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Biospecimen DonationNCT06781424

University of Central Florida BEEAST

An observational study of Biospecimen Donation and Environmental Impact, run by University of Central Florida at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Since the inception of aerospace travel, NASA has been collecting biospecimens from professional astronauts for research. With the recent growth of civilian aerospace travelers, there is a need for biospecimen banking for civilian astronauts. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Biospecimen Donation, Environmental Impact
How many people
10,000 participants
Where
1 siteUnited States
Study dates
13 Jan 2025to 13 Jan 2075
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: The target population comprises of persons from many countries. Therefore, enrollees can be from other countries. However, biospecimen collection will occur in the USA.

Who may be able to join

  • Primary Enrollees: adults, ages 18 and older, and persons who travel (such as space travel) or live in extreme environments (such as Antarctica).
  • Secondary Enrollees: Referred adult family members (such as siblings and spouses) of primary enrollees.
  • Tertiary Enrollees: Adult persons from the general public can enroll to serve as matching controls. Tertiary enrollees will be screened based on age, gender, race and ethnicity, country of residence, disease/ conditions and employment history.
  • Pregnant women may choose to enroll.

Who cannot join

  • adults unable to consent,
  • minors (under age 18)
  • prisoners

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Britney-Ann Wray, BS, CTBS, CCRP contact

4072668742

britney-ann.wray@ucf.edu

United States1 site, 1 recruiting
  • University of Central Florida

    Orlando, Florida, 32827

    Britney-Ann Wray, BS, CTBS, CCRP, 4072668742, britney-ann.wray@ucf.edu

    Amoy Fraser, PhD, CCRP, PMP, 4072668742, amoy.fraser@ucf.edu

    Recruiting

Other trials in United States

About this study

Official title: University of Central Florida Biobank for Extreme Environments, Aviation and Space Travel

Since the inception of aerospace travel, NASA has been collecting biospecimens from professional astronauts for research. With the recent growth of civilian aerospace travelers, there is a need for biospecimen banking for civilian astronauts. This protocol addresses this gap by being a biobank for civilian astronauts, their family members (to be controls) and others who are also doing travel to extreme environments (pilots, submariners).

Read the detailed description

The objective of the University of Central Florida College of Medicine's Biobank for Extreme Environments, Aviation and Space Travel (BEEAST) is to acquire, store, and distribute identifiable human biospecimens and health information for medical research purposes only. The target population are astronauts, aviators, submariners, persons living in extreme environments (such as Antarctica), and their families, and people from the general population who can serve as matching controls.

Keywords
donate, biobank, biospecimen, astronaut, pilot

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT06781424
Study groupRoleWhat they receive
Primary PartcipantParticipants who have who travel (such as space travel) or live in extreme environments (such as Antarctica).
Secondary ParticipantParticipants who have been referred adult family members (such as siblings and spouses) of primary enrollees.
Tertiary PartcipantParticipants from the general public to serve as matching controls.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Receipt of donated biospecimen for aerospace research

    Donated biospecimens from participants will aid in the improvement of medical aerospace research. The key research divisions are cancer, cardiovascular, immunity and pathogenesis, neuroscience, and molecular microbiology.

    Measured: 50 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Jan 2025
  2. Study start13 Jan 2025
  3. Primary completion13 Jan 2075 (estimated)
  4. Study completion13 Jan 2075 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Other
Enrolment
10,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06781424
Sponsor's protocol ID
STUDY00007332
Status last verified
Mar 2025
First submitted
13 Jan 2025
Last updated
26 Mar 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Biospecimen Donation and Environmental Impact, run by University of Central Florida at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 26 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Britney-Ann Wray, BS, CTBS, CCRP (4072668742, britney-ann.wray@ucf.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Receipt of donated biospecimen for aerospace research (time frame: 50 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Mar 2025.

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