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Wearable near-infrared neuroimaging and task performance for brain function during an Antarctic winter-over

Wearable near-infrared neuroimaging and task performance for brain function during an Antarctic winter-over - Winterbrain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00034218
Enrollment
45
Registered
2024-06-04
Start date
2024-08-08
Completion date
Unknown
Last updated
2026-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neurophysiological basics of operational performance

Interventions

Group 1: Isolation group: Wintering at Concordia Station in the Antarctic Group 2: Control group: carries out the study protocol on an outpatient basis in Cologne

Sponsors

Deutsches Zentrum für Luft und Raumfahrt - Institut für Luft- und Raumfahrtmedizin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: - Naïve to 6df spacecraft docking or similar tasks - No history of head injury or other neurological or psychiatric disorders - No history of cardiac disease, including ischemic heart disease, arrhythmia, hypertension, or syncope - Not taking any drugs known to effect neural or cardiovascular function - Ability to give a written and dated informed consent

Exclusion criteria

Exclusion criteria: - Current illegal drug use - Alcohol abuse - Participation in previous studies involving performance of 6df spacecraft docking or similar tasks

Design outcomes

Primary

MeasureTime frame
The primary endpoints are the performance and progress of the learning process in a complex manual control task (docking simulation). In addition to the time course (one measurement x months before, x monthly measurements during and one measurement x months after the isolation/main phase of the study), the comparison between the isolation group and the control group is also considered in order to identify possible deficits under isolation conditions. The accompanying measurements with the NinScan device (ECG, EEG, fNIRS) will be used to identify physiological correlates of operational performance and physiological changes under isolation.

Secondary

MeasureTime frame
Correlation of physiological and performance data with other variables: In the isolation group, hair and saliva samples are collected to determine cortisol, dehydroepiandrosterone, endocannabinoids and viral load, and data collected on Concordia as part of the Isolation Standard Measures are used (e.g. actigraphy to characterize sleep, questionnaires on mood, sleep, health and stress). In both groups, a short questionnaire with questions on sleep, mood and motivation is collected. In the control group, eye movements are also recorded using an eye tracker and associated with performance in the 6df simulation. In addition, cognitive performance is also assessed using a computerized oculomotor test battery and enables the correlation of docking performance with cognitive and sensorimotor abilities.

Countries

Germany

Contacts

Public ContactEdwin Mulder

Deutsches Zentrum für Luft- und Raumfahrt - Institut für Luft- und Raumfahrtmedizin

edwin.mulder@dlr.de+49 2203 601 3062

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 27, 2026