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Project Title:  Evaluation of Photic Countermeasures for Circadian Entrainment of Neurobehavioral Performance and Sleep-Wake Regulation Before and During Spaceflight Reduce
Fiscal Year: FY 2012 
Division: Human Research 
Research Discipline/Element:
HRP BHP:Behavioral Health & Performance (archival in 2017)
Start Date: 05/01/2008  
End Date: 09/30/2012  
Task Last Updated: 01/08/2013 
Download Task Book report in PDF pdf
Principal Investigator/Affiliation:   Czeisler, Charles A. M.D., Ph.D. / Brigham and Women's Hospital/Harvard Medical Center 
Address:  Division of Sleep Medicine 
221 Longwood Ave., Ste. 438 
Boston , MA 02115-5804 
Email: caczeisler@rics.bwh.harvard.edu 
Phone: 617-732-4013  
Congressional District:
Web:  
Organization Type: UNIVERSITY 
Organization Name: Brigham and Women's Hospital/Harvard Medical Center 
Joint Agency:  
Comments:  
Co-Investigator(s)
Affiliation: 
Barger, Laura  Brigham and Women's Hospital 
Aeschbach, Daniel  Brigham and Women's Hospital 
Project Information: Grant/Contract No. NCC 9-58-HFP01601 
Responsible Center: NSBRI 
Grant Monitor:  
Center Contact:   
Unique ID: 7045 
Solicitation / Funding Source: 2007 Crew Health NNJ07ZSA002N 
Grant/Contract No.: NCC 9-58-HFP01601 
Project Type: Ground 
Flight Program:  
TechPort: Yes 
No. of Post Docs:
No. of PhD Candidates:
No. of Master's Candidates:
No. of Bachelor's Candidates: 33 
No. of PhD Degrees:
No. of Master's Degrees:
No. of Bachelor's Degrees: 28 
Human Research Program Elements: (1) BHP:Behavioral Health & Performance (archival in 2017)
Human Research Program Risks: None
Human Research Program Gaps: None
Task Description: To synchronize astronauts' circadian sleep-wake schedules to variable launch times, timed exposure to bright light and darkness in the crew quarters during the week-long pre-launch quarantine period has been used since 1990. Although successful at circadian entrainment, bright light protocols are complex to administer and astronauts' compliance is compromised because bright light glare compromises screen visibility, and increases frequency of headaches, irritability, and nausea. Moreover, bright light remains unavailable as an in-flight countermeasure, requiring astronauts to rely upon hypnotics or wake-promoting therapeutics to provide symptomatic relief. Recent advances reveal that the human circadian pacemaker is most sensitive to shorter wavelength light for both phase shifting and direct enhancement of alertness and performance. We therefore proposed to test the efficacy of exposure to short wavelength green light at a standard intensity for pre-launch and in-flight phase shifting.

To this end, we examined the circadian phase-shifting efficacy of exposure to short wavelength light throughout scheduled wake times on a protocol designed to simulate the schedule of crew members during the pre-launch quarantine period on a mission that requires an 8h phase advance of the sleep-wake schedule. Our goal was to demonstrate that exposure to ambient short wavelength fluorescent light would synchronize human circadian rhythms to a shifted sleep/wake schedule within 4-5 days, enhancing alertness and performance during the biological night.

During this proposed simulation sleep-wake schedules were advanced by 8h using 3 different schedule protocol designs: 1) a "slam" shift in which the sleep episode was abruptly advanced by 8h and then maintained for 4 days, 2) a gradual shift in which the sleep episode was advanced by 1.6h each day for 5 days until an 8h advance was achieved, and 3) a slam shift with naps in which the extended wake period prior to the 8h advance of the sleep period included 2 short nap opportunities. Given the prolonged extended wake period on the second day of the slam shift schedule, the new schedule involved the opportunity to obtain two short naps: one for 2h during the afternoon circadian dip, and the second for 4h at the circadian nadir during the night. A total of 43 participants were studied in the project. They were randomized to 1 of 5 protocol conditions which differed by light and by shift schedule. The 5 conditions were 1) white light slam shift, 2) green light slam shift, 3) combined white + green light slam shift with naps, 4) white light gradual shift, and 5) green light gradual shift.

Our specific aims were to test the hypotheses that: 1. Exposure to ambient polychromatic green light would be more effective than exposure to an equal illuminance of polychromatic white in shifting circadian rhythms, as measured by dim-light melatonin onset (DLMO), in response to both a gradual 8h advance and to an abrupt shift of their sleep-wake schedule. 2. Alertness and neurobehavioral performance in dim light on a constant routine (CR) during times at which crew members should be awake on the simulated mission would be significantly greater following 4-5 days of exposure to ambient polychromatic green light vs. ambient white light of equal illuminance, due to more effective circadian entrainment. 3. Alertness and neurobehavioral performance would be significantly better on the first night of exposure to ambient polychromatic short wavelength light vs. ambient white light of equal illuminance, prior to the induced circadian phase shifts, due to the immediate alerting effects of exposure to ambient polychromatic short wavelength light. 4. Sleep efficiency and total sleep time would be significantly increased and latency to persistent sleep and wake time after sleep onset would be significantly decreased during the sleep episode following 4-5 days of exposure to ambient polychromatic green light vs. ambient white light of equal illuminance, due to more effective circadian entrainment.

We predicted that exposure to polychromatic green light throughout the day would rapidly entrain the circadian melatonin rhythm to the shifted sleep-wake schedule. We also predicted that green light combined with brighter white to prevent the altered color-perception from the green light alone would enable implementation of this new technology to ensure circadian synchronization both during the pre-flight quarantine period and while aboard NASA flight vehicles. We predicted that our new schedule with naps would reduce the excessive daytime sleepiness and other adverse effects often experienced with the slam shift due to prolonged wakefulness. As per a supplemental grant (HPF00003), we implemented novel infra-red reflectance oculography technology into this protocol to detect fatigue, and collected data on eye movements in n=30 participants during periods of extended wake. New eye tracking technologies were implemented into the protocol, in order to examine causes of neurobehavioral deficits during periods of extended wake.

Research Impact/Earth Benefits: We implemented and tested a new polychromatic fluorescent lamp with a peak spectral sensitivity of ~500 nm. This is near the peak sensitivity of the human circadian system, and thus should be the most efficacious polychromatic lamp for shifting the timing of the human biological clock. In addition to benefits for NASA flight personnel this technology will also have application to shift-workers, to jet travelers, and to any personnel who need to shift the timing of their biological rhythms.

Task Progress & Bibliography Information FY2012 
Task Progress: In the last year we completed our in-patient studies ahead of schedule. We also implemented novel infra-red reflectance oculography technology into this protocol for detecting fatigue, and collected data on eye movements in n=30 participants during periods of extended wake. We have completed analysis of melatonin assay results, and are continuing analysis of sleep, alertness, performance testing, and eye movement data; we also are preparing manuscripts of results.

Bibliography: Description: (Last Updated: 11/17/2025) 

Show Cumulative Bibliography
 
Articles in Peer-reviewed Journals Czeisler CA. "Medical and genetic differences in the adverse impact of sleep loss on performance: ethical considerations for the medical profession." Trans Am Clin Climatol Assoc. 2009;120:249-85. Review. PubMed PMID: 19768182 , Nov-2009
Articles in Peer-reviewed Journals Anderson C, Sullivan JP, Flynn-Evans EE, Cade BE, Czeisler CA, Lockley SW. "Deterioration of neurobehavioral performance in resident physicians during repeated exposure to extended duration work shifts." Sleep. 2012 Aug 1;35(8):1137-46. http://dx.doi.org/10.5665/sleep.2004 ; PubMed PMID: 22851809 , Aug-2012
Articles in Peer-reviewed Journals Buxton OM, Cain SW, O'Connor SP, Porter JH, Duffy JF, Wang W, Czeisler CA, Shea SA. "Adverse metabolic consequences in humans of prolonged sleep restriction combined with circadian disruption." Sci Transl Med. 2012 Apr 11;4(129):129ra43. http://dx.doi.org/10.1126/scitranslmed.3003200 ; PubMed PMID: 22496545 , Apr-2012
Articles in Peer-reviewed Journals Cain SW, Dennison CF, Zeitzer JM, Guzik AM, Khalsa SB, Santhi N, Schoen MW, Czeisler CA, Duffy JF. "Sex differences in phase angle of entrainment and melatonin amplitude in humans." J Biol Rhythms. 2010 Aug;25(4):288-96. http://dx.doi.org/10.1177/0748730410374943 ; PubMed PMID: 20679498 , Aug-2010
Articles in Peer-reviewed Journals Chang AM, Scheer FA, Czeisler CA. "The human circadian system adapts to prior photic history." J Physiol. 2011 Mar 1;589(Pt 5):1095-102. Epub 2011 Jan 10. http://dx.doi.org/10.1113/jphysiol.2010.201194 ; PubMed PMID: 21224217 , Mar-2011
Articles in Peer-reviewed Journals Dijk DJ, Duffy JF, Silva EJ, Shanahan TL, Boivin DB, Czeisler CA. "Amplitude reduction and phase shifts of melatonin, cortisol and other circadian rhythms after a gradual advance of sleep and light exposure in humans." PLoS One. 2012;7(2):e30037. Epub 2012 Feb 17. http://dx.doi.org/10.1371/journal.pone.0030037 ; PubMed PMID: 22363414 , Feb-2012
Articles in Peer-reviewed Journals Duffy JF, Cain SW, Chang AM, Phillips AJK, Munch MY, Gronfier C, Wyatt JK, Dijk D-J, Wright KP Jr, Czeisler CA. "Sex difference in the near-24-hour intrinsic period of the human circadian timing system." Proc Natl Acad Sci U S A. 2011 Sep 13;108 Suppl 3:15602-8. Epub 2011 May 2. http://dx.doi.org/10.1073/pnas.1010666108 ; PubMed PMID: 21536890 , Sep-2011
Articles in Peer-reviewed Journals Gooley JJ, Chamberlain K, Smith KA, Khalsa SB, Rajaratnam SM, Van Reen E, Zeitzer JM, Czeisler CA, Lockley SW. "Exposure to room light before bedtime suppresses melatonin onset and shortens melatonin duration in humans." J Clin Endocrinol Metab. 2011 Mar;96(3):E463-72. Epub 2010 Dec 30. http://dx.doi.org/10.1210/jc.2010-2098 ; PubMed PMID: 21193540 , Mar-2011
Articles in Peer-reviewed Journals Gooley JJ, Ho Mien I, St Hilaire MA, Yeo SC, Chua EC, van Reen E, Hanley CJ, Hull JT, Czeisler CA, Lockley SW. "Melanopsin and rod-cone photoreceptors play different roles in mediating pupillary light responses during exposure to continuous light in humans." J Neurosci. 2012 Oct 10;32(41):14242-53. http://dx.doi.org/10.1523/JNEUROSCI.1321-12.2012 ; PubMed PMID: 23055493 , Oct-2012
Articles in Peer-reviewed Journals Gooley JJ, Rajaratnam SM, Brainard GC, Kronauer RE, Czeisler CA, Lockley SW. "Spectral responses of the human circadian system depend on the irradiance and duration of exposure to light." Sci Transl Med. 2010 May 12;2(31):31ra33. http://dx.doi.org/10.1126/scitranslmed.3000741 ; PubMed PMID: 20463367 , May-2010
Articles in Peer-reviewed Journals Jung CM, Ronda JM, Czeisler CA, Wright KP Jr. "Comparison of sustained attention assessed by auditory and visual psychomotor vigilance tasks prior to and during sleep deprivation." J Sleep Res. 2011 Jun;20(2):348-55. Epub 2010 Aug 31. http://dx.doi.org/10.1111/j.1365-2869.2010.00877.x ; PubMed PMID: 20819145 , Jun-2011
Articles in Peer-reviewed Journals Klerman EB, Wang W, Duffy JF, Dijk DJ, Czeisler CA, Kronauer RE. "Survival analysis indicates that age-related decline in sleep continuity occurs exclusively during NREM sleep." Neurobiol Aging. 2013 Jan;34(1):309-18. Epub 2012 Jun 23. http://dx.doi.org/10.1016/j.neurobiolaging.2012.05.018 ; PubMed PMID: 22727943 , Jan-2013
Articles in Peer-reviewed Journals Rüger M (also Ruger M for searching purposes), St Hilaire MA, Brainard GC, Khalsa SB, Kronauer RE, Czeisler CA, Lockley SW. "Human phase response curve to a single 6.5-h pulse of short-wavelength light." J Physiol. 2013 Jan 1;591(Pt 1):353-63. Epub 2012 Oct 22. http://dx.doi.org/10.1113/jphysiol.2012.239046 ; PubMed PMID: 23090946 , Jan-2013
Articles in Peer-reviewed Journals Santhi N, Aeschbach D, Horowitz TS, Czeisler CA. "The impact of sleep timing and bright light exposure on attentional impairment during night work." J Biol Rhythms. 2008 Aug;23(4):341-52. http://dx.doi.org/10.1177/0748730408319863 ; PubMed PMID: 18663241 , Aug-2008
Articles in Peer-reviewed Journals St Hilaire MA, Gooley JJ, Khalsa SB, Kronauer RE, Czeisler CA, Lockley SW. " Human phase response curve to a 1 h pulse of bright white light." J Physiol. 2012 Jul 1;590(Pt 13):3035-45. Epub 2012 Apr 30. http://dx.doi.org/10.1113/jphysiol.2012.227892 ; PubMed PMID: 22547633 , Jul-2012
Articles in Peer-reviewed Journals Chang AM, Scheer FA, Czeisler CA, Aeschbach D. "Direct effects of light on alertness, vigilance, and the waking electroencephalogram in humans depend on prior light history." Sleep. 2013 Aug 1;36(8):1239-46. http://dx.doi.org/10.5665/sleep.2894 ; PubMed PMID: 23904684 , Aug-2013
Articles in Peer-reviewed Journals Rahman SA, Flynn-Evans EE, Aeschbach D, Brainard GC, Czeisler CA, Lockley SW. "Diurnal spectral sensitivity of the acute alerting effects of light." Sleep. 2014 Feb 1;37(2):271-81. http://dx.doi.org/10.5665/sleep.3396 ; PubMed PMID: 24501435; PubMed Central PMCID: PMC3900613 , Feb-2014
Articles in Peer-reviewed Journals Chang A, Aeschbach D, Duffy JF, Czeisler CA. "Evening use of light-emitting eReaders negatively affects sleep, circadian timing, and next-morning alertness." Proc Natl Acad Sci U S A. 2015 Jan 27;112(4):1232-7. Epub 2014 Dec 22. http://dx.doi.org/10.1073/pnas.1418490112 ; PubMed PMID: 25535358; PubMed Central PMCID: PMC4313820 , Jan-2015
Articles in Peer-reviewed Journals Wright KP Jr, Drake AL, Frey DJ, Fleshner M, Desouza CA, Gronfier C, Czeisler CA. "Influence of sleep deprivation and circadian misalignment on cortisol, inflammatory markers, and cytokine balance." Brain Behav Immun. 2015 Jul;47:24-34 .Epub 2015 Jan 29. http://dx.doi.org/10.1016/j.bbi.2015.01.004 ; PubMed PMID: 25640603 , Jul-2015
Articles in Peer-reviewed Journals Chang AM, Czeisler CA. "Reply to Zeitzer: Good science, in or out of the laboratory, should prevail." Proc Natl Acad Sci U S A. 2015 Mar 31;112(13):E1514. http://dx.doi.org/10.1073/pnas.1501544112 ; PubMed PMID: 25762077; PubMed Central PMCID: PMC4386345 , Mar-2015
Articles in Peer-reviewed Journals Chang AM, Bjonnes AC, Aeschbach D, Buxton OM, Gooley JJ, Anderson C, Van Reen E, Cain SW, Czeisler CA, Duffy JF, Lockley SW, Shea SA, Scheer FA, Saxena R. "Circadian gene variants influence sleep and the sleep electroencephalogram in humans." Chronobiol Int. 2016;33(5):561-73. Epub 2016 Apr 18. http://dx.doi.org/10.3109/07420528.2016.1167078 ; PubMed PMID: 27089043 , Apr-2016
Articles in Peer-reviewed Journals Lane JM, Chang AM, Bjonnes AC, Aeschbach D, Anderson C, Cade BE, Cain SW, Czeisler CA, Gharib SA, Gooley JJ, Gottlieb DJ, Grant SF, Klerman EB, Lauderdale DS, Lockley SW, Munch M, Patel S, Punjabi NM, Rajaratnam SM, Rueger M, St Hilaire MA, Santhi N, Scheuermaier K, Van Reen E, Zee PC, Shea SA, Duffy JF, Buxton OM, Redline S, Scheer FA, Saxena R. "Impact of common diabetes risk variant in MTNR1B on sleep, circadian, and melatonin physiology." Diabetes. 2016 Jun;65(6):1741-51. Epub 2016 Feb 11. http://dx.doi.org/10.2337/db15-0999 ; PubMed PMID: 26868293; PubMed Central PMCID: PMC4878414 , Jun-2016
Articles in Peer-reviewed Journals Cain SW, Chang AM, Vlasac I, Tare A, Anderson C, Czeisler CA, Saxena R. "Circadian rhythms in plasma brain-derived neurotrophic factor differ in men and women." J Biol Rhythms. 2017 Feb;32(1):75-82. https://doi.org/10.1177/0748730417693124 ; PubMed PMID: 28326910 , Feb-2017
Articles in Peer-reviewed Journals Grant LK, Cain SW, Chang AM, Saxena R, Czeisler CA, Anderson C. "Impaired cognitive flexibility during sleep deprivation among carriers of the Brain Derived Neurotrophic Factor (BDNF) Val66Met allele." Behav Brain Res. 2018 Feb 15;338:51-5. Epub 2017 Sep 22. https://doi.org/10.1016/j.bbr.2017.09.025 ; PubMed PMID: 28947280 , Feb-2018
Articles in Peer-reviewed Journals Chang AM, Duffy JF, Buxton OM, Lane JM, Aeschbach D, Anderson C, Bjonnes AC, Cain SW, Cohen DA, Frayling TM, Gooley JJ, Jones SE, Klerman EB, Lockley SW, Munch M, Rajaratnam SMW, Rueger M, Rutter MK, Santhi N, Scheuermaier K, Van Reen E, Weedon MN, Czeisler CA, Scheer F, Saxena R. "Chronotype genetic variant in PER2 is associated with intrinsic circadian period in humans." Sci Rep. 2019 Mar 29;9(1):5350. Published online 29 March 2019. https://doi.org/10.1038/s41598-019-41712-1 ; PubMed PMID: 30926824; PubMed Central PMCID: PMC6440993 , Mar-2019
Articles in Peer-reviewed Journals Swanson CM, Kohrt WM, Wolfe P, Wright KP Jr, Shea SA, Cain SW, Munch M, Vujovic N, Czeisler CA, Orwoll ES, Buxton OM. "Rapid suppression of bone formation marker in response to sleep restriction and circadian disruption in men." Osteoporosis Int. 2019 Dec;30(12):2485-93. Epub 2019 Aug 24. https://doi.org/10.1007/s00198-019-05135-y ; PubMed PMID: 31446439; PMCID: PMC6879850 [reported originally as Online first 2019 Aug 24] , Dec-2019
Articles in Peer-reviewed Journals St Hilaire MA, Anderson C, Anwar J, Sullivan JP, Cade BE, Flynn-Evans EE, Czeisler CA, Lockley SW; Harvard Work Hours Health and Safety Group. "Brief (<4 hour) sleep episodes are insufficient for restoring performance in first-year resident physicians working overnight extended-duration work shifts." Sleep. 2019 May 1;42(5):zsz041. https://doi.org/10.1093/sleep/zsz041 ; PubMed PMID: 30794317; PubMed Central PMCID: PMC6519906 , May-2019
Articles in Peer-reviewed Journals Swanson CM, Shea SA, Kohrt WM, Wright KP, Cain SW, Munch M, Vujovic N, Czeisler CA, Orwoll ES, Buxton OM. "Sleep restriction with circadian disruption negatively alter bone turnover markers in women." J Clin Endocrinol Metab. 2020 Jul 1;105(7):2456–63. https://doi.org/10.1210/clinem/dgaa232 ; PMID: 32364602; PMCID: PMC7448297 , Jul-2020
Articles in Peer-reviewed Journals Grant LK, Gooley JJ, St Hilaire MA, Joffe H, Brainard GC, Van Reen E, Rüger M, Rajaratnam SMW, Lockley SW, Czeisler CA, Rahman SA. "A pilot study of light exposure as a countermeasure for menstrual phase-dependent neurobehavioral performance impairment in women." Sleep Health. 2024 Feb;10(1S):S34-S40. https://doi.org/10.1016/j.sleh.2023.08.012 ; PubMed PMID: 37748973; PubMed Central PMCID: PMC10959759 , Feb-2024
Articles in Peer-reviewed Journals Chang AM, Anderson C, Cain SW, Reichenberger DA, Ronda JM, Lockley SW, Czeisler CA. "Entrainment to gradual vs. immediate 8-hour phase advance shifts with and without short-wavelength enriched polychromatic green light." Sleep Health. 2024 Feb;10(1S):S67-S75. https://doi.org/10.1016/j.sleh.2023.09.007 ; PubMed PMID: 37989626 , Feb-2024
Awards Chang AM. (Anne-Marie Chang) "BWH Faculty Career Development Award, Eleanor and Miles Shore Harvard Scholars in Medicine, July 2012." Jul-2012
Awards Czeisler CA. "23rd Annual Catherine N. Straton Aging Successfully Lecture, Massachusetts Institute of Technology, May 2010." May-2010
Awards Czeisler CA. "Election as Full Member, International Academy of Astronautics, October 2010." Oct-2010
Awards Czeisler CA. "Election as Member, Institute of Medicine of the National Academies, October 2010." Oct-2010
Awards Czeisler CA. "Keynote Speaker, Harvard School of Public Health Symposium, September 2012." Sep-2012
Awards Czeisler CA. "Keynote Speaker, Medical Scientist Training Program, Duke University Medical School, April 2010." Apr-2010
Awards Czeisler CA. "Keynote Speaker, North East Sleep Society Annual Meeting, April 2011." Apr-2011
Awards Czeisler CA. "Keynote Speaker, World Association of Sleep Medicine, September 2011." Sep-2011
Project Title:  Evaluation of Photic Countermeasures for Circadian Entrainment of Neurobehavioral Performance and Sleep-Wake Regulation Before and During Spaceflight Reduce
Fiscal Year: FY 2011 
Division: Human Research 
Research Discipline/Element:
HRP BHP:Behavioral Health & Performance (archival in 2017)
Start Date: 05/01/2008  
End Date: 04/30/2012  
Task Last Updated: 05/04/2011 
Download Task Book report in PDF pdf
Principal Investigator/Affiliation:   Czeisler, Charles A. M.D., Ph.D. / Brigham and Women's Hospital/Harvard Medical Center 
Address:  Division of Sleep Medicine 
221 Longwood Ave., Ste. 438 
Boston , MA 02115-5804 
Email: caczeisler@rics.bwh.harvard.edu 
Phone: 617-732-4013  
Congressional District:
Web:  
Organization Type: UNIVERSITY 
Organization Name: Brigham and Women's Hospital/Harvard Medical Center 
Joint Agency:  
Comments:  
Co-Investigator(s)
Affiliation: 
Barger, Laura  Brigham and Women's Hospital 
Aeschbach, Daniel  Brigham and Women's Hospital 
Project Information: Grant/Contract No. NCC 9-58-HFP01601 
Responsible Center: NSBRI 
Grant Monitor:  
Center Contact:   
Unique ID: 7045 
Solicitation / Funding Source: 2007 Crew Health NNJ07ZSA002N 
Grant/Contract No.: NCC 9-58-HFP01601 
Project Type: Ground 
Flight Program:  
TechPort: Yes 
No. of Post Docs:
No. of PhD Candidates:
No. of Master's Candidates:
No. of Bachelor's Candidates:
No. of PhD Degrees:
No. of Master's Degrees:
No. of Bachelor's Degrees:
Human Research Program Elements: (1) BHP:Behavioral Health & Performance (archival in 2017)
Human Research Program Risks: None
Human Research Program Gaps: None
Task Description: To synchronize astronauts' circadian sleep-wake schedules to variable launch times, timed exposure to bright light and darkness in the crew quarters during the week-long pre-launch quarantine period has been used since 1990. Although successful at circadian entrainment, bright light protocols are complex to administer and astronauts' compliance is compromised because bright light glare compromises screen visibility, and increases frequency of headaches, irritability and nausea. Moreover, bright light remains unavailable as an in-flight countermeasure, requiring astronauts to rely upon hypnotics or wake-promoting therapeutics to provide symptomatic relief. Recent advances reveal that the human circadian pacemaker is most sensitive to shorter wavelength light for both phase shifting and direct enhancement of alertness and performance. We therefore propose to test the efficacy of exposure to short wavelength green light at a standard intensity for pre-launch and in-flight phase shifting.

To this end, we propose to test the circadian phase-shifting efficacy of exposure to short wavelength light throughout scheduled wake times on a protocol designed to simulate the schedule of crew members during the pre-launch quarantine period on a mission that requires an 8h phase advance of the sleep-wake schedule. Our goal is to demonstrate that exposure to ambient short wavelength fluorescent light will synchronize human circadian rhythms to a shifted sleep/wake schedule within 4-5 days, enhancing alertness and performance during the biological night.

During this proposed simulation sleep-wake schedules will be advanced by 8h using 3 different protocol designs: 1) a "slam" shift in which the sleep episode is abruptly advanced by 8h and then maintained for 4 days, 2) a gradual shift in which the sleep episode is advanced by 1.6h each day for 5 days until an 8h advance is achieved, and 3) a "slam shift with naps in which the extended wake period prior to the 8h advance of the sleep period includes 2 short nap opportunities. Given the prolonged extended wake period on the second day of the slam shift schedule the new schedule involves the opportunity to obtain two short naps: one for 2h in the afternoon circadian dip, and the second for 4h at the circadian nadir during the night. A total of 44 subjects will be studied in the project. They will be randomized to 1 of 5 protocol conditions which differ by light and by shift. The 5 conditions are 1) white light slam shift, 2) green light slam shift, 3) combined white + green light slam shift with naps, 4) white light gradual shift, and 5) green light gradual shift.

Our specific aims are to test the hypotheses that:

1. exposure to ambient polychromatic green light from will be more effective than exposure to an equal illuminance of polychromatic white in shifting circadian rhythms, as measured by dim-light melatonin onset (DLMO), in response to both a gradual 8h advance and to an abrupt shift of their sleep-wake schedule.

2. alertness and neurobehavioral performance in dim light on a constant routine during times at which crew members should be awake on the simulated mission will be significantly greater following 4-5 days of exposure to ambient polychromatic green light vs. ambient white light of equal illuminance, due to more effective circadian entrainment.

3. alertness and neurobehavioral performance will be significantly better on the first night of exposure to ambient polychromatic short wavelength light vs. ambient white light of equal illuminance, prior to the induced circadian phase shifts, due to the immediate alerting effects of exposure to ambient polychromatic short wavelength light.

4. sleep efficiency and total sleep time will be significantly increased and latency to persistent sleep and wake time after sleep onset will be significantly decreased during the sleep episode following 4-5 days of exposure to ambient polychromatic green light vs. ambient white light of equal illuminance, due to more effective circadian entrainment.

We predict that exposure to polychromatic green light throughout the day will rapidly entrain the circadian melatonin rhythm to the shifted sleep-wake schedule. We also predict that green light combined with brighter white to prevent the altered color-perception from the green light alone will enable implementation of this new technology to ensure circadian synchronization both during the pre-flight quarantine period and while aboard NASA flight vehicles. We predict that our new schedule with naps will reduce the excessive daytime sleepiness and other adverse effects often experienced with the slam shift due to prolonged wakefulness.

To date, 37 subjects have completed the 8-day protocol. Four subjects completed the white light slam shift condition in order for us to determine the best level of illuminance (90 lux) to be used for both the white and polychromatic green light. To date, 10 subjects have completed the gradual shift protocol, in either white (n=5) or green light (n=5), 21 subjects have completed the slam shift protocol, in either white (n=10) or green light (n=11), and 6 subjects have completed the combined slam shift with naps protocol. We have completed the third year ahead of schedule for enrollment (11 subjects/year), and anticipate completing the study well in advance of the end of the project period. Melatonin samples, alertness and performance testing data, and sleep recording data were collected in these studies and are currently being analyzed to address our specific aims. As per a supplemental grant (HPF00003), we implemented novel infra-red technologies into this protocol, and collected data on eye movements in n=30 subjects during periods of extended wake. New eye tracking technologies have also been implemented into the protocol, in order to examine causes of neurobehavioral deficits during periods of extended wake.

Research Impact/Earth Benefits: We will be implementing and testing a new polychromatic fluorescent lamp with a peak spectral sensitivity of ~500nm. This is near the peak sensitivity of the human circadian system, and thus should be the most efficacious polychromatic lamp for shifting the timing of the human biological clock. In addition to benefits for NASA flight personnel, this technology will also have application to shiftworkers, to jet travelers, and to any personnel who need to shift the timing of their biological rhythms.

Task Progress & Bibliography Information FY2011 
Task Progress: In the last year, we continued with our proposed study. We remained consistent with our target enrollment, studying 37 subjects in the laboratory in each of the five conditions: 10 subjects completed the gradual shift protocol, in either polychromatic white (n=5) or shorter-wavelength light (n=5), and 21 subjects completed the slam shift protocol, in either polychromatic white light (n=10) or shorter-wavelength light (n=11) and 6 subjects completed the combined slam shift with naps protocol. Melatonin samples, alertness and performance testing data, and sleep recording data were collected in these studies and are being analyzed to address our specific aims. As per a supplemental grant (HPF00003), we implemented novel infra-red technologies into this protocol, and collected data on eye movements in n=30 subjects during periods of extended wake.

Bibliography: Description: (Last Updated: 11/17/2025) 

Show Cumulative Bibliography
 
Awards Czeisler CA. "Charles A. Czeisler: Harriet Hardy Award, New England College of Occupational and Environmental Medicine (NECOEM), January 2010." Jan-2010
Awards Czeisler CA. "Charles A. Czeisler: Mark O. Hatfield Public Policy Award, American Academy of Sleep Medicine, June 2010." Jun-2010
Awards Czeisler CA. "Charles A. Czeisler: Mary A. Carskadon Outstanding Educator Award, Sleep Research Society, January 2010." Jan-2010
Project Title:  Evaluation of Photic Countermeasures for Circadian Entrainment of Neurobehavioral Performance and Sleep-Wake Regulation Before and During Spaceflight Reduce
Fiscal Year: FY 2010 
Division: Human Research 
Research Discipline/Element:
HRP BHP:Behavioral Health & Performance (archival in 2017)
Start Date: 05/01/2008  
End Date: 04/30/2012  
Task Last Updated: 05/21/2010 
Download Task Book report in PDF pdf
Principal Investigator/Affiliation:   Czeisler, Charles A. M.D., Ph.D. / Brigham and Women's Hospital/Harvard Medical Center 
Address:  Division of Sleep Medicine 
221 Longwood Ave., Ste. 438 
Boston , MA 02115-5804 
Email: caczeisler@rics.bwh.harvard.edu 
Phone: 617-732-4013  
Congressional District:
Web:  
Organization Type: UNIVERSITY 
Organization Name: Brigham and Women's Hospital/Harvard Medical Center 
Joint Agency:  
Comments:  
Co-Investigator(s)
Affiliation: 
Barger, Laura  Brigham and Women's Hospital 
Aeschbach, Daniel  Brigham and Women's Hospital 
Project Information: Grant/Contract No. NCC 9-58-HFP01601 
Responsible Center: NSBRI 
Grant Monitor:  
Center Contact:   
Unique ID: 7045 
Solicitation / Funding Source: 2007 Crew Health NNJ07ZSA002N 
Grant/Contract No.: NCC 9-58-HFP01601 
Project Type: Ground 
Flight Program:  
TechPort: Yes 
No. of Post Docs:
No. of PhD Candidates:
No. of Master's Candidates:
No. of Bachelor's Candidates:
No. of PhD Degrees:
No. of Master's Degrees:
No. of Bachelor's Degrees:
Human Research Program Elements: (1) BHP:Behavioral Health & Performance (archival in 2017)
Human Research Program Risks: None
Human Research Program Gaps: None
Task Description: To synchronize astronauts' circadian sleep-wake schedules to variable launch times, timed exposure to bright light and darkness in the crew quarters during the week-long pre-launch quarantine period has been used since 1990. Although successful at circadian entrainment, bright light protocols are complex to administer and astronauts' compliance is compromised because bright light glare compromises computer/television screen visibility, and increased frequency of headaches, irritability and nausea. Moreover, bright light remains unavailable as an in-flight countermeasure, requiring astronauts to rely upon hypnotics or wake-promoting therapeutics to provide symptomatic relief. Recent advances reveal that the human circadian pacemaker is most sensitive to shorter wavelength light for both phase shifting and direct enhancement of alertness and performance. We found that short-wavelength light (~460nm-512nm) in the blue/green range facilitates circadian phase shifting. We therefore propose to test the efficacy of exposure to short wavelength green light at a standard intensity for pre-launch and in-flight phase shifting.

To this end, we propose to test the circadian phase-shifting efficacy of exposure to short wavelength light throughout scheduled wake times on a protocol designed to simulate the schedule of crew members during the pre-launch quarantine period on a mission that requires an 8-hour phase advance of the sleep-wake schedule. Our goal is to demonstrate that exposure to ambient short wavelength fluorescent light will synchronize human circadian rhythms to a shifted sleep/wake schedule within 4-5 days, enhancing alertness and performance during the biological night.

During this proposed 8-day ground-based simulation, participants' sleep-wake schedules will be advanced by 8 hours. This advance shift will be done in 2 different protocol designs: 1) a "slam" shift in which the sleep episode is abruptly advanced by 8 hours and then maintained at this advanced time for 4 days, and 2) a gradual shift in which the sleep episode is advanced by 1.6 hours each day for 5 days until an 8 hour advance is achieved. A total of 44 subjects will be randomized to 1 of 4 protocol conditions which differ by light (ordinary indoor white light (~90 lux) or 90 lux polychromatic green light) and by shift (slam or gradual) resulting in 11 subjects/group. The 4 conditions are 1) white light slam shift, 2) green light slam shift, 3) white light gradual shift, and 4) green light gradual shift.

Our specific aims are to test the hypothesis that:

1. Exposure to ambient polychromatic short wavelength light from fluorescent lamps will be more effective than exposure to an equal illuminance of ambient polychromatic white light from standard fluorescent lamps in shifting the circadian rhythms of test subjects, as measured by dim-light melatonin onset (DLMO), in response to both a gradual 8-hour advance and to an abrupt shift of their sleep-wake schedule.

2. Alertness and neurobehavioral performance in dim light on a constant routine during times at which crew members should be awake on the simulated mission will be significantly greater following 4-5 days of exposure to ambient polychromatic green light vs. ambient white light of equal illuminance, due to more effective circadian entrainment.

3. Alertness and neurobehavioral performance will be significantly better on the first night of exposure to ambient polychromatic short wavelength light vs. ambient white light of equal illuminance, prior to the induced circadian phase shifts, due to the immediate alerting effects of exposure to ambient polychromatic short wavelength light.

4. Sleep efficiency and total sleep time will be significantly increased and latency to persistent sleep and wake time after sleep onset will be significantly decreased during the sleep episode following 4-5 days of exposure to ambient polychromatic green light vs. ambient white light of equal illuminance, due to more effective circadian entrainment.

We predict that, in contrast to white light, simple exposure to polychromatic green light throughout the day will rapidly (within five days) entrain the circadian melatonin rhythm to the shifted sleep-wake schedule, without the need for bright light exposure-rendering obsolete the crew quarters' bright light facility and enabling implementation of this new technology to ensure circadian synchronization both during the pre-flight quarantine period and while aboard NASA flight vehicles.

To date, 22 subjects have completed the 8-day protocol. Four subjects completed the white light slam shift condition in order for us to determine the best level of illuminance to be used for both the white and polychromatic green light. Melatonin samples, alertness and performance testing data, and sleep recording data were collected in these studies and are currently being analyzed to address our specific aims. Based on the melatonin results from the first 4 subjects, we proceeded to use a 90 lux level of illuminance, which is equivalent to that of ordinary indoor room light. We began randomizing enrolled subjects after completing the initial 4 subjects, with a further 18 subjects completing the protocol: 10 subjects have completed the gradual shift protocol, in either polychromatic white (n=5) or shorter-wavelength light (n=5), and 8 subjects have completed the slam shift protocol, in either polychromatic white light (n=3) or shorter-wavelength light (n=5).

As per the supplemental grant (HPF00003), we implemented novel infra-red technologies into this protocol. Eye movement data has been collected (n=15) during periods of extended wake, which will allow us to examine causes of neurobehavioral deficits during periods of extended wake.

We have completed the second year on target for enrollment (11 subjects/year), and anticipate remaining on target by the end of year 3.

Research Impact/Earth Benefits: We will be implementing and testing a new polychromatic fluorescent lamp with a peak spectral sensitivity of ~500nm. This is near the peak sensitivity of the human circadian system, and thus should be the most efficacious polychromatic lamp for shifting the timing of the human biological clock. In addition to benefits for NASA flight personnel, this technology will also have application to shiftworkers, to jet travelers, and to any personnel who need to shift the timing of their biological rhythms.

Task Progress & Bibliography Information FY2010 
Task Progress: In the last year, we continued with our research study. We remained consistent with our target enrollment, studying a total of 22 subjects in the laboratory randomly assigned to one of each of the four conditions: 10 subjects completed the gradual shift protocol, in either polychromatic white (n=5) or shorter-wavelength light (n=5), and 12 subjects completed the slam shift protocol, in either polychromatic white light (n=7) or shorter-wavelength light (n=5). Melatonin samples, alertness and performance testing data, and sleep recording data were collected in these studies and are being analyzed to address our specific aims. As per a supplemental grant (HPF00003), we implemented novel infra-red technologies into this protocol, and collected data on eye movements in n=15 subjects during periods of extended wake.

Bibliography: Description: (Last Updated: 11/17/2025) 

Show Cumulative Bibliography
 
Abstracts for Journals and Proceedings Anderson C, Chang AM, Ronda JM, Czeisler CA. "Real-time drowsiness as determined by infra-red reflectance oculography is commensurate with gold standard laboratory measures: a validation study." 24th Annual Meeting of the Associated Professional Sleep Societies, LLC, San Antonio, Texas, June 5-9, 2010.

24th Annual Meeting of the Associated Professional Sleep Societies, LLC, Abstract Book, June 2010. , Jun-2010

Project Title:  Evaluation of Photic Countermeasures for Circadian Entrainment of Neurobehavioral Performance and Sleep-Wake Regulation Before and During Spaceflight Reduce
Fiscal Year: FY 2009 
Division: Human Research 
Research Discipline/Element:
HRP BHP:Behavioral Health & Performance (archival in 2017)
Start Date: 05/01/2008  
End Date: 04/30/2012  
Task Last Updated: 05/08/2009 
Download Task Book report in PDF pdf
Principal Investigator/Affiliation:   Czeisler, Charles A. M.D., Ph.D. / Brigham and Women's Hospital/Harvard Medical Center 
Address:  Division of Sleep Medicine 
221 Longwood Ave., Ste. 438 
Boston , MA 02115-5804 
Email: caczeisler@rics.bwh.harvard.edu 
Phone: 617-732-4013  
Congressional District:
Web:  
Organization Type: UNIVERSITY 
Organization Name: Brigham and Women's Hospital/Harvard Medical Center 
Joint Agency:  
Comments:  
Co-Investigator(s)
Affiliation: 
Barger, Laura  Brigham and Women's Hospital 
Aeschbach, Daniel  Brigham and Women's Hospital 
Project Information: Grant/Contract No. NCC 9-58-HFP01601 
Responsible Center: NSBRI 
Grant Monitor:  
Center Contact:   
Unique ID: 7045 
Solicitation / Funding Source: 2007 Crew Health NNJ07ZSA002N 
Grant/Contract No.: NCC 9-58-HFP01601 
Project Type: Ground 
Flight Program:  
TechPort: Yes 
No. of Post Docs:
No. of PhD Candidates:
No. of Master's Candidates:
No. of Bachelor's Candidates:
No. of PhD Degrees:
No. of Master's Degrees:
No. of Bachelor's Degrees:
Human Research Program Elements: (1) BHP:Behavioral Health & Performance (archival in 2017)
Human Research Program Risks: None
Human Research Program Gaps: None
Task Description: To synchronize astronauts' circadian sleep-wake schedules to variable launch times, timed exposure to bright light and darkness in the crew quarters during the week-long pre-launch quarantine period has been used since 1990. Although successful at circadian entrainment, bright light protocols are complex to administer and astronauts' compliance is compromised because bright light glare compromises computer/television screen visibility, and increases frequency of headaches, irritability and nausea. Moreover, bright light remains unavailable as an in-flight countermeasure, requiring astronauts to rely upon hypnotics or wake-promoting therapeutics to provide symptomatic relief. Recent advances reveal that the human circadian pacemaker is most sensitive to shorter wavelength light for both phase shifting and direct enhancement of alertness and performance. We found that short-wavelength light (~460nm-512nm) in the blue/green range facilitates circadian phase shifting. We therefore propose to test the efficacy of exposure to short wavelength green light at a standard intensity for pre-launch and in-flight phase shifting.

To this end, we propose to test the circadian phase-shifting efficacy of exposure to short wavelength light throughout scheduled wake times on a protocol designed to simulate the schedule of crew members during the pre-launch quarantine period on a mission that requires an 8-hour phase advance of the sleep-wake schedule. Our goal is to demonstrate that exposure to ambient short wavelength fluorescent light will synchronize human circadian rhythms to a shifted sleep/wake schedule within 4-5 days, enhancing alertness and performance during the biological night.

During this proposed 8-day ground-based simulation, participants' sleep-wake schedules will be advanced by 8 hours. This advance shift will be done in 2 different protocol designs: 1) a "slam" shift in which the sleep episode is abruptly advanced by 8 hours and then maintained at this advanced time for 4 days, and 2) a gradual shift in which the sleep episode is advanced by 1.6 hours each day for 5 days until an 8 hour advance is achieved. A total of 44 subjects will be studied in the project. They will be randomized to 1 of 4 protocol conditions which differ by light (ordinary indoor white light (~90 lux) or 90 lux polychromatic green light) and by shift (slam or gradual) so that there will be 11 subjects/group. The 4 conditions are 1) white light slam shift, 2) green light slam shift, 3) white light gradual shift, and 4) green light gradual shift.

Our specific aims are to:

1. Test the hypothesis that exposure to ambient polychromatic short wavelength light from fluorescent lamps will be more effective than exposure to an equal illuminance of ambient polychromatic white light from standard fluorescent lamps in shifting the circadian rhythms of test subjects, as measured by dim-light melatonin onset (DLMO), in response to both a gradual 8-hour advance and to an abrupt shift of their sleep-wake schedule.

2. Test the hypothesis that alertness and neurobehavioral performance in dim light on a constant routine during times at which crew members should be awake on the simulated mission will be significantly greater following 4-5 days of exposure to ambient polychromatic green light vs. ambient white light of equal illuminance, due to more effective circadian entrainment.

3. Test the hypothesis that alertness and neurobehavioral performance will be significantly better on the first night of exposure to ambient polychromatic short wavelength light vs. ambient white light of equal illuminance, prior to the induced circadian phase shifts, due to the immediate alerting effects of exposure to ambient polychromatic short wavelength light.

4. Test the hypothesis that sleep efficiency and total sleep time will be significantly increased and latency to persistent sleep and wake time after sleep onset will be significantly decreased during the sleep episode following 4-5 days of exposure to ambient polychromatic green light vs. ambient white light of equal illuminance, due to more effective circadian entrainment.

We predict that, in contrast to white light, simple exposure to polychromatic green light throughout the day will rapidly (within five days) entrain the circadian melatonin rhythm to the shifted sleep-wake schedule, without the need for bright light exposure-rendering obsolete the crew quarters' bright light facility and enabling implementation of this new technology to ensure circadian synchronization both during the pre-flight quarantine period and while aboard NASA flight vehicles.

To date, 5 subjects have completed the 8-day protocol. Four subjects completed the white light slam shift condition in order for us to determine the best level of illuminance to be used for both the white and polychromatic green light. Melatonin samples, alertness and performance testing data, and sleep recording data were collected in these studies and are being analyzed to address our specific aims. Based on the melatonin results from these first 4 subjects, we have decided to use a 90 lux level of illuminance, which is equivalent to that of ordinary indoor room light. The polychromatic fluorescent lamps have been installed in our laboratory and calibrated so as to achieve 90 lux. We began randomizing enrolled subjects after completing the initial 4 subjects and 1 additional subject has completed the white light gradual shift condition, with 3 additional subjects scheduled to complete the study in April 2009.

We are continuing to enroll subjects and expect to be on target with enrollment (11 subjects/year) by the end of the first year of the project. In the coming year we anticipate being on or ahead of pace with at least 22 subjects completed by the end of year 2.

Research Impact/Earth Benefits: We will be implementing and testing a new polychromatic fluorescent lamp with a peak spectral sensitivity of ~500nm. This is near the peak sensitivity of the human circadian system, and thus should be the most efficacious polychromatic lamp for shifting the timing of the human biological clock. In addition to benefits for NASA flight personnel, this technology will also have application to shiftworkers, to jet travelers, and to any personnel who need to shift the timing of their biological rhythms.

Task Progress & Bibliography Information FY2009 
Task Progress: In the last year, we implemented our proposed study. This included: designing a subject recruitment plan and implementing that plan to recruit and screen study participants; determining, based on results from our prior NSBRI-funded project as well as results from other ongoing projects in our laboratory that the peak sensitivity of the human circadian system is closer to 500nm than to 460nm; based on the new information about the peak sensitivity of the human circadian system, determining that the most efficacious specialized light source should have a peak near 500nm (as opposed to ~470nm as the lamps produced by Philips Lighting, Eindhoven, Netherlands, as originally proposed), and therefore identifying such a new specialized light source for our studies; retrofitting our laboratory with specialized lamps (manufactured by Sunnex Biotechnologies, Winnipeg, MB, Canada) with a peak sensitivity near 500nm; conducting calibrations of our laboratory to ensure the control lighting and the test lighting are applied similarly; and conducting preliminary tests to determine the level of lighting to be tested. To date, 5 subjects have completed the 8-day protocol. Melatonin samples, alertness and performance testing data, and sleep recording data were collected in these studies and are being analyzed to address our specific aims. We began randomizing enrolled subjects after completing the initial 4 subjects and 1 additional subject has completed the white light gradual shift condition.

Bibliography: Description: (Last Updated: 11/17/2025) 

Show Cumulative Bibliography
 
Abstracts for Journals and Proceedings Burke TM, Scheer FA JL, Ronda JM, Czeisler CA, Wright KP. "Contribution of homeostatic, circadian and sleep inertia processes on higher order cognitive functions using a forced desynchrony protocol." SLEEP 2009 23rd Annual Meeting of the Associated Professional Sleep Societies, LLC, Seattle, WA, June 6-11, 2009.

SLEEP 2009 23rd Annual Meeting of the Associated Professional Sleep Societies, LLC, 2009. Abstract Book. , Jun-2009

Abstracts for Journals and Proceedings Santhi N, Duffy JF, Czeisler CA. "Attentional failures are more pronounced in the latter half of a wake episode following an inversion of the sleep-wake schedule." SLEEP 2009 23rd Annual Meeting of the Associated Professional Sleep Societies, LLC, Seattle, WA, June 6-11, 2009.

SLEEP 2009 23rd Annual Meeting of the Associated Professional Sleep Societies, LLC, 2009. Abstract Book. , Jun-2009

Awards Czeisler CA. "Distinguished Scientist Award, Sleep Research Society, June 2008." Jun-2008
Awards Czeisler CA. "Lifetime Achievement Award, National Sleep Foundation, March 2008." Mar-2008
Awards Czeisler CA. "Lord Adrian Medal, Royal Society of Medicine, London, April 2008." Apr-2008
Project Title:  Evaluation of Photic Countermeasures for Circadian Entrainment of Neurobehavioral Performance and Sleep-Wake Regulation Before and During Spaceflight Reduce
Fiscal Year: FY 2008 
Division: Human Research 
Research Discipline/Element:
HRP BHP:Behavioral Health & Performance (archival in 2017)
Start Date: 05/01/2008  
End Date: 04/30/2012  
Task Last Updated: 05/30/2008 
Download Task Book report in PDF pdf
Principal Investigator/Affiliation:   Czeisler, Charles A. M.D., Ph.D. / Brigham and Women's Hospital/Harvard Medical Center 
Address:  Division of Sleep Medicine 
221 Longwood Ave., Ste. 438 
Boston , MA 02115-5804 
Email: caczeisler@rics.bwh.harvard.edu 
Phone: 617-732-4013  
Congressional District:
Web:  
Organization Type: UNIVERSITY 
Organization Name: Brigham and Women's Hospital/Harvard Medical Center 
Joint Agency:  
Comments:  
Co-Investigator(s)
Affiliation: 
Aeschbach, Daniel  Brigham & Women's Hospital 
Barger, Laura  Brigham & Women's Hospital 
Project Information: Grant/Contract No. NCC 9-58-HFP01601 
Responsible Center: NSBRI 
Grant Monitor:  
Center Contact:   
Unique ID: 7045 
Solicitation / Funding Source: 2007 Crew Health NNJ07ZSA002N 
Grant/Contract No.: NCC 9-58-HFP01601 
Project Type: Ground 
Flight Program:  
TechPort: Yes 
No. of Post Docs:  
No. of PhD Candidates:  
No. of Master's Candidates:  
No. of Bachelor's Candidates:  
No. of PhD Degrees:  
No. of Master's Degrees:  
No. of Bachelor's Degrees:  
Human Research Program Elements: (1) BHP:Behavioral Health & Performance (archival in 2017)
Human Research Program Risks: None
Human Research Program Gaps: None
Task Description: To synchronize astronauts circadian sleep-wake schedules to variable launch times, timed exposure to bright light and darkness in the astronaut crew quarters during the week-long pre-launch quarantine period has been used since 1990. Although successful at circadian entrainment, bright light protocols are complex to administer and astronauts compliance is compromised because bright light glare compromises computer/television screen visibility, and increases frequency of headaches, irritability and nausea. Moreover, bright light remains unavailable as an inflight countermeasure, requiring astronauts to rely upon hypnotics or wake-promoting therapeutics to provide symptomatic relief.

Recent advances over the past six years have revealed that the human circadian pacemaker is most sensitive to shorter wavelength (blue) light for both phase shifting and direct enhancement of alertness and performance. While the monochromatic blue (~460 nm) light used for research is not a practical spaceflight countermeasure because of its adverse effects on color vision, we have shown blue-enriched white light to facilitate circadian phase shifts.

This project will test the efficacy of exposure to blue-enriched light at a standard intensity for pre-launch and inflight phase shifting. During this ground-based simulation of the pre-launch quarantine period, participants sleep-wake schedules will be shifted (advanced) by eight hours. Groups (n=16 subjects/light condition) will be randomized to four-day exposures to either: ordinary indoor white light (~50 lux) or 50 lux polychromatic blue-enriched light.

We predict that, in contrast to white light, simple exposure to blue-enriched light throughout the day will rapidly (within four days) entrain the circadian melatonin rhythm to the shifted sleep-wake schedule without the need for bright light exposure rendering obsolete the crew quarters bright-light facility and enabling implementation of this new technology to ensure circadian synchronization both during the preflight quarantine period and while aboard NASA flight vehicles.

Research Impact/Earth Benefits:

Task Progress & Bibliography Information FY2008 
Task Progress: New project for FY2008.

Bibliography: Description: (Last Updated: 11/17/2025) 

Show Cumulative Bibliography
 
 None in FY 2008