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Search / Trial NCT04856410

Effects of Long-Duration Spaceflight on General and Spatial Cognition and Its Neural Basis

Launched by UNIVERSITY OF PENNSYLVANIA · Apr 19, 2021

Trial Information

Current as of June 26, 2025

Enrolling by invitation

Keywords

Astronauts Spaceflight Cognition Long Duration Spaceflight

ClinConnect Summary

This is an international proposal consisting of two projects with synergistic aims that will be carried out in a joint effort by the National Aeronautics and Space Administration (NASA) and the German Aerospace Center (DLR) as well as the European Space Agency (ESA). The project targets NASA's particular interest in studying the 'Cognitive-perceptual-visuospatial brain domain changes due to isolation and confinement' as part of the Complement of Integrated Protocols for Human Exploration Research (CIPHER) project on the International Space Station (ISS). The collected data will demonstrate ...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Astronauts (according to NASA requirements)
  • 2. Normal, healthy volunteers (astronaut surrogates) - Astronaut surrogates will be matched for sex, age and education relative to astronauts
  • Exclusion Criteria:
  • For astronauts and normal, healthy volunteers (astronaut surrogates):
  • 1. Subjects that do not comply with the MRI testing requirements. The following and other conditions may exclude the subject from MRI scanning or require additional examination to assess specific contraindications:
  • Tinnitus;
  • Sensori-neural hearing loss \> 30 decibels (dB);
  • Pace-maker or internal defibrillator;
  • metallic implants (e.g. orthopedic plates after bone fractures, joint replacements, surgical staples or clips, artificial heart valves, stents, cava filters);
  • Metallic splinters (e.g. after an accident or due to war injury);
  • Non-removable dental brace;
  • Intrauterine contraceptive devices (IUD) that are not MRI-compatible;
  • Cochlear implant (implanted hearing device);
  • Medication pump;
  • Acupuncture needle;
  • Other foreign bodies/objects which are non-removable;
  • Pregnancy (or its possibility);
  • Previous brain and/or heart surgery.
  • Tattoos and/or permanent make-up in the body (some inks contain metallic particles).
  • 2. Female subjects in this study are either astronauts or will model those in the astronaut population for whom participation in space missions is not allowed during pregnancy.

About University Of Pennsylvania

The University of Pennsylvania, a prestigious Ivy League institution located in Philadelphia, is renowned for its commitment to advancing medical research and improving healthcare outcomes. As a clinical trial sponsor, the university leverages its extensive resources, interdisciplinary expertise, and cutting-edge facilities to conduct innovative studies across various therapeutic areas. With a focus on translating scientific discoveries into clinical applications, the University of Pennsylvania fosters collaborations among leading researchers, clinicians, and industry partners, ensuring rigorous trial design and adherence to ethical standards. Through its dedication to excellence in research and education, the university plays a pivotal role in shaping the future of medicine.

Locations

Berlin, , Germany

Philadelphia, Pennsylvania, United States

Houston, Texas, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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