Name: collecting sleep, circadian, fatigue, and performance data in complex operational environments
Uploaded: 2019-08-08T14:30:00
Duration: 8 min 36 s
Description: Watch this Scientific Journal Video about Collecting Sleep, Circadian, Fatigue, and Performance Data in Complex Operational Environments at JoVE.com

We thank the study participants and airline personnel for their support in data collection. We also thank the members of the Fatigue Countermeasures Laboratory at NASA Ames Research Center for their assistance with this project. This research was supported by the NASA Systemwide Safety Program.

EEFE is a consultant for Baby Sleep Science and she has received travel funding from Washington State University, the University of Chicago, the Puget Sound Pilots, the National Safety Council, and the American Academy of Sleep Medicine and Sleep Research Society. The other authors have no disclosures to report.

The methods described in this manuscript provide insight into sleep patterns, circadian phases, fatigue ratings, and performances of pilots during daytime flights including early starts, high workload mid-day flights, and late finishes. The combination of these methods demonstrated that these factors are all affected by modest changes in work start time and workload. By evaluating a systematic study schedule and integrating these measures into an easy-to-use touch-screen application, a large amount of data was collected in a challenging environment. Using this combination of methods allowed for a clearer interpretation of changes in alertness and performance during non-traditional daytime work shifts.
This design and implementation of methods measuring objective sleep, circadian, fatigue, and performance data were critical in allowing the determination of how work start-time influences pilots during daytime flights in the absence of jet lag. The protocol was designed to allow for systematic comparisons between conditions, while also minimizing the inconvenience to participants and maximizing data collection at operationally relevant timepoints. These are critical steps to collecting meaningful data in operational environments. The measures have been validated in both laboratory and field studies, which is important for interpreting results. Although the study was designed to enable participants to complete study procedures independently, the pre-study briefing session was crucial to ensure that volunteers understood the study procedures and importance of maintaining consistency when completing study tests and questions, particularly for the PVT.
The finding that sleep duration and timing changes according to work start time is consistent with prior studies in smaller samples of individuals that used PSG to evaluate sleep timing59,60. Although early starts and late finishes may be expected to encroach on sleep timing, the large sample of data collected in an operational environment provides insight into the unexpected ways that the participants lose sleep. For example, the wake maintenance zone, which represents the strongest drive to be awake, occurs just before a habitual bedtime. In laboratory studies, participants have been shown to have difficulty sleeping during the wake maintenance zone61,62,63. It was expected that participants may try to go to bed a few hours earlier than normal in order to prepare for early starts. It was also expected that as a result of trying to initiate sleep during the wake maintenance zone, participants may exhibit a long sleep latency during the sleep preceding early starts; however, this was not the case. These data highlight important differences between the laboratory and field, and they demonstrate the need for collecting sleep data in operational environments.
Although circadian phase information was obtained in a subset of individuals, the circadian phase changes observed in each schedule type mirrored the changes observed in sleep timing. The addition of the circadian phase to this protocol enhanced the ability to understand why fatigue ratings and performance changed by work start-time. Alertness and performance follow a circadian rhythm, with the lowest alertness and poorest performance typically coinciding with timing of the aMT6s acrophase. Although it was found that the circadian rhythms of most participants shifted in the expected direction relative to the imposed work schedule, it was also found that this shifting was variable between individuals. This suggests that some individuals may have more difficulty adapting to early or late schedules, causing modest circadian misalignment. The combination of these methods enhanced interpretation of these conclusions.
The sleep data collected also allowed for a better understanding of why fatigue ratings and performance changed relative to the different work schedules. For example, it was found that during early starts and late finishes, Samn-Perelli ratings and PVT performance was poorer by day on each of those schedules. This makes sense, because pilots obtained less sleep during early starts and late finishes relative to baseline, which meant that they were accruing sleep debt with each day on those schedules. In contrast, PVT performance was also poorer by day during the high workload mid-day start schedules. During the mid-day schedule, the amount of sleep the pilots obtained was not different from sleep duration during the baseline data collection. As a result, this finding suggests that the poorer performance observed during the mid-day work schedules was not likely to be driven by acute sleep restriction. It would have been very difficult to interpret the fatigue ratings and performance data without the sleep data, making the combination of these methods important.
Although these methods were designed and implemented successfully, this approach can involve some challenges. For example, it is possible that participants may forget when or how to complete some procedures. It is helpful to communicate with volunteers regularly to confirm that they are completing tasks according to the protocol, especially during the first phase of urine collection. In addition, the risk of data loss increases as the length of the study increases, because individuals may lose or damage their study devices. If a study is scheduled for several weeks, as was the case for this study, then it may be desirable to download data at the study midpoint to reduce potential data loss and review compliance with the protocol. Insufficient or missing data may reduce interpretability of the results, so care must be taken to ensure that individuals are collecting data appropriately.
There are many possible applications for these methods in other operational settings. These methods may be used to characterize sleep, circadian phase, fatigue, and performance in occupations with unusual scheduling practices or environmental considerations, such as during spaceflight or military operations. In addition, there are many promising interventions and countermeasures evaluated in laboratory environments, such as the use of blue-enriched light to accelerate circadian phase shifting, strategic on-the-job napping, hypnotics to maximize sleep opportunities, and stimulants such as caffeine to improve alertness. Although such approaches may be shown to be effective under controlled laboratory conditions, the deployment of such tools and technology in operational environments must be evaluated to confirm their efficacy in reducing fatigue in the real world. The combination of actigraphy, sleep diaries, circadian phase information, fatigue ratings, and PVT collection, combined with an easy-to-use software application to facilitate administration of tasks, provides adequate data for evaluating the effectiveness of interventions. The combination of these methods has significant translational potential for other complex operational environments, where it may be difficult to deploy more invasive data collection efforts.

Fatigue, arising from sleep loss and circadian misalignment, is a serious threat to safety in occupations that require 24 h operations, irregular schedules, and extended work hours1,2. Laboratory research has been instrumental in characterizing how changes in sleep duration and timing influence subsequent alertness and performance3,4,5. These studies form the basis for fatigue risk management recommendations and work scheduling practices in operational environments6.
In this manuscript, a field study of aviation operations is used to demonstrate an approach for collecting sleep, circadian, fatigue, and performance data in complex operational settings7. We studied 44 airline pilots over 34 days while they flew a schedule that included periods of mid-morning flights, early flights, high-workload mid-day flights, and late flights that landed after midnight. Each work block was separated by 3&#8211;4 days of rest. Pilots collected objective and subjective data over the entirety of the study period including both flight duty and rest days.
Given the differences between laboratory and real-world environments, implementation of strategies and countermeasures developed in the laboratory do not always translate into operations as expected. Individual differences, a broad range of operational work schedules, irregular and unpredictable operations, organizational practices and culture, and labor agreements are some of the factors that can complicate the application of science into practical operational use. As a result, it is important to evaluate the impact of such interventions using consistent and reliable methods to assess sleep, circadian rhythms, fatigue or alertness, and performance. The level of monitoring and data collecting must be kept proportional to the anticipated levels of fatigue and associated risks to safety within an operation8. Furthermore, in any safety-sensitive setting, maintaining safe operations is paramount to the investigatory protocol.
The gold standard method for assessing sleep duration and quality is through polysomnography (PSG), which involves measuring brain activity, heart rate, eye movement, and muscle activity through a collection of electrodes and sensors placed on the scalp, face, and chest. Although robust, PSG is not practical for collecting sleep information in most operational environments. Many wearable devices have been developed to estimate sleep timing, duration, and quality, but few have been validated9,10. The combination of wrist-worn actigraphy and daily sleep diaries have been widely used to estimate sleep in field studies across a range of occupations11,12,13,14 and have been validated against PSG, showing&#160;concordance for sleep duration15. In addition, using actigraphy and sleep diaries for field studies places a low burden of effort on study participants, because most actigraphy devices are worn on the non-dominant wrist and only removed for showering or swimming, much like a wristwatch. Likewise, a well-designed sleep diary, presented on a phone or touch-screen device, can typically be completed by participants in less than two min.
The sleep-wake cycle is coordinated by the circadian pacemaker located in the suprachiasmatic nuclei of the hypothalamus16. This pacemaker also synchronizes many other aspects of biological function such as body temperature and hormonal rhythms (e.g., melatonin and cortisol). The endogenous circadian rhythm is near to, but not exactly, 24 h; therefore, it must be reset each day to allow for stable synchronization (i.e., entrainment) to the 24 h day. The primary resetting agent of the circadian pacemaker is light. In operational environments that require non-standard schedules and 24 h operations, circadian misalignment can occur, in which the circadian drive to sleep coincides with scheduled work11. It is possible to determine when the circadian pacemaker is promoting sleep and wake by measuring the peak timing (i.e., circadian phase) of the rhythms of biological signals that are controlled by the circadian rhythm.
It is important to measure the circadian phase following implementation of countermeasures in order to better understand whether such techniques are successful in aligning the circadian pacemaker with the imposed work schedule. Many of the outputs of the circadian system used to determine phase in laboratory settings are prone to masking, making them unsuitable for use in a field environment. For example, circadian changes in body temperature are difficult to detect in free-living individuals who may engage in activities such as exercise that alters their body temperature. Melatonin is acutely suppressed by light exposure, making collection of melatonin in blood or saliva impossible in situations where light cannot be controlled. However, 6-sulfatoxymelatonin (aMT6s), the major metabolite of melatonin, is excreted in urine and is less affected by the masking effects of light, making it an ideal candidate for measuring the circadian phase in operational environments17,18.
In addition to measuring changes in physiology, it is also important to measure the impact of work schedule changes on subjective fatigue or alertness. While there are several scales available to measure different aspects of alertness and fatigue, the most commonly used in aviation are the 7-point Samn-Perelli Fatigue Scale (SP)19&#160;and 9-point Karolinska Sleepiness Scale (KSS)20. The SP is also commonly used in field studies of shift workers across a wide range of occupations21,22,23,24. The KSS has been validated against objective measures of sleepiness such as electroencephalography (EEG) and slow rolling eye movements20,25, as well as performance25. This scale is commonly used in studies both in the laboratory and the field24,26. There may be other subjective scales that are appropriate for different shiftwork or occupational environments. It is important to choose a scale that has been validated and ideally has meaningful thresholds for levels of &#8220;acceptable&#8221; alertness. For example, KSS scores over 7 are associated with high levels of physiological signs of sleepiness and impaired driving performance25,27, while Samn-Perelli ratings relate directly to flying duties28. For the study described in this manuscript, the Samn-Perelli was used, because it was originally developed as a subjective fatigue measure in a study population consisting of pilots.28
Although measuring sleep and circadian phase is an important component in evaluating an intervention, a primary outcome of interest in field studies is typically objective performance. There are a variety of tests that have been developed to evaluate cognitive performance, but the most sensitive and reliable test for measuring the effects of sleep loss and circadian misalignment is the Psychomotor Vigilance Task (PVT). The original PVT (PVT-192) is a simple reaction time test, where an individual is presented with a stimulus and is instructed to respond to the stimulus by pressing a button as quickly as possible29. The PVT has been validated under conditions of acute and chronic sleep loss and circadian misalignment4,5,30. The duration of the task can be varied based on the design of the study31,32; although, the traditional 10 min duration is preferred in laboratory studies33,34. while a 5 min duration PVT is typically more feasible in field studies where operational demands can interfere with the administration of the test35.
In addition, the PVT shows little to no learning effects and is simple to use, making it a practical test for deploying in field environments where study participants may not be observed during testing36. The ubiquity of touch-screen devices allows for easy deployment of the PVT, but researchers should be cautious when implementing the PVT, because there are numerous aspects of touch-screen devices that can introduce error into the collection of PVT data37,38. For example, different hardware and software combinations have different system latencies, and other applications running in the background can introduce unknown error into the recorded reaction times. As a result, it is important to collect PVT data using a validated PVT, with consistent hardware and software, with WiFi, and with all other applications turned off. In addition, given that it is not practical to observe study participants during tests in operational environments, it is critical that participants are trained to complete each PVT with the device in the same orientation, using the same finger38,39.
Each of these elements of data collection is important and these tools have been used in other operational studies in the past40,41,42,43. However, in addition to the challenges described above, it can be difficult to achieve compliance with study procedures when participants are required to independently complete tasks, especially when such tasks include a time-sensitive component. A final element that is important in data collection in operational environments is the organization of information in a way that makes it easy for individuals to complete tasks on time. The NASA PVT+ application for touchscreen devices can be customized to present tasks to participants in sequence, guiding them through study procedures. For example, in the study presented here, airline pilots are provided with touchscreen devices pre-loaded with an application that is used to complete sleep diaries every morning and evening. The devices are also used to complete PVT tests and fatigue ratings, among other tasks, in the morning, at the top-of-descent (TOD) of each flight, post-flight, and in the evening before bed. This presentation of information allowed pilots to complete study procedures with minimal inconvenience to their work-related tasks.
It can be very difficult to collect data among pilots, as the nature of the job requires them to travel long distances and work in confined spaces (i.e., cockpits) with many distractions and often unpredictable workloads. Despite these challenges, it is critical to collect data in this population, because pilot fatigue is a threat to safe aviation operations40,44,45. The high intensity of airline operations is conducive to degradation of crew performance and increases the risk of fatigue-related incidents46,47,48,49,50. Using the combination of methods described above, we measured sleep, circadian rhythms, fatigue and performance among 44 short-haul airline pilots over 34 days. During the study, pilots flew a fixed schedule that included a baseline data collection with 5 days of mid-morning flights, four early flights, four high-workload mid-day flights, and four late flights landing after midnight. Each work block was separated by 3&#8211;4 days of rest. These findings demonstrate how comprehensive data collection, including measures of sleep, circadian rhythms, fatigue, and performance, can be used in operational environments.
In this case, the purpose of the study was to evaluate sleep, circadian rhythms, fatigue, and performance by duty start time as follows. 1) Baseline: during the first duty block, all pilots worked 5 days that each included two flights of about 2 h each, starting in the mid-morning, to allow for an adequate nighttime sleep episode. This block was followed by 4 rest days. 2) Early starts: during the early duty block, all pilots worked 5 days that each included two flights of about 2 h, each starting between approximately 5:00 AM and 8:00 AM. This block was followed by 3 rest days. 3) High-workload shifts mid-day: during the mid-day duty block, all pilots worked 5 days, which each included 2&#8211;4 flights of ~2&#8211;6 h each, starting at approximately mid-day. This block was followed by 3 rest days. 4) Late finishes: during the late duty block, all pilots worked 5 days, which included two flights of about 3 h each, starting in the late afternoon around 4:00 PM and ending around midnight. This block was followed by 3 rest days.

<table>
	<tbody>
		<tr>
			<td>Actiwatch Spectrum Pro</td>
			<td>Philips Respironics, Bend OR, USA</td>
			<td>1099351</td>
			<td>The number listed in the Catalog Number section is the Reference number for Actiwatch Spectrum Pro.</td>
		</tr>
		<tr>
			<td>iPod Touch 5Th gen</td>
			<td>Apple Inc., Cupertino CA, USA</td>
			<td>A1509</td>
			<td>The number listed in the Catalog Number section is the Model number. Newer generations of iPods can be used for data collection.</td>
		</tr>
		<tr>
			<td>Medline DYND30261 Zip-Style Biohazard Specimen Bags, Plastic, Latex Free, 9&#34; Length, 6&#34; Width, Clear</td>
			<td>Medline Industries, Inc., Northfield IL</td>
			<td>DYND30261</td>
			<td>The number listed in the catalog Number section is the Part number</td>
		</tr>
		<tr>
			<td>Medline DYND80024 24 hours Urine Collection Bottle, 3000 mL</td>
			<td>Medline Industries, Inc., Northfield IL</td>
			<td>DYND80024</td>
			<td>The number listed in the catalog Number section is the Part number</td>
		</tr>
		<tr>
			<td>Moveland 3ml Disposable Plastic Transfer Pipettes</td>
			<td>Moveland</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Nordic Ice NOR1038 No-Sweat Reusable Long-Lasting Gel Pack, 16 oz. (Pack of 3)</td>
			<td>Nordic Cold Chain Solutions</td>
			<td>0858687005050</td>
			<td></td>
		</tr>
		<tr>
			<td>Office Depot Brand Print-Or-Write Color Permanent Inkjet/Laser File Folder Labels, OD98817, 5/8&#34; x 3 1/2&#34;, Dark Blue</td>
			<td>Office Depot, Inc.Boca Raton FL, USA</td>
			<td>660-426</td>
			<td></td>
		</tr>
		<tr>
			<td>Philips Actiware 6.0.9</td>
			<td>Respironics, Inc., Murrysville PA, USA</td>
			<td>1104776</td>
			<td>This software is used to analyze sleep recorded through Actiwatch Spectrum Pro</td>
		</tr>
		<tr>
			<td>Push cap, neutral for 7 mL tubes</td>
			<td>Sarstedt, Numbrecht, Germany</td>
			<td>65.793</td>
			<td></td>
		</tr>
		<tr>
			<td>SAS software 9.4</td>
			<td>SAS Institute, Cary, NC</td>
			<td>https://www.sas.com/en_us/software/visual-statistics.html</td>
			<td>This software is used to analyze the data. Any statistical software (e.g., SPSS, R) can be used.</td>
		</tr>
		<tr>
			<td>Shipping material</td>
			<td>FedEx, USPS, UPS</td>
			<td></td>
			<td>Any company can be used.</td>
		</tr>
		<tr>
			<td>Specimen Collector Urine/Stool White 26 oz.</td>
			<td>McKesson Corporation, San Francisco CA</td>
			<td>16-9522</td>
			<td>The number listed in the catalog Number section is the Part number</td>
		</tr>
		<tr>
			<td>Tube 7 mL, 50x16mm, PS</td>
			<td>Sarstedt, Numbrecht, Germany</td>
			<td>58.485</td>
			<td></td>
		</tr>
	</tbody>
</table>

collecting sleep, circadian, fatigue, and performance data in complex operational environments

Sleep loss and circadian misalignment contribute to a meaningful proportion of operational accidents and incidents. Countermeasures and work scheduling designs aimed at mitigating fatigue are typically evaluated in controlled laboratory environments, but the effectiveness of translating such strategies to operational environments can be challenging to assess. This manuscript summarizes an approach for collecting sleep, circadian, fatigue, and performance data in a complex operational environment. We studied 44 airline pilots over 34 days while they flew a fixed schedule, which included a baseline data collection with 5 days of mid-morning flights, four early flights, four high-workload mid-day flights, and four late flights that landed after midnight. Each work block was separated by 3&#8211;4 days of rest. To assess sleep, participants wore a wrist-worn research-validated activity monitor continuously and completed daily sleep diaries. To assess the circadian phase, pilots were asked to collect all urine produced in four or eight hourly bins during the 24 h after each duty block for the assessment of 6-sulfatoxymelatonin (aMT6s), which is a biomarker of the circadian rhythm. To assess subjective fatigue and objective performance, participants were provided with a touch-screen device used to complete the Samn-Perelli Fatigue Scale and Psychomotor Vigilance Task (PVT) during and after each flight, and at waketime, mid-day, and bedtime. Using these methods, it was found that sleep duration was reduced during early starts and late finishes relative to baseline. Circadian phase shifted according to duty schedule, but there was a wide range in the aMT6s peak between individuals on each schedule. PVT performance was worse on the early, high-workload, and late schedules relative to baseline. Overall, the combination of these methods was practical and effective for assessing the influence of sleep loss and circadian phase on fatigue and performance in a complex operational environment.

Using the methods described, we were able to collect over 700 days of data and over 3,000 PVTs and fatigue ratings among 44 short-haul pilots7. The goal of this study was to characterize changes in sleep, circadian phase, fatigue ratings, and performance among short-haul pilots by work start-time and workload during daytime flights.
To account for the within-subjects study design, all condition effects were evaluated for sleep and performance outcomes using repeated measures analysis of variance with unstructured covariances, using participant as a repeated factor. To evaluate whether sleep and performance outcomes varied by day on a given schedule, linear mixed effects models were applied to the changes in sleep and performance by day. To account for individual differences in adaptation to a given schedule, the intercept and slope were allowed to vary by individual.
The first objective addressed with these methods was to examine the impact of duty start time on sleep. Sleep duration, bedtime, wake time, and sleep quality were calculated using the sleep diary and actigraphy. An example of the actogram derived from activity monitor is illustrated in Figure 7. It was demonstrated that sleep timing and duration varied significantly as a function of work start time using mixed-effects regression analysis. Table 1 displays the bedtime, wake time, sleep duration and sleep quality by schedule type&#160;as reported by participants in the sleep diary. Participants went to bed on average at around 23:10 (SD = 1:41) on baseline block. The bedtime for early duty schedule block differed significantly from baseline (p &#60; 0.01) with participants reporting earlier bedtimes. The bedtimes for mid-day and late duty schedules also differed significantly from baseline (p &#60; 0.01), with participants reporting later bedtimes. Participants went to bed significantly later (p &#60; 0.01) on rest days compared to baseline.
Figure 8 displays the mean-actigraphy derived sleep duration by day for each schedule type. Participants obtained significantly less sleep (p &#60; 0.01) on early starts compared to baseline. The sleep duration on the other schedule types were not different from baseline. Sleep latency and sleep efficiency obtained from actigraphy were not significantly different from baseline for any of the schedule types. Wake after sleep onset (WASO) was significantly different for early starts compared to baseline (p &#60; 0.05), with pilots reporting being more awake during the early starts. There were no differences between the baseline and other schedule types. There were no significant differences between rest days and the baseline.
The second objective addressed with these methods was to examine the impact of duty start time on circadian phase as measured by aMT6s. The peak timing (acrophase) of the aMT6s rhythm is a reliable marker of circadian phase58. Figure 9 shows an example of the circadian rhythm of aMT6s over 24 h for one individual, while Figure 10 shows the aMT6s acrophase for each individual who participated in the urine collection procedures by study block. Consistent with the findings on sleep, it was found that mean circadian phase was significantly shifted according to work start time. It is important to note the missing data collection information in Figure 10. Some individuals had difficulty with the urine collection procedures for some of the blocks or they forgot to log the timing of their sample collection. In these cases, it was not possible to generate reliable estimates of circadian phase from the aMT6s concentration and as a result some data are missing. In situations where collection of circadian phase information is important, it may be prudent to call participants prior to each urine collection to ensure the procedures are properly followed.
The third objective addressed with these methods was to examine the impact of duty start time on self-reported fatigue as measured by SP, and objective performance as measured by the PVT. Consistent with our findings with sleep, using mixed-effects regression analysis, we found that both fatigue (Table 2) and PVT reaction times (Figure 11) were worse during early starts, high workload mid-day shifts, and late finishes, relative to our baseline data collection (p &#60; 0.001 SP; p &#60; 0.01 PVT RT). Participants showed a significant increase in lapses for each schedule type compared to baseline (p &#60; 0.01 early; p &#60; 0.05 mid-day; p &#60; 0.01 late). Performance on rest days was similar to that of the baseline. These results are also described in Table 3.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/59851/59851fig01.jpg" /> 
Figure 1: Study protocol by time of day for each day of the study.&#160;The dark gray bars represent the flight periods including the pre-flight report time (open bars), and the light gray bars represent the sleep periods. Days 1&#8211;5 represent the baseline duty block, days 10&#8211;14 represent the early duty starts, days 18&#8211;22 represent the mid-day duty starts, and days 26&#8211;30 represent the late starts. The shaded bars represent the first rest day post duty block when urine is collected. This figure is reproduced from Flynn-Evans et al.7. <a href="https://www.jove.com/files/ftp_upload/59851/59851fig01large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/59851/59851fig02.jpg" /> 
Figure 2: The activity monitor/accelerometer device worn on the wrist of the non-dominant hand. <a href="https://www.jove.com/files/ftp_upload/59851/59851fig02large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/59851/59851fig03.jpg" /> 
Figure 3: Example of tests taken during rest days using the touchscreen application.&#160;From left to right: (A) the main page of the app displays two links; (B) the rest day displays three links: morning, mid-day, evening; (C) the morning link displays the tests taken in the morning; (D) the mid-day link displays the tests taken in the afternoon, and (E) the evening link displays the test taken in the evening. <a href="https://www.jove.com/files/ftp_upload/59851/59851fig03large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" class="xfigimg" src="/files/ftp_upload/59851/59851fig04.jpg" /> 
Figure 4: Urine kit.&#160;The kit contains (A) a urinal hat or urinal collection container, (B) pipettes, (C) urine collection tube, (D) white sticker labels, (E) a bio-hazard bag, (F) ice pack, and (G) shipping materials. <a href="https://www.jove.com/files/ftp_upload/59851/59851fig04large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 5" class="xfigimg" src="/files/ftp_upload/59851/59851fig05.jpg" /> 
Figure 5: Example of the urine collection log.
<img alt="Figure 6" class="xfigimg" src="/files/ftp_upload/59851/59851fig06.jpg" /> 
Figure 6: Psychomotor Vigilance Task (PVT).&#160;(A) The touchscreen device is oriented in landscape position and the thumbs are displayed on the screen at the beginning of the test. (B) the reaction times are displayed on a rectangular box in the upper middle part of the screen. <a href="https://www.jove.com/files/ftp_upload/59851/59851fig06large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 7" class="xfigimg" src="/files/ftp_upload/59851/59851fig07.jpg" /> 
Figure 7: Actogram of sleep-wake cycles over 24 h for 14 days.&#160;The dark blue color represents the sleep periods; the light blue represents the rest periods. The black color represents movement. The yellow color represents the light. <a href="https://www.jove.com/files/ftp_upload/59851/59851fig07large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 8" class="xfigimg" src="/files/ftp_upload/59851/59851fig08.jpg" /> 
Figure 8: Mean actigraphy-derived sleep duration by day on each schedule type.&#160;Day 1 represents the night of sleep before the first work period of a given block. An asterisk designates a significant difference (*p &#60; 0.05, **p &#60; 0.01) in the means between the baseline condition and early starts block. <a href="https://www.jove.com/files/ftp_upload/59851/59851fig08large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 9" class="xfigimg" src="/files/ftp_upload/59851/59851fig09.jpg" /> 
Figure 9: aMT6 profile for the five urine collection bins for each data collection episode for a single participant.&#160;Data are double-plotted. <a href="https://www.jove.com/files/ftp_upload/59851/59851fig09large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 10" class="xfigimg" src="/files/ftp_upload/59851/59851fig10.jpg" /> 
Figure 10: 6-sulfatoxymelatonin (aMT6) acrophase (peak) by time (24 h clock) of circadian nadir and schedule type for each individual.&#160;Filled and open circles, triangles, squares represent individual participants. This figure is reproduced from Flynn-Evans et al.7 <a href="https://www.jove.com/files/ftp_upload/59851/59851fig10large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 11" class="xfigimg" src="/files/ftp_upload/59851/59851fig11.jpg" /> 
Figure 11: Psychomotor Vigilance Task (PVT) mean reaction time (RT), lapses (RT &#62;500ms), and response speed (mean 1/RT) by day on each schedule type.&#160;Asterisks following each slope indicate changes in performance by day in that condition. Brackets indicate differences in the slope between baseline performance and the slope in performance in each of the other conditions (*p &#60; 0.05, **p &#60; 0.01). Baseline = filled circles, early = open circles, mid-day = filled triangles, late = open triangles. <a href="https://www.jove.com/files/ftp_upload/59851/59851fig11large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Work schedule</td>
			<td>n</td>
			<td>Bedtime (h, SD)</td>
			<td>Wake time (h, SD)</td>
			<td>Sleep duration (h, SD)</td>
			<td>Sleep quality (SD)</td>
		</tr>
		<tr>
			<td>Baseline (ref.)</td>
			<td>39</td>
			<td>23:10 (1:41)</td>
			<td>7:20 (1:49)</td>
			<td>8.2 (0.9)</td>
			<td>2.4 (0.7)</td>
		</tr>
		<tr>
			<td>Early</td>
			<td>42</td>
			<td>21:14 (1:01)**</td>
			<td>4:29 (0:47)</td>
			<td>7.4 (0.9)**</td>
			<td>2.5 (0.6)</td>
		</tr>
		<tr>
			<td>Midday</td>
			<td>41</td>
			<td>01:19 (0:43)**</td>
			<td>9:11 (0:58)</td>
			<td>7.9 (1.1)</td>
			<td>2.3 (0.6)</td>
		</tr>
		<tr>
			<td>Late</td>
			<td>40</td>
			<td>02:18 (1:07)**</td>
			<td>9:57 (1:11)</td>
			<td>7.8 (1.4)*</td>
			<td>2.3 (0.7)</td>
		</tr>
		<tr>
			<td>Rest days</td>
			<td>42</td>
			<td>23:47 (0:50)**</td>
			<td>8:16 (0:58)</td>
			<td>8.5 (0.9)*</td>
			<td>2.4 (0.5)</td>
		</tr>
	</tbody>
</table>
Table 1: Sleep diary-derived sleep outcomes (bedtime, wake time, sleep duration and sleep quality) by schedule type.&#160;*p &#60; 0.05, **p &#60; 0.01; h = hour, SD = standard deviation. This table is reproduced from Flynn-Evans et al.7
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Work schedule</td>
			<td>Mean (SD)</td>
			<td>p-value</td>
		</tr>
		<tr>
			<td>Baseline</td>
			<td>3.51 (0.80)</td>
			<td>ref.</td>
		</tr>
		<tr>
			<td>Early duty</td>
			<td>4.03 (0.88)</td>
			<td>&#60; 0.001</td>
		</tr>
		<tr>
			<td>Midday duty</td>
			<td>3.85 (0.90)</td>
			<td>&#60; 0.001</td>
		</tr>
		<tr>
			<td>Late duty</td>
			<td>3.85 (0.89)</td>
			<td>&#60; 0.001</td>
		</tr>
	</tbody>
</table>
Table 2: Means and standard deviation for Samn-Perelli (SP) scores by duty block.&#160;A higher rating indicates greater fatigue.
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Work schedule</td>
			<td>n (participants)</td>
			<td>Mean reaction time (ms, SD)</td>
			<td>Response speed (s, SD)</td>
			<td>Mean Lapses (&#62; 500 ms)</td>
		</tr>
		<tr>
			<td>Baseline (ref.)</td>
			<td>38</td>
			<td>236 (48)</td>
			<td>4.84 (0.61)</td>
			<td>3.1 (4.1)</td>
		</tr>
		<tr>
			<td>Early</td>
			<td>40</td>
			<td>257 (70)**</td>
			<td>4.63 (0.66)**</td>
			<td>4.4 (5.4)**</td>
		</tr>
		<tr>
			<td>Midday</td>
			<td>39</td>
			<td>261 (62)**</td>
			<td>4.56 (0.66)**</td>
			<td>4.7 (5.1)*</td>
		</tr>
		<tr>
			<td>Late</td>
			<td>38</td>
			<td>266 (64)**</td>
			<td>4.51 (0.63)**</td>
			<td>4.7 (5.0)**</td>
		</tr>
		<tr>
			<td>Rest days</td>
			<td>40</td>
			<td>249 (56)</td>
			<td>4.69 (0.62)</td>
			<td>4.0 (4.5)</td>
		</tr>
	</tbody>
</table>
Table 3: Psychomotor Vigilance Task (PVT) mean reaction time (RT), response speed (mean 1/RT), and lapses (RT &#62; 500 ms) by schedule type.&#160;*p &#60; 0.05, **p &#60; 0.01; this table is reproduced from Flynn-Evans et al.7

Watch this Scientific Journal Video about Collecting Sleep, Circadian, Fatigue, and Performance Data in Complex Operational Environments at JoVE.com

Collecting Sleep, Circadian, Fatigue, and Performance Data in Complex Operational Environments

Sleep loss and circadian misalignment contribute to numerous operational accidents and incidents. The effectiveness of countermeasures and work scheduling designs aimed at mitigating fatigue can be challenging to evaluate in operational environments. This manuscript summarizes an approach for collecting sleep, circadian, fatigue, and performance data in complex operational environments.

Sleep loss and circadian misalignment contribute to a meaningful proportion of operational accidents and incidents. Countermeasures and work scheduling ...

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Assessing Functional Performance in the Mdx Mouse Model

Duchenne muscular dystrophy (DMD) is a severe and progressive muscle wasting disorder for which no cure is available. Nevertheless, several potential pharmaceutical compounds and gene therapy approaches have progressed into clinical trials. With improvement in muscle function being the most important end point in these trials, a lot of emphasis has been placed on setting up reliable, reproducible, and easy to perform functional tests to pre clinically assess muscle function, strength, condition, and coordination in the mdx mouse model for DMD. Both invasive and noninvasive tests are available. Tests that do not exacerbate the disease can be used to determine the natural history of the disease and the effects of therapeutic interventions (e.g. forelimb grip strength test, two different hanging tests using either a wire or a grid and rotarod running). Alternatively, forced treadmill running can be used to enhance disease progression and/or assess protective effects of therapeutic interventions on disease pathology. We here describe how to perform these most commonly used functional tests in a reliable and reproducible manner. Using these protocols based on standard operating procedures enables comparison of data between different laboratories.

Assessing Functional Performance in the Mdx Mouse Model

The primary outcome measure in clinical trials for neuromuscular disorders is generally improved muscle function. Therefore, assessing the effect of potential therapeutic compounds on muscle performance pre clinically in mouse models is of great importance. We here describe several functional tests to address this.

Duchenne muscular dystrophy (DMD) is a severe and progressive muscle wasting disorder for which no cure is available. Nevertheless, several potential ...

Eye Tracking, Cortisol, and a Sleep vs. Wake Consolidation Delay: Combining Methods to Uncover an Interactive Effect of Sleep and Cortisol on Memory

Although rises in cortisol can benefit memory consolidation, as can sleep soon after encoding, there is currently a paucity of literature as to how these two factors may interact to influence consolidation. Here we present a protocol to examine the interactive influence of cortisol and sleep on memory consolidation, by combining three methods: eye tracking, salivary cortisol analysis, and behavioral memory testing across sleep and wake delays. To assess resting cortisol levels, participants gave a saliva sample before viewing negative and neutral objects within scenes. To measure overt attention, participants&#8217; eye gaze was tracked during encoding. To manipulate whether sleep occurred during the consolidation window, participants either encoded scenes in the evening, slept overnight, and took a recognition test the next morning, or encoded scenes in the morning and remained awake during a comparably long retention interval. Additional control groups were tested after a 20&#160;min&#160;delay in the morning or evening, to control for time-of-day effects. Together, results showed that there is a direct relation between resting cortisol at encoding and subsequent memory, only following a period of sleep. Through eye tracking, it was further determined that for negative stimuli, this beneficial effect of cortisol on subsequent memory may be due to cortisol strengthening the relation between where participants look during encoding and what they are later able to remember. Overall, results obtained by a combination of these methods uncovered an interactive effect of sleep and cortisol on memory consolidation.

We present a protocol used to discover an interactive effect between sleep and cortisol on memory consolidation, particularly for negative arousing images. Specifically, the experimental design utilizes eye tracking, salivary cortisol analysis, and behavioral memory testing &#8211; methods that can be used with both healthy and clinical participants.

Although rises in cortisol can benefit memory consolidation, as can sleep soon after encoding, there is currently a paucity of literature as to how these ...

Multifunctional Setup for Studying Human Motor Control Using Transcranial Magnetic Stimulation, Electromyography, Motion Capture, and Virtual Reality

The study of neuromuscular control of movement in humans is accomplished with numerous technologies. Non-invasive methods for investigating neuromuscular function include transcranial magnetic stimulation, electromyography, and three-dimensional motion capture. The advent of readily available and cost-effective virtual reality solutions has expanded the capabilities of researchers in recreating &#8220;real-world&#8221; environments and movements in a laboratory setting. Naturalistic movement analysis will not only garner a greater understanding of motor control in healthy individuals, but also permit the design of experiments and rehabilitation strategies that target specific motor impairments (e.g. stroke). The combined use of these tools will lead to increasingly deeper understanding of neural mechanisms of motor control. A key requirement when combining these data acquisition systems is fine temporal correspondence between the various data streams. This protocol describes a multifunctional system&#8217;s overall connectivity, intersystem signaling, and the temporal synchronization of recorded data. Synchronization of the component systems is primarily accomplished through the use of a customizable circuit, readily made with off the shelf components and minimal electronics assembly skills.

Transcranial magnetic stimulation, electromyography, and 3D motion capture are commonly used non-invasive techniques for investigating neuromuscular function in humans. In this paper, we describe a protocol that synchronously samples data generated by all three of these tools along with the unique addition of virtual reality stimulus presentation and feedback.

The study of neuromuscular control of movement in humans is accomplished with numerous technologies. Non-invasive methods for investigating neuromuscular ...

The Treadmill Fatigue Test: A Simple, High-throughput Assay of Fatigue-like Behavior for the Mouse

Fatigue is a prominent symptom in many diseases and disorders and reduces quality of life for many people. The lack of clear pathogenesis and failure of current interventions to adequately treat fatigue in all patients leaves a need for new treatment options. Despite the therapeutic need and importance of preclinical research in helping identify promising novel treatments, few preclinical assays of fatigue are available. Moreover, the most common preclinical assay used to assess fatigue-like behavior, voluntary wheel running, is not suitable for use with some strains of mice, may not be sensitive to drugs that reduce fatigue, and has relatively low throughput. The current protocol describes a novel, non-voluntary preclinical assay of fatigue-like behavior, the treadmill fatigue test, and provides evidence of its efficacy in detecting fatigue-like behavior in mice treated with a chemotherapy drug known to cause fatigue in humans and fatigue-like behavior in animals. This assay may be a beneficial alternative to wheel running, as fatigue-like behavior and potential interventions can be assessed in a greater number of mice over a shorter time frame, thus permitting faster discovery of new therapeutic options.

Fatigue is a common, undertreated and frequently poorly-understood symptom in many diseases and disorders. New preclinical assays of fatigue may help to improve current understanding and future treatment of fatigue. To that end, the current protocol provides a novel means of measuring fatigue-like behavior in the mouse.

Fatigue is a prominent symptom in many diseases and disorders and reduces quality of life for many people. The lack of clear pathogenesis and failure of ...

Manipulation of Epileptiform Electrocorticograms (ECoGs) and Sleep in Rats and Mice by Acupuncture

Ancient Chinese literature has documented that acupuncture possesses efficient therapeutic effects on epilepsy and insomnia. There is, however, little research to reveal the possible mechanisms behind these effects. To investigate the effect of acupuncture on epilepsy and sleep, several issues need to be addressed. The first is to identify the acupoints, which correspond between humans, rats, and mice. Furthermore, the depth of insertion of the acupuncture needle, the degree of needle twist in manual needle acupuncture, and the stimulation parameters for electroacupuncture (EA) need to be determined. To evaluate the effects of acupuncture on epilepsy and sleep, a feasible model of epilepsy in rodents is required. We administer pilocarpine into the left central nucleus of the amygdala (CeA) to simulate focal temporal lobe epilepsy (TLE) in rats. Intraperitoneal (IP) injection of pilocarpine induces generalized epilepsy and status epilepticus (SE) in rats. Five IP injections of pentylenetetrazol (PTZ) with a one-day interval between each injection successfully induces spontaneous generalized epilepsy in mice. Recordings of electrocorticograms (ECoGs), electromyograms (EMGs), brain temperature, and locomotor activity are used for sleep analysis in rats, while ECoGs, EMGs, and locomotor activity are employed for sleep analysis in mice. ECoG electrodes are implanted into the frontal, parietal, and contralateral occipital cortices, and a thermistor is implanted above the cerebral cortex by stereotactic surgery. EMG electrodes are implanted into the neck muscles, and an infrared detector determines locomotor activity. The criteria for categorizing vigilance stages, including wakefulness, rapid eye movement (REM) sleep, and non-REM (NREM) sleep are based on information from ECoGs, EMGs, brain temperature, and locomotor activity. Detailed classification criteria are stated in the text.

Manipulation of Epileptiform Electrocorticograms ECoGs and Sleep in Rats and Mice by Acupuncture

This paper demonstrates the performance of acupuncture, epilepsy models, and the analysis of sleep in rodents. The acupuncture procedure and the identification of acupoints are described. Pilocarpine or pentylenetetrazol (PTZ) is used to induce epilepsy. Electrocorticogram (ECoG), electromyogram (EMG), brain temperature, and locomotor activity recordings are employed for sleep analysis.

Ancient Chinese literature has documented that acupuncture possesses efficient therapeutic effects on epilepsy and insomnia. There is, however, little ...

A Computational Method to Quantify Fly Circadian Activity

In most animals and plants, circadian clocks orchestrate behavioral and molecular processes and synchronize them to the daily light-dark cycle. Fundamental mechanisms that underlie this temporal control are widely studied using the fruit fly Drosophila melanogaster as a model organism. In flies, the clock is typically studied by analyzing multiday locomotor recording. Such a recording shows a complex bimodal pattern with two peaks of activity: a morning peak that happens around dawn, and an evening peak that happens around dusk. These two peaks together form a waveform that is very different from sinusoidal oscillations observed in clock genes, suggesting that mechanisms in addition to the clock have profound effects in producing the observed patterns in behavioral data. Here we provide instructions on using a recently developed computational method that mathematically describes temporal patterns in fly activity. The method fits activity data with a model waveform that consists of four exponential terms and nine independent parameters that fully describe the shape and size of the morning and evening peaks of activity. The extracted parameters can help elucidate the kinetic mechanisms of substrates that underlie the commonly observed bimodal activity patterns in fly locomotor rhythms.

A method to quantify the main temporal features seen in fly circadian locomotor rhythms is presented. The quantification is achieved by fitting fly activity with a multi-parametric model waveform. The model parameters describe the shape and size of the morning and evening peaks of daily activity.

In most animals and plants, circadian clocks orchestrate behavioral and molecular processes and synchronize them to the daily light-dark cycle. ...

Noninvasive, High-throughput Determination of Sleep Duration in Rodents

Traditionally, sleep is monitored by an electroencephalogram (EEG). EEG studies in rodents require surgical implantation of the electrodes followed by a long recovery period. To perform an EEG recording, the animal is connected to a receiver, creating an unnatural tether to the head-mount. EEG monitoring is time consuming, carries risk to the animal, and is not a completely natural setting for the measurement of sleep. Alternative methods to detect sleep, particularly in a high-throughput fashion, would greatly advance the field of sleep research. Here, we describe a validated method for detecting sleep via activity-based home-cage monitoring. Previous studies have shown that sleep assessed via this method has a high degree of agreement with sleep defined by traditional EEG-based measures. Whereas this method is validated for total sleep time, it is important to note that sleep bout duration should be assessed by an EEG which has better temporal resolution. The EEG can also differentiate rapid eye movement (REM) and non-REM sleep, giving more detail about the exact nature of sleep. Nevertheless, activity-based sleep determination can be used to analyze multiple days of undisturbed sleep and to assess sleep as a response to an acute event (like stress). Here, we show the power of this system to detect the response of mice to daily intraperitoneal injections.

We describe a high-throughput method of measuring sleep by means of activity-based home-cage monitoring. This method offers advantages over traditional EEG-based methods. It is well validated for the determination of total sleep duration and can be a powerful tool to monitor sleep in rodent models of human disease.

Traditionally, sleep is monitored by an electroencephalogram (EEG). EEG studies in rodents require surgical implantation of the electrodes followed by a ...

A High-performance Liquid Chromatography Measurement of Kynurenine and Kynurenic Acid: Relating Biochemistry to Cognition and Sleep in Rats

The kynurenine pathway (KP) of tryptophan degradation has been implicated in psychiatric disorders. Specifically, the astrocyte-derived metabolite kynurenic acid (KYNA), an antagonist at both N-methyl-d-aspartate (NMDA) and &#945;7 nicotinic acetylcholine (&#945;7nACh) receptors, has been implicated in cognitive processes in health and disease. As KYNA levels are elevated in the brains of patients with schizophrenia, a malfunction at the glutamatergic and cholinergic receptors is believed to be causally related to cognitive dysfunction, a core domain of the psychopathology of the illness. KYNA may play a pathophysiologically significant role in individuals with schizophrenia. It is possible to elevate endogenous KYNA in the rodent brain by treating animals with the direct bioprecursor kynurenine, and preclinical studies in rats have demonstrated that acute elevations in KYNA may impact their learning and memory processes. The current protocol describes this experimental approach in detail and combines a) a biochemical analysis of blood kynurenine levels and brain KYNA formation (using high-performance liquid chromatography), b) behavioral testing to probe the hippocampal-dependent contextual memory (passive avoidance paradigm), and c) an assessment of sleep-wake behavior [telemetric recordings combining electroencephalogram (EEG) and electromyogram (EMG) signals] in rats. Taken together, a relationship between elevated KYNA, sleep, and cognition is studied, and this protocol describes in detail an experimental approach to understanding function outcomes of kynurenine elevation and KYNA formation in vivo in rats. Results obtained through variations of this protocol will test the hypothesis that the KP and KYNA serve pivotal roles in modulating sleep and cognition in health and disease states.

Alterations in the kynurenine pathway (KP) neuroactive metabolites are implicated in psychiatric illnesses. Investigating the functional outcomes of an altered kynurenine pathway metabolism in vivo in rodents may help elucidate novel therapeutic approaches. The current protocol combines biochemical and behavioral approaches to investigate the impact of an acute kynurenine challenge in rats.

The kynurenine pathway (KP) of tryptophan degradation has been implicated in psychiatric disorders. Specifically, the astrocyte-derived metabolite ...

Chronic Sleep Deprivation in Mouse Pups by Means of Gentle Handling

Sleep is critical for proper development and neural plasticity. Moreover, abnormal sleep patterns are characteristic of many neurodevelopmental disorders. Studying how chronic sleep restriction during development can affect adult behavior may add to our understanding of the emergence of behavioral symptoms of neurodevelopmental disorders. While there are many methods that can be used to restrict sleep in rodents including forced locomotion, constant disruption, presentation of an aversive stimulus, or electric shock, many of these methods are very stressful and cannot be used in neonatal mice. Here, we describe gentle handling, a sleep deprivation technique that can be used chronically throughout development and into adulthood to achieve sleep restriction. Gentle handling involves close observation of the mice throughout the sleep deprivation period and requires the researcher to gently prod the animals whenever they are inactive or display behaviors associated with sleep. Coupled with EEG recordings, gentle handling could be used to selectively disrupt a specific phase of sleep such as rapid eye movement (REM) sleep. The technique of gentle handling is a powerful tool for the study of the effects of chronic sleep restriction even in neonatal mice that circumvents many of the more stressful procedures used for sleep deprivation.

We describe a sleep deprivation technique known as gentle handling where investigators gently prod mice any time sleep behavior is observed. This method is a powerful tool that allows researchers to study the effects that chronic sleep restriction throughout development can have on future brain physiology and behavior.

Sleep is critical for proper development and neural plasticity. Moreover, abnormal sleep patterns are characteristic of many neurodevelopmental disorders. ...

Automated Measurements of Sleep and Locomotor Activity in Mexican Cavefish

Across phyla, sleep is characterized by highly conserved behavioral characteristics that include elevated arousal threshold, rebound following sleep deprivation, and consolidated periods of behavioral immobility. The Mexican cavefish, Astyanax mexicanus (A. mexicanus), is a model for studying trait evolution in response to environmental perturbation. A. mexicanus exist as in eyed surface-dwelling forms and multiple blind cave-dwelling populations that have robust morphological and behavioral differences. Sleep loss has occurred in multiple, independently-evolved cavefish populations. This protocol describes a methodology for quantifying sleep and locomotor activity in A. mexicanus cave and surface fish. A cost-effective video monitoring system allows for behavioral imaging of individually-housed larval or adult fish for periods of a week or longer. The system can be applied to fish aged 4 days post fertilization through adulthood. The approach can also be adapted for measuring the effects of social interactions on sleep by recording multiple fish in a single arena. Following behavioral recordings, data is analyzed using automated tracking software and sleep analysis is processed using customized scripts that quantify multiple sleep variables including duration, bout length, and bout number. This system can be applied to measure sleep, circadian behavior, and locomotor activity in almost any fish species including zebrafish and sticklebacks.

This protocol details the methodology for quantifying locomotor behavior and sleep in the Mexican cavefish. Previous analyses are extended to measure these behaviors in socially-housed fish. This system can be widely applied to study sleep and activity in other fish species.

Across phyla, sleep is characterized by highly conserved behavioral characteristics that include elevated arousal threshold, rebound following sleep ...