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Recruiting NCT06781424

University of Central Florida BEEAST

Observational Biospecimen Donation Environmental Impact

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Biospecimen Donation, Environmental Impact. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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).

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.

Primary outcome measures

  • Receipt of donated biospecimen for aerospace research [Time frame: 50 years]

Eligibility criteria

Inclusion criteria

  • 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.

Exclusion criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Other

Study locations

United States · 1 center
  • University of Central Florida — Orlando

Identifiers

NCT: NCT06781424 · STUDY00007332

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗