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How can I find funding opportunities (RFAs, RFPs and PAs)?
What do I need to know before submitting a clinical research application?
Am I a new investigator and what if this is my first NIH application?
Which NHLBI staff can help me?
Is my study considered clinical research?
Is my study observational or interventional?
What is the best award mechanism for my clinical research proposal?
What if my project exceeds $500,000 in direct costs in any given year?
Where can I get help with writing the application?
What must I include in Section E: Human Subjects Research?
How and when do I submit my application?

Glossary Box

 

Is my study observational or interventional?

Observational Study:
A biomedical or behavioral research study of human subjectsGlossary Term designed to assess risk factors for disease development or progression, assess natural history of risk factors or disease, identify variations based on geographic or personal characteristics (such as race/ethnicity or gender), track temporal trends, or describe patterns of clinical care and treatment in absence of specific study-mandated interventions.

Interventional Study:
For purposes of reviewing grant applications and contract proposals submitted to the NIH, a clinical trial is operationally defined as a prospective biomedical or behavioral research study of human subjects that is designed to answer specific questions about biomedical (drugs, treatments, devices, or new ways of using known drugs, treatments, or devices) or behavioral interventions. 
Clinical trials are used to determine whether new biomedical or behavioral interventions are safe, efficacious and effective. Clinical trials of experimental drug, treatment, device or behavioral intervention may proceed through four phases: 

  • Phase I Glossary Term
  • Phase II Glossary Term
  • Phase III Glossary Term (see also NIH-Defined Phase III Clinical TrialsGlossary Term)
  • Phase IV Glossary Term

 

 

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