NIH staff help unlock secrets of vaccine immunity in nose and blood
NCT ID NCT04794829
First seen Jun 24, 2026 · Last updated Jul 31, 2026 · Updated 3 times
Summary
This study follows 150 NIH staff members for about a year to see how their immune systems respond to flu and COVID-19 vaccines. Participants give monthly blood and nasal samples to measure antibodies in both the body and the nose. The goal is to understand how long immunity lasts and how it works in different parts of the body. No vaccines are given as part of the study.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could help design better vaccines that protect both the body and the nose against flu and COVID-19.
- What could go wrong
- This is an observational study, not testing a new treatment. Results may not apply to the general public, and the small size (150 people) limits conclusions.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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75 people
The number who actually took part.
- Started
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Aug 2021
- Finished
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Jul 2026
- Lead sponsor
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A government research agency
The lead sponsor is the US National Institutes of Health.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
NIH staff may include employees and contractors, fellows, and volunteers.
- Ages
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18 to 120 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
* INCLUSION CRITERIA: In order to be eligible to participate in this study, an individual must meet all of the following criteria: 1. NIH staff members, at the time of enrollment. 2. Able to provide informed consent. 3. \>=18 years of age. 4. Planning to receive the current influenza season s vaccine and/or an FDA-authorized or approved SARS-CoV-2 vaccine. 5. Willing and able to undergo blood draws or home blood samplings and nasal sampling procedures. 6. Willing and able to undergo at least one blood draw and one nasal sampling prior to receiving vaccine. EXCLUSION CRITERIA: An individual who meets any of the following criteria will be excluded from participation in this study: 1. Already received the current season s influenza vaccine and does not plan to receive an FDA-authorized or approved SARS CoV-2 vaccine. 2. Already received an FDA-authorized or approved SARS-CoV-2 vaccine and does not plan to receive the current season s influenza vaccine. 3. Not willing to receive the current influenza season's vaccine and not willing to receive an FDA-authorized or approved SARS-CoV-2 vaccine. 4. Any condition that, in the opinion of the investigator, contraindicates participation in this study. Co-enrollment guidelines: Participants may be co-enrolled in other studies; however, study staff should be notified of co-enrollment.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
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Other studies related to the condition(s) this trial covers.
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