- Short Report
- Open Access
Implications of controlled short-wavelength light exposure for sleep in older adults
© Figueiro et al; licensee BioMed Central Ltd. 2011
- Received: 6 April 2011
- Accepted: 8 September 2011
- Published: 8 September 2011
Environmental and physiological conditions make older adults more likely to lose synchronization to their local time and experience sleep disturbances. A regular, 24-hour light/dark cycle promotes synchronization. It is now well established that the circadian system is maximally sensitive to short-wavelength (blue) light. The purpose of the present study was to measure dose effectiveness (amounts and durations) of short-wavelength (blue) light for stimulating the circadian systems of older adults. We investigated the impact of six corneal irradiances (0.7 to 72 μW/cm2) of 470-nm light on nocturnal melatonin production. Nine participants, each over 50 years of age completed a within-subjects study. Each week, participants were exposed to one of the six irradiances of 470-nm light for 90 minutes.
A two-factor (6 corneal irradiances × 10 exposure durations), within-subjects analysis of variance (ANOVA) was conducted using the melatonin suppression levels. The ANOVA revealed a significant main effect of corneal irradiance (F5, 30 = 9.131, p < 0.0001), a significant main effect of exposure duration (F9, 54 = 5.731, p < 0.0001), and a significant interaction between these two variables (F45,270 = 1.927, p < 0.001). Post hoc t-tests revealed that corneal irradiances as low as 2 μW/cm2 reliably suppressed melatonin after 90-minute exposure whereas 0.7 μW/cm2 did not.
Sleep disorders are common and a serious problem for millions of older adults. The present results showed that comfortable, precise and effective doses of light can be prescribed to older adults to reliably stimulate the circadian system that presumably would promote entrainment and, thus, regular sleep. Field studies on the impact of short-wavelength-light doses on sleep efficiency in older adults should be performed.
- Exposure Duration
- Pupil Diameter
- Circadian System
- Light Dose
A large and growing body of research shows that a regular, 24-hour light/dark cycle synchronizes circadian rhythms in all species, including humans, to local time on earth. Light levels required to activate the circadian system are higher than those required for vision . Since older adults are less active and tend to stay indoors more often where light levels tend to be low, they may not be exposed to lighting that sufficiently stimulates their circadian system . Moreover, these same older adults commonly have less light reaching their retina due to natural age-related reductions in pupil size (senile miosis) and in crystalline lens transmission . Together, these environmental and physiological conditions make older adults more likely to lose entrainment to their local time and, as a result, more likely to experience sleep disturbances [2, 4, 5].
Timed light treatments have been shown to improve circadian entrainment in older persons, including those with Alzheimer's disease (AD), a population that is perhaps most susceptible to circadian disruption through light restriction . Clinical research has shown, for example, that exposing persons with AD to light levels higher than what they would normally experience in their homes or in institutions during the day and darkness at night can consolidate their rest/activity patterns [7, 8]. Morning and evening bright light exposures (> 2,500 lux at the cornea) have been shown to improve nighttime sleep, increase daytime wakefulness, reduce evening agitation behavior, and consolidate rest/activity patterns of persons with AD [8–11]. Riemersma-van der Lek and colleagues demonstrated that all-day exposure to high levels of a white light (i.e., at least 1000 lux at the eye of a 4100 K light source) improved sleep efficiency and cognition in patients with AD as well as reduced symptoms of depression . Light applied in the evening has also been shown to be effective in phase delaying the circadian system of older people without dementia, allowing them to fall asleep later and wake up later .
Although bright light interventions appear to be effective for promoting circadian entrainment and improving sleep efficiency, they can be expensive, time consuming for caregivers, and uncomfortable for older adults, who show symptoms of photophobia. In fact, there is evidence that light treatment may not always result in better sleep in older adults. Light treatment alone (1 hour of 2,500 lux at the angle of gaze) did not improve nighttime sleep, daytime wake and rest activity in AD patients [14, 15]. These negative results may reflect problems with compliance, so there is a need to develop more practical and, thus, more effective methods for light delivery.
Treatment efficacy (i.e., effectiveness per electrical watt) is also important to consider for practical applications. One simple method for improving treatment efficacy is placing the light source closer to the eyes. The irradiance at the cornea falls off with the square of the distance from the source, so small reductions in this distance have disproportionately large increases in light exposure to the retina. Tuning the light spectrum for maximum effect also increases treatment efficacy. Research has demonstrated that the spectral sensitivity of the circadian system differs from the spectral sensitivity of the achromatic visual channel, which is used for such visual activities as reading. Short-wavelength (blue) light between approximately 440 nm and 470 nm is maximally effective at stimulating the human circadian system, as measured through acute melatonin suppression and phase shifting of the melatonin rhythm [16–18].
One way to provide older adults with inexpensive, low-powered light sources that provide sufficient levels of circadian-effective light would be to mount short-wavelength light-emitting diodes (LEDs) on spectacle frames. With a thoughtful design, the intensity distribution of the circadian-effective light sources should not interfere with the performance of visual tasks. Some engineering sophistication is also needed to precisely control the timing and duration of the light dose. Temporally controlled 470-nm (blue) LEDs mounted on spectacle frames would be inexpensive, require little, if any, maintenance, and would be comfortable and safe for users as long as the dose was properly prescribed. A prototype of the device was developed and its effectiveness at two irradiances was measured previously by Figueiro et al .
The purpose of the present study was to extend the findings from Figueiro et al  to more precisely measure dose effectiveness (amounts and durations) of short-wavelength (blue) light for stimulating the circadian systems of older adults. A self-powered, blue-light goggle system had been developed for the previous study and was used again here to deliver the light doses. Nocturnal melatonin suppression was used as the measure of the threshold for light activation and of dose efficacy. In addition, these data would be expected to be used to refine the mathematical model of human circadian phototransduction  to predict circadian effectiveness for other light sources. Once the dose effectiveness for short-wavelength stimulus is known, the dose effectiveness for other narrowband sources can be estimated from the modeled spectral sensitivity function.
The prototype blue-light goggles were developed under a grant from the National Institutes on Aging to deliver circadian-effective light doses to adults 50 years of age and older. Previously, nocturnal melatonin suppression was measured at just two light doses from these blue-light goggles . The present study was designed to extend those findings by measuring the effectiveness of additional doses from these goggles for suppressing nocturnal melatonin in older adults. The Institute Review Board (IRB) of Rensselaer Polytechnic Institute approved the present experimental protocol and all subjects were asked to sign a written informed consent form.
Of the eleven subjects who completed the previous study , nine were still available for further study; therefore only data for the nine subjects who completed all experimental conditions are included here. These subjects had been previously recruited through e-mail notices, posters, and word-of-mouth. Eligibility for the study required subjects to be over the age of 50 years and to be free of any major health problems, such as cardiovascular disease, diabetes, or high blood pressure. Potential subjects were excluded if they were taking over-the-counter melatonin or prescription medication such as blood pressure medicine, antidepressants, sleep medicine, hormone replacement therapy or beta-blockers. Potential subjects who stated they had any eye disease (such as cataract, glaucoma and color blindness) were not accepted into the study. Seven of nine subjects completed the Munich ChronoType questionnaire (MCTQ) . Because the experiment would be conducted in the early part of the night, extreme late chronotypes were excluded to assure melatonin levels would be high at the time of the experiment; of the seven subjects who completed the MCTQ, all were moderate to early chronotypes with a mean ± standard deviation of 1.3 ± 1.0. All subjects contributing to the present results were between 51 and 62 years of age (mean ± standard deviation, 56.2 ± 3.9 years).
Subjects who completed the 2-night protocol reported by Figueiro et al  took part in the additional five-night protocol; the sessions took place on Friday nights (between September 2009 and April 2010) and were scheduled at least one week apart. On the weeks of the experimental sessions, subjects were instructed to go to bed between 21:00 and 23:00. On the day of the experiment, subjects were asked to refrain from caffeine and alcohol 12 hours prior to the start of the experiment and to arrive at the lab at 22:00. Upon arrival, a registered nurse inserted an indwelling catheter into an arm of each subject. At 23:00, room lights were turned off, except for two red LED traffic signal lights (λmax = 640 nm) placed on the floor, outside the subjects' field of view. These traffic signals provided indirect illumination in the space, less than 1 lux at the cornea, that was sufficient for people to safely navigate in the space without stimulating their circadian systems.
After the room lights were turned off, the subjects were seated and watched a movie that was projected on a screen about 20 feet (6 meters) away. The measured (polychromatic) illuminance at the subjects' cornea reflected from the projection screen alone ranged from 0.14 to 0.2 lux; this level is too low to stimulate the circadian system . The movie kept subjects awake, minimizing the likelihood of eye closures. Moreover, experimenters continuously monitored the subjects to ensure that they had their eyes open. Subjects were not allowed to drink or eat after 23:30.
Data collection times for the first subject in a session to provide blood and saliva samples
One saliva and three blood samples were collected from each subject at each of seven appointed times in a 90-minute session. Saliva samples were obtained using the Salivette system (ALPCO Diagnostics, Salem, NH, USA). Three, 3-ml blood samples were drawn by the nurse at each of the prescribed times; the first sample was always discarded and the second and third samples were spun in a centrifuge for 15 minutes. Frozen saliva and plasma samples were subsequently sent to an independent laboratory (Pharmasan Labs, Osceola, WI) for melatonin radioimmunoassay. The sensitivity of the saliva assay was 0.7 pg/ml and the intra- and inter-assay coefficients of variability (CVs) were 12.1% and 13.2%, respectively. The sensitivity of the plasma assay was 3.5 pg/ml and the intra- and inter-assay CVs were 8.1% and 14.8%, respectively.
Lighting conditions presented to subjects
5.5 (5.4 ± 0.51)
0.7 (0.7 ± 0.04)
0.61(0.6 ± 0.16)
473 (473 ± 0.4)
18 (18 ± 0.83)
5.3 (5.2 ± 0.52)
2.0 (2 ± 0.08)
1.2 (1.5 ± 0.37)
462 (467 ± 5.5)
18 (18 ± 0.29)
4.9 (4.8 ± 0.53)
6.1 (6 ± 0.2)
5.8 (6.8 ± 3.1)
474 (474 ± 0.3)
20 (20 ± 0.3)
4.2 (4.4 ± 0.61)
11 (11 ± 2.6)
11 (11 ± 1.6)
474 (474 ± 1.8)
20 (20 ± 0.5)
3.8 (4.1 ± 0.91)
20 (20 ± 0.4)
12 (14 ± 4.1)
462 (466 ± 5.9)
19 (19 ± 1.1)
3.8 (4.1 ± 0.87)
72 (74 ± 7.3)
66 (60 ± 17)
473 (469 ± 6.3)
20 (20 ± 1.5)
3.4 (3.4 ± 0.33)
At completion of pupil measurements (described below), room lighting was turned on and the registered nurse removed the indwelling catheter from the subjects' arms and subjects were offered a ride home.
Topbulb.com produced the blue-light goggles used to deliver the prescribed doses of light from LUXEON Rebel (LXML - PB01) LEDs. Subjects wore the goggles while they received one of seven irradiance levels at the cornea, including the dark control condition without energizing the LEDs. Table 2 shows the six average irradiance (μW/cm2) and illuminance (lux) levels, as well as the peak and full width at half maximum (FWHM) wavelengths generated by the energized goggles.
Four LEDs, two per goggle lens, with peak wavelengths ranging from 466 to 474 nm were mounted to the top inside rim of the goggles. The LEDS were located behind a translucent plastic tube to diffuse the light and to reduce point-source glare . Although the amount of light emitted by the LEDs was below levels that might be of concern for blue light hazard , diffusing the light sources further ensured safety. Heat from the LEDs was dissipated via a heat sink strip. The LEDs were connected by wire to a small control case (0.5 × 1.5 × 2.5 in. [1.3 × 3.8 × 6.4 cm]), which held a 3.0 VDC two-battery power source, and the control circuitry, including a Texas Instruments voltage regulator (TPS77018DBVR 1.8 V). The small control case also housed the LED driver (Maxim Evaluation Kit -1848 EVKIT), which was used to adjust the flux emitted by the LEDs to the prescribed light level in a session.
Prior to every session, new batteries were inserted into the small control case. While the LED driver was adjusted, light from the left and from the right goggle lens LEDs were alternately measured with a Model 2300i Action Research double monochrometer a Spectra Sense Version 4.3.0 spectral radiometer using a 5 mm diameter optical fiber ending in a lambertian diffuser as the sensor. During measurements, the sensor was placed where the subject's corneas would be while wearing the goggles. The average irradiance from the left and right lenses was used to meet the prescribed light level.
After each session, while a subject continued to wear the blue-light goggles at the session-prescribed corneal irradiance, ten digital images of one eye of each subject were acquired with a Sony video camera. To improve camera image quality, an infrared (IR) source irradiated the eye. Pupil size is unaffected by this supplemental source because the retina is insensitive to IR radiation. Subjects held a small ruler just below their eye during the image capture as a reference, linear scale to estimate pupil diameter. The captured image was printed and, using precise calipers, the experimenter measured both the size of the known ruler unit (e.g., 1 cm) and the size of the unknown pupil diameter in the image. The ratio of the measured ruler unit from the digital image to the known ruler unit was then used to scale the measured pupil diameter from the digital image to estimate the actual pupil diameter. Three images were arbitrarily selected and used to estimate the pupil diameter for a given subject. Thus, the reported median pupil diameters in Table 2 are each based upon the median of 27 pupil diameter estimates (9 subjects × 3 samples). From the median pupil diameters, pupil areas were calculated. Since there was no evidence of anisocoria with any subject, the size of both the left and right pupils should always be the same. Binocular retinal light exposures were defined as the product of the median corneal irradiance and the median pupil area in units of deka-nanowatts (μW/cm2 × mm2) or micro-lumens (lm/m2 × mm2) where corneal illuminance is considered.
Probabilities of a Type 1 error using one sample Student's t-test
Corneal irradiance (μW/cm2)
The present results investigated the impact of 90-minute exposures from six corneal irradiances (0.7 to 72 μW/cm2) of 470-nm (blue) light on acute nocturnal melatonin suppression. In general, as irradiances and duration of exposure increased, melatonin suppression increased. The present data also showed that statistically significant melatonin suppression was observed after 90-minute exposure to 2 μW/cm2, suggesting that the threshold for acute suppression by a 470-nm light is between 0.7 μW/cm2 and 2 μW/cm2 for this population.
Sleep disorders are common and a serious problem for millions of older adults [24–26]. Family members, friends, and health care workers who provide care to these individuals are also severely impacted by sleep disorders. Pharmaceuticals are commonly used to treat sleep problems with mixed success and at a fairly high cost. Light therapy to correct circadian disruption may be a practical, inexpensive, and an effective treatment alternative for older adults with sleep disorders. The present data, together with a model of human circadian phototransduction , enables researchers to make refined quantitative predictions of light doses and clinicians to more precisely prescribe light doses to treat circadian sleep disorders in older adults.
Administering light through a personal device does not require the person to be seated in front of a light box for a long period of time. Individuals can wear the device while performing routine tasks in the home. As shown here, although no formal collection protocol was used, informal discussions with subjects at the end of the experiment revealed that they could comfortably watch a movie in a darkened room while receiving their light dose. As a result of tuning the temporal-spatial-spectral-absolute characteristics of light to the human circadian system, it is possible to prescribe comfortable and effective doses of light to reliably stimulate the circadian system. This tuning reduces glare and discomfort associated with bright white light and should thereby increase light treatment compliance. Simple control technologies, yet to be developed, would ensure that the light delivery is provided at the right time and for the shortest duration to promote circadian entrainment. The personal light treatment device is inherently inexpensive to fabricate, calibrate, and obviates replacing or retrofitting existing light fixtures to deliver an effective dose of light. This is especially important for many assisted living facilities or nursing homes with low budgets.
In summary, the present study was able to quantify the efficacy of a personal light treatment device for stimulating the circadian systems of older adults without risk of retinal damage . In fact, the radiances utilized in the study were well below levels that pose a blue-light hazard risk . Although the present data were collected in the middle of the night, this device should be used to deliver light treatment during the daytime or during the early evening hours. Additional studies are recommended to investigate the ability of short-wavelength (blue) light applied during the morning or evening hours to phase shift or to entrain the circadian systems of older adults suffering from circadian sleep disorders. Additional studies are also recommended to investigate the impact of blue-light treatment for subjective daytime sleepiness and nighttime sleep quality as well as for wake and sleep electroencephalogram. Notwithstanding these important limitations of the present study, the primary envisioned benefit of a personal light treatment device is that clinicians can begin to prescribe a precise dose of short-wavelength (blue) light for older adults to reliably stimulate their circadian systems . Once a dose is determined, its brightness would be the lowest possible because the spectrum is tuned to maximum circadian effectiveness. This also has the benefit of limiting wasted heat from the LED, both improving energy efficiency and minimizing tactile discomfort. A low-brightness, battery-operated device that is safe, comfortable, and portable can provide older adults with an effective light dose while they perform their daily activities, eliminating the need to sit in front of a light box.
Two further limitations of the present study are that user acceptance was not formally evaluated and the effectiveness of blue light exposures was not tested in older adults who exhibit health problems. Although the efficacy of blue-light treatment for improving sleep efficiency in older adults, including those with AD, has been demonstrated in earlier studies [27, 28], there are no empirical data to directly support acceptance, compliance, or efficacy for treatment of sleep disorders in larger clinical trials using older adults who are not as healthy as those who participated in the present study. Further, the device used in the present study is not yet a commercial product so customer feedback in other areas, like cost, was not obtained. Still, the device seems quite promising for formal tests of user acceptance.
Acknowledgements and Funding
The studies were supported in part by the Engineering Research Centers Program of the National Science Foundation under NSF Cooperative Agreement No. EEC-0812056, in part by New York State under NYSTAR contract C090145, and in part by the National Institute on Aging at the National Institutes of Health (grant number R41 AG019693). The authors would like to acknowledge Phil Bonello of Topbulb.com for providing the goggles prototype (through the NIA grant) and A. Bierman, J. Bullough, B. Erdener, K. Kubarek, B. Plitnick, B. Wood, L. Radetsky, and D. Guyon of the Lighting Research Center for their assistance with the studies and data analyses.
- Rea MS, Figueiro MG, Bullough JD: Circadian photobiology: An emerging framework for lighting practice and research. Light Res Technol. 2002, 34: 177-190. 10.1191/1365782802lt057oa.View ArticleGoogle Scholar
- Van Someren EJ: Circadian rhythms and sleep in human aging. Chronobiol Int. 2000, 17: 233-243. 10.1081/CBI-100101046.PubMedView ArticleGoogle Scholar
- Weale R: The Senescence of Human Vision. 1992, Oxford: University PressGoogle Scholar
- Ancoli-Israel S, Kripke DF: Prevalent sleep problems in the aged. Biofeedback Self Regul. 1991, 16: 349-359. 10.1007/BF00999989.PubMedView ArticleGoogle Scholar
- Pollak CP, Perlick D: Sleep problems and institutionalization of the elderly. J Geriatr Psychiatry Neurol. 1991, 4: 204-210. 10.1177/089198879100400405.PubMedView ArticleGoogle Scholar
- Van Someren EJ, Hagebeuk E, Lijzenga C, Scheltens P, de Rooij S, Jonker C, et al: Circadian rest-activity rhythm disturbances in Alzheimer's disease. Biol Psychiatry. 1996, 40: 259-270. 10.1016/0006-3223(95)00370-3.PubMedView ArticleGoogle Scholar
- Ancoli-Israel S, Gehrman P, Martin JL, Shochat T, Marler M, Corey-Bloom J, et al: Increased light exposure consolidates sleep and strengthens circadian rhythms in severe Alzheimer's disease patients. Behav Sleep Med. 2003, 1: 22-36. 10.1207/S15402010BSM0101_4.PubMedView ArticleGoogle Scholar
- Van Someren EJ, Kessler A, Mirmirann M, Swaab D: Indirect bright light improves circadian rest-activity rhythm disturbances in demented patients. Biol Psychiatry. 1997, 41: 955-963. 10.1016/S0006-3223(97)89928-3.PubMedView ArticleGoogle Scholar
- Mishima K, Hishikawa Y, Okawa M: Randomized, dim light controlled, crossover test of morning bright light therapy for rest-activity rhythm disorders in patients with vascular dementia and dementia of Alzheimer's type. Chronobiol Int. 1998, 15: 647-654. 10.3109/07420529808993200.PubMedView ArticleGoogle Scholar
- Mishima K, Okawa M, Hishikawa Y, Hozumi S, Hori H, Takahashi K: Morning bright light therapy for sleep and behavior disorders in elderly patients with dementia. Acta Psychiatr Scand. 1994, 87: 1-7.View ArticleGoogle Scholar
- Koyama E, Matsubara H, Nakano T: Bright light treatment for sleep-wake disturbances in aged individuals with dementia. Psychiatry Clin Neurosci. 1999, 53: 227-229. 10.1046/j.1440-1819.1999.00483.x.PubMedView ArticleGoogle Scholar
- Riemersma-van der Lek RF, Swaab DF, Twisk J, Hol EM, Hoogendijk WJ, Van Someren EJ: Effect of bright light and melatonin on cognitive and noncognitive function in elderly residents of group care facilities: a randomized controlled trial. Jama. 2008, 299: 2642-2655. 10.1001/jama.299.22.2642.PubMedView ArticleGoogle Scholar
- Campbell SS, Terman M, Lewy AJ, Dijk DJ, Eastman CI, Boulos Z: Light treatment for sleep disorders: consensus report. V. Age-related disturbances. J Biol Rhythms. 1995, 10: 151-154. 10.1177/074873049501000207.PubMedView ArticleGoogle Scholar
- Dowling GA, Burr RL, Van Someren EJ, Hubbard EM, Luxenberg JS, Mastick J, et al: Melatonin and bright-light treatment for rest-activity disruption in institutionalized patients with Alzheimer's disease. J Am Geriatr Soc. 2008, 56: 239-246. 10.1111/j.1532-5415.2007.01543.x.PubMedPubMed CentralView ArticleGoogle Scholar
- Dowling GA, Hubbard EM, Mastick J, Luxenberg JS, Burr RL, Van Someren EJ: Effect of morning bright light treatment for rest-activity disruption in institutionalized patients with severe Alzheimer's disease. Int Psychogeriatr. 2005, 17: 221-236. 10.1017/S1041610205001584.PubMedPubMed CentralView ArticleGoogle Scholar
- Brainard G, Hanifin J, Greeson J, Byrne B, Glickman G, Gerner E, et al: Action spectrum for melatonin regulation in humans: Evidence for a novel circadian photoreceptor. J Neurosci. 2001, 21: 6405-6412.PubMedGoogle Scholar
- Rea MS, Figueiro MG, Bullough JD, Bierman A: A model of phototransduction by the human circadian system. Brain Res Rev. 2005, 50: 213-228. 10.1016/j.brainresrev.2005.07.002.PubMedView ArticleGoogle Scholar
- Thapan K, Arendt J, Skene DJ: An action spectrum for melatonin suppression: evidence for a novel non-rod, non-cone photoreceptor system in humans. J Physiol. 2001, 535: 261-267. 10.1111/j.1469-7793.2001.t01-1-00261.x.PubMedPubMed CentralView ArticleGoogle Scholar
- Figueiro MG, Bierman A, Bullough JD, Rea MS: A personal light-treatment device for possibly improving sleep quality in the elderly: Dynamics of nocturnal melatonin suppression at two exposure levels. Chronobiology International. 2009, 26: 726-739. 10.1080/07420520902927809.PubMedPubMed CentralView ArticleGoogle Scholar
- Roenneberg T, Wirz-Justice A, Merrow M: Life between clocks: daily temporal patterns of human chronotypes. J Biol Rhythms. 2003, 18: 80-90. 10.1177/0748730402239679.PubMedView ArticleGoogle Scholar
- Zeitzer J, Dijk D, Kronauer R, Brown E, Czeisler C: Sensitivity of the human circadian pacemaker to nocturnal light: melatonin phase resetting and suppression. J Physiol. 2000, 526 (Pt 3): 695-702.PubMedPubMed CentralView ArticleGoogle Scholar
- Luckiesh MH, Guth SK: Brightnesses in visual field at borderline between comfort and discomfort (BCD). Illuminating Engineering. 1949, 650-670. 44Google Scholar
- Bullough JD: The blue-light hazard: A review. Journal of the Illuminating Engineering Society. 2000, 29: 6-14, 141.View ArticleGoogle Scholar
- Foley DJ, Monjan AA, Brown SL, Simonsick EM, Wallace RB, et al: Sleep complaints among elderly persons: an epidemiologic study of three communities. Sleep. 1995, 18: 425-432.PubMedGoogle Scholar
- McCurry SM, Ancoli-Israel S: Sleep Dysfunction in Alzheimer's Disease and Other Dementias. Curr Treat Options Neurol. 2003, 5: 261-272. 10.1007/s11940-003-0017-9.PubMedView ArticleGoogle Scholar
- Van Someren EJ: Circadian and sleep disturbances in the elderly. Exp Gerontol. 2000, 35: 1229-1237. 10.1016/S0531-5565(00)00191-1.PubMedView ArticleGoogle Scholar
- Figueiro MG, Rea MS, LEDs: Improving the sleep quality of older adults. Proceedings of the CIE Midterm Meeting and International Lighting Congress 12-21 May, 2005. 2005, Leon, Spain. Commission Internationale de L'EclairageGoogle Scholar
- Figueiro MG, Saldo E, Rea MS, Kubarek K, Cunningham J, et al: Developing Architectural Lighting Designs to Improve Sleep in Older Adults. The Open Sleep Journal. 2008, 12: 40-51.View ArticleGoogle Scholar
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