All of Us (initiative): Difference between revisions
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== All of Us (initiative) == | |||
The '''All of Us Research Program''' is a significant health research initiative launched by the [[National Institutes of Health]] (NIH) in the United States. The program aims to gather health data from one million or more people living in the United States to accelerate research and improve health outcomes. By collecting a diverse range of health information, the initiative seeks to enable individualized prevention, treatment, and care for people of all backgrounds. | |||
=== Objectives === | |||
The primary objectives of the All of Us Research Program include: | |||
* '''Diversity''': To reflect the diversity of the United States, the program aims to include participants from various [[ethnic groups]], [[age groups]], and [[socioeconomic backgrounds]]. | |||
* '''Precision Medicine''': To advance the field of [[precision medicine]], which involves tailoring medical treatment to the individual characteristics of each patient. | |||
* '''Research Resource''': To create a comprehensive research resource that can be used by researchers to study a wide range of health conditions and diseases. | |||
=== Data Collection === | |||
The All of Us initiative collects a variety of data types from its participants, including: | |||
* '''Electronic Health Records (EHRs)''': Participants' medical histories are collected to provide insights into their health over time. | |||
* '''Surveys''': Participants complete surveys about their lifestyle, environment, and health habits. | |||
* '''Physical Measurements''': Basic physical measurements such as height, weight, and blood pressure are recorded. | |||
* '''Biosamples''': Blood and urine samples are collected for [[genomic]] and other analyses. | |||
=== Participant Engagement === | |||
The program emphasizes participant engagement and transparency. Participants are considered partners in the research process and are kept informed about how their data is used. They also have access to their own health information and can learn about the research findings. | |||
=== Privacy and Security === | |||
Ensuring the privacy and security of participant data is a top priority for the All of Us Research Program. The program employs advanced security measures to protect data and follows strict protocols to ensure participant confidentiality. | |||
=== Impact === | |||
The All of Us Research Program is expected to have a significant impact on the future of healthcare by: | |||
* Enabling researchers to better understand the factors that contribute to health and disease. | |||
* Facilitating the development of new treatments and prevention strategies. | |||
* Promoting health equity by including underrepresented populations in research. | |||
== Related pages == | |||
* [[Precision medicine]] | |||
* [[National Institutes of Health]] | |||
* [[Genomics]] | |||
* [[Electronic health record]] | |||
{{National Institutes of Health}} | |||
{{Medicine}} | |||
[[Category:Medical research]] | |||
[[Category:National Institutes of Health]] | |||
[[Category:Health initiatives]] | |||
Latest revision as of 00:34, 19 February 2025
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All of Us (initiative)
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Stanford 2022 Wellness Fair
All of Us (initiative)[edit]
The All of Us Research Program is a significant health research initiative launched by the National Institutes of Health (NIH) in the United States. The program aims to gather health data from one million or more people living in the United States to accelerate research and improve health outcomes. By collecting a diverse range of health information, the initiative seeks to enable individualized prevention, treatment, and care for people of all backgrounds.
Objectives[edit]
The primary objectives of the All of Us Research Program include:
- Diversity: To reflect the diversity of the United States, the program aims to include participants from various ethnic groups, age groups, and socioeconomic backgrounds.
- Precision Medicine: To advance the field of precision medicine, which involves tailoring medical treatment to the individual characteristics of each patient.
- Research Resource: To create a comprehensive research resource that can be used by researchers to study a wide range of health conditions and diseases.
Data Collection[edit]
The All of Us initiative collects a variety of data types from its participants, including:
- Electronic Health Records (EHRs): Participants' medical histories are collected to provide insights into their health over time.
- Surveys: Participants complete surveys about their lifestyle, environment, and health habits.
- Physical Measurements: Basic physical measurements such as height, weight, and blood pressure are recorded.
- Biosamples: Blood and urine samples are collected for genomic and other analyses.
Participant Engagement[edit]
The program emphasizes participant engagement and transparency. Participants are considered partners in the research process and are kept informed about how their data is used. They also have access to their own health information and can learn about the research findings.
Privacy and Security[edit]
Ensuring the privacy and security of participant data is a top priority for the All of Us Research Program. The program employs advanced security measures to protect data and follows strict protocols to ensure participant confidentiality.
Impact[edit]
The All of Us Research Program is expected to have a significant impact on the future of healthcare by:
- Enabling researchers to better understand the factors that contribute to health and disease.
- Facilitating the development of new treatments and prevention strategies.
- Promoting health equity by including underrepresented populations in research.
Related pages[edit]
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