team.

MCRA Study Call Center

CONTACT

[email protected]

833-600-6993

Sponsors and collaborators

Lead sponsor

Apple Inc.

Industry

Collaborators

  • Brigham and Women's Hospital
  • MCRA

Registry information

Important dates

Study start
2025
Primary completion
2030
Study completion
2030
First posted
May 6, 2025
Registry last updated
Jul 29, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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