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Measuring cognitive functioning during hypoxia with near infrared spectroscopy and electro encephalography

Measuring cognitive functioning during hypoxia with near infrared spectroscopy and electro encephalography - Cognitive functioning and hypoxia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON33270
Enrollment
18
Registered
2009-02-11
Start date
2009-06-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

functioneren onder hypoxie hypoxia insufficient oxygen

Interventions

Partly deoxygenated air will be inhaled by the subjects with a special breathing mask. Oxygen saturation levels will be manipulated and actively kept constant at (1) 98%, baseline sea level, (2) 90%

Sponsors

TNO
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Non smoking, or stopped at least 1 years ago. 2. Aged between 18 and 30 years, at day 01 of the study. 3. Apparently healthy based on the anamnesis (see appendix). 4. Having given their written informed consent. 5. Wiling to comply with the study procedures. 6. Willing to accept use of all anonymous data, including publication, and the confidential use and storage of all data. 7. Willing to accept the disclosure of the financial benefit of participation in the study to the authorities concerned.

Exclusion criteria

Exclusion criteria: 1.Medical problems (amongst others, cardiovascular and respiratory diseases). 2.No use of prescribed medication in the last 14 days prior to start of the study, with the exception of the use of aspirins and ibuprofen and oral contraceptives (o.a.c.). These can be taken until 72 hours prior to the start (this does not apply for o.a.c.) . 3.Use of drugs. 4.Sickness in the last 7 days prior to the start of the study. 5.Not willing to except the transfer of relevant study results to their physician. 6.Having donated blood in the last 14 days

Design outcomes

Primary

MeasureTime frame
The main study parameters are cognitive functioning (working memory, tracking, vigilance, planning), blood oxygen saturation levels (cerebral), brain activity of the frontal cortex, heart rate and blood pressure.

Secondary

MeasureTime frame
peripheral oxygen saturation levels, heart rate and blood pressure.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)