Toolkit.ncats.nih.gov

Clinical outcome

WEBClinical outcome. A clinical outcome is a measurable change in symptoms, overall health, ability to function, quality of life, or survival outcomes that result from giving care to …

Actived: 6 days ago

URL: https://toolkit.ncats.nih.gov/glossary/clinical-outcome/

Personally identifiable information

WEBPersonally identifiable information (PII) refers to information that can be used to distinguish or trace an individual’s identity, either alone (direct) or when combined with other …

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Benefits of Guidelines

WEBBenefits include: Provides evidence-based clinical guidance. The level of evidence for each recommendation is included. Strength of a specific recommendation is also rated and …

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Consent Requirements

WEBConsent Requirements. The goal of informed consent for clinical trials is to make sure participants are fully aware of all aspects of the research study from their perspective. …

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Cell and Animal Models

WEBCell and Animal Models. A disease model is an animal or cell which displays all or some of the disease processes that are observed in the actual human.. Studying disease models …

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Patient advocate

WEBPatient advocate. An individual or group of individuals, who may or may not be part of the target patient population, who has a role in promoting an interest or cause to influence …

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Patient preference information

WEBPatient preference information (PPI) refers to assessments of the relative desirability or acceptability to patients of specified alternatives or choices among outcomes or other …

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FDA Surveillance Programs

WEBFDA Surveillance Programs. The FDA has several policies and programs in place that are intended to promote appropriate postmarket surveillance. Understanding these …

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Protected personally identifiable information

WEBProtected personally identifiable information (Protected PII) refers to an individual’s first name or first initial and last name in combination with any one or more of types of …

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Patient perspective

WEBPatient perspective refers to a type of patient experience data that specifically relates to patients’ attitudes or points of view about their condition or its management. Patient …

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Keeping Up with Advances

WEBKeeping Up with Advances. Keeping up with new therapeutic approaches and technologies can be time consuming. However, there are resources that provide summaries and …

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List of NIH Institutes, Centers, and Offices

WEBMaintained by the National Center for Advancing Translational Sciences (NCATS)

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De-identified patient data

WEBDe-identified patient data is patient information that has had personally identifiable information (PII; e.g. a person’s name, email address, or social security number), …

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Research versus Clinical Care

WEBClinical care setting, no research involved: Provides care that is in the best interest of the patient. Addresses the needs of individual patients. Makes real-time decisions about …

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