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Free-running sleep experiments can involve any organism which sleeps. Freerunning sleep is sleep which is not adjusted, entrained, to the 24-hour cycle in nature nor to any artificial cycle. Such experiments are used in the study of circadian and other rhythms in biology. Subjects are shielded from all time cues, often by a constant light protocol, by a constant dark protocol or by the use of light/dark conditions to which the organism cannot entrain such as the ultrashort protocol of one hour dark and two hours light. Also, limited amounts of food can be made available at short intervals so as to avoid entrainment to mealtimes. Subjects are thus forced to live by their internal circadian "clocks".

The individual's or animal's circadian phase can be known only by the monitoring of some kind of output of the circadian system, the internal "body clock". The researcher can precisely determine, for example, the daily cycles of gene-activity, body temperature, blood pressure, hormone secretion and/or sleep and activity/alertness. Alertness in humans can be determined by many kinds of verbal and non-verbal tests; activity in animals by observation, for example of wheel-running in rodents.

When animals or people freerun, experiments can be done to see what sort of signals, known as zeitgeber, are effective in entrainment. Also, much work has been done to see how long or short a circadian cycle the different organisms can be entrained to. For example, some animals can be entrained to a 22-hour day, but they can not be entrained to a 20-hour day. In recent studies funded by the U.S. space industry, it has been shown that most humans can be entrained to a 23.5 hour day and to a 24.65 hour day.[1]

The effect of unintended time cues is called masking. If morning rush traffic can be heard from outside, if researchers or maintenance staff appear at the same time each day, an experiment can be ruined by masking.

Free-running in humans

Non-24-hour sleep-wake syndrome, also referred to as free running disorder (FRD) or Non-24, is one of the circadian rhythm sleep disorders in humans. It affects more than half[2] of people who are totally blind (clinically known as NLP, no light perception) and a small number of sighted individuals.[3]

Among blind people, the cause is the inability to register, and therefore to entrain to, light cues. The many blind people who do entrain to the 24-hour light/dark cycle have eyes with functioning retinas including operative non-visual light-sensitive cells.[4] These ganglion cells, which contain melanopsin, convey their signals to the "circadian clock" via the retinohypothalamic tract (not the optic nerve), linking the retina to the pineal gland.[5][6]

Among sighted individuals, FRD usually first appears in the teens or early twenties. As with delayed sleep-phase disorder (DSPS or DSPD), in the absence of neurological damage due to trauma or stroke, cases almost never appear after the age of 30.[3] FRD affects many more sighted males than sighted females.[3] A quarter of sighted individuals with FRD also have an associated psychiatric condition, and a quarter of them have previously shown symptoms of DSPS.[3]

The term free-running sleep has occasionally been used by non-scientists to indicate intentional facilitation of the natural sleep/wake cycle. In this context, free-running sleep means that a person chooses to sleep when sleepy and to awaken spontaneously (specifically without an alarm clock or reference to the time of day). A decision to prioritize a natural sleep schedule over all other schedules can create conflicts with employment and social obligations.


  1. ^ Scheer, Frank A. J. L.; Kenneth P. Wright, Jr., Richard E. Kronauer, Charles A. Czeisler (2007-08-08). "Plasticity of the Intrinsic Period of the Human Circadian Timing System". PLoS ONE 2: e721. doi:10.1371/journal.pone.0000721. Retrieved 2007-12-31. "[E]xposure to moderately bright light (~450 lux; ~1.2 W/m2) for the second or first half of the scheduled wake episode is effective for entraining individuals to the 24.65-h Martian sol and a 23.5-h day length, respectively.".  
  2. ^ Teofilo Lee-Chiong (2006). Sleep: a comprehensive handbook. New York: Wiley-Liss. pp. 385. ISBN 0-471-68371-X.  
  3. ^ a b c d An American Academy of Sleep Medicine Review: Circadian Rhythm Sleep Disorders: Part II, Advanced Sleep Phase Disorder, Delayed Sleep Phase Disorder, Free-Running Disorder, and Irregular Sleep-Wake Rhythm. PDF, 18 pages. November 2007.
  4. ^ Tu DC, Zhang D, Demas J, et al. (December 2005). "Physiologic diversity and development of intrinsically photosensitive retinal ganglion cells". Neuron 48 (6): 987–99. doi:10.1016/j.neuron.2005.09.031. PMID 16364902. "Intrinsically photosensitive retinal ganglion cells (ipRGCs) mediate numerous nonvisual phenomena, including entrainment of the circadian clock to light-dark cycles, pupillary light responsiveness, and light-regulated hormone release.".  
  5. ^ Czeisler, Charles A.; Theresa L. Shanahan, Elizabeth B. Klerman, Heinz Martens, Daniel J. Brotman, Jonathan S. Emens, Torsten Klein, Joseph F. Rizzo (5 January 1995). "Suppression of melatonin secretion in some blind patients by exposure to bright light" (Full text). N Engl J Med (USA) 332 (1): 6–11. doi:10.1056/NEJM199501053320102. PMID 7990870. Retrieved 2008-02-07. "[T]he photic pathway used by the circadian system is functionally intact in some blind patients.".  
  6. ^ Arendt, Josephine (2006-02-01 [update]). "Chapter 15. The Pineal Gland and Pineal Tumours". Neuroendocrinology, Hypothalamus, and Pituitary,. pp. an E-book edited by Ashley Grossman (chapter section: Melatonin Synthesis and Metabolism). Retrieved 2008-02-07. "Image forming vision (rods and cones) is not required ... for synchronising /phase shifting the circadian clock."  

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