Temperature sensors are configured to sense a temperature for the sleeper and transmit temperature readings. A controller is configured to receive temperature readings; and send to a heating subsystem instructions to initiate a warming process that raises a distal temperature of the sleeper more than a proximal temperature of the sleeper. The heating subsystem that may include a heating element that, when engaged, can raise the distal temperature of the sleeper more than the proximal temperature of the sleeper.

A ventilator including a housing; a gas inlet port disposed in the housing and adapted to be coupled to a gas source to receive a flow of gas; a valve assembly coupled with the gas inlet port for controlling flow of gas from the gas inlet port to a gas outlet port disposed in the housing and adapted for being coupled to a patient interface to fluidly couple the gas outlet port to the airway of a patient; a controller module disposed in the housing, the controller module comprising a controller operatively coupled with the valve assembly to control operation of the valve assembly; an airway pressure sensor positioned between the valve assembly and the patient interface to measure air flow output into flowing into the airway of the patient; wherein the pressure sensor is operatively connected to the controller module to control the operation of the valve assembly in response to changes in air flow output measured by the airway pressure sensor during use.

An adaptive audio therapy system which detects and processes one or more individuals' conditions to provide adaptive, continuous audio therapy in real-time. The adaptive audio therapy system generally includes a detection device that is typically in physical contact with an individual, such as a pacifier or steering wheel. The detection device may include sensors to detect various conditions of the individual, such as heart rate, respiration rate, temperature, and the like. A computing device receives and processes the various conditions detected by the sensors. Based on the detected conditions, the computing device provides audio therapy which is adaptive to the condition of the patient and which is continuously adapted in real-time.

A method includes projecting a dark virtual sky in a digital space. The dark virtual sky is transitioned to a dawn virtual sky. The dawn virtual sky is altered to introduce a daytime virtual sky. The daytime virtual sky is modified to produce a dusk virtual sky. These operations are performed via color palette transitions in the virtual sky in a time period of less than six minutes. A collection of gaze points in the digital space includes an apex gaze point, a left descendent gaze point and a right descendent gaze point. The apex gaze point maintains a constant size, the left descendent gaze point has a first oscillation sequence that fluctuates between a minimum size, a medium size and a maximum size. The right descendent gaze point has a second oscillation sequence that fluctuates between a maximum size, a medium size and a minimum size during the time period of less than six minutes.

A method includes initiating an accelerated daily light and darkness cycle experience at a first color palette position within the accelerated daily light and darkness cycle that corresponds to a current time at a destination geographic location that a user will travel to. The accelerated daily light and darkness cycle experience is executed at a second color palette position within the accelerated daily light and darkness cycle that corresponds to the current time at the destination geographic location of the user. The accelerated daily light and darkness cycle is less than six minutes and includes projecting a dark virtual sky in a digital space, transitioning the dark virtual sky to a dawn virtual sky in the digital space, altering the dawn virtual sky to introduce a daytime virtual sky in the digital space and modifying the daytime virtual sky to produce a dusk virtual sky in the digital space.

A monitoring device (1) for a system for generating medical compressed air includes a measured air line (3) removing compressed air from a compressed air supply line downstream of a compressed air conditioning unit. A sensor (2) generates a measured signal as a function of a property of the compressed air fed through the measured air line. A humidifier (8) humidifies the compressed air upstream of the sensor. An output unit (12) outputs information about the property of the compressed air to a user on the basis of the measured signal. A tap (4) removes compressed air and an actuator (5) changes a volume flow and/or mass flow of the compressed air, which volume flow and/or mass flow prevails in the measured air line. The actuator is inserted into the tap in a measuring mode and is removed from the tap in a compressed air removal mode.

A stand-alone chamber or multi-chamber inhalation system has at least two alternative vaporized test liquid supply systems for passive or self-administered delivery of vaporized test fluid and air to one or more test chambers, which can be passive or restraint chambers, based on operator selection of delivery on and off times in a passive mode or actuation of an actuator in the chamber by a test animal in a self-administered mode. In one case, a multiple inhalation chamber system has two or more separate test fluid delivery systems and provides options for selective passive uniform drug delivery to multiple chambers or selective delivery of two or more different drugs to different groups of chambers from different delivery systems so that two different drugs or different concentrations of delivered drugs can be tested simultaneously.

A device for enclosing a positive end valve (PEEP valve) and converting the PEEP valve to an inline valve for use in a differential multi-ventilation system is described. The device includes a housing configured to enclose the PEEP valve. The housing also includes a ventilator-side arm, a pass-through arm and a patient-side arm. The pass-through arm permits extension of the multi-ventilation system to add one or more patients to the system.

A device for motion sickness reduction. The device operates by providing haptic feedback using transducers that convert electrical signals to a tactile sensation such as pressure, vibration, electrical stimulation, temperature, or airflow. The transducers are located at different locations on the body of a user, and actively change their operation to indicate a direction of motion or rotation to the user through haptic (tactile) feedback. This tactile feedback can be used to reduce motion sickness. In an embodiment, the feedback is improved by deducting motion associated with the user's visual frame of reference from motion associated with the user's vestibular frame of reference.

A stand-alone chamber or multi-chamber inhalation system has at least two alternative vaporized test liquid supply systems for passive or self-administered delivery of vaporized test fluid and air to one or more test chambers, which can be passive or restraint chambers, based on operator selection of delivery on and off times in a passive mode or actuation of an actuator in the chamber by a test animal in a self-administered mode. In one case, a multiple inhalation chamber system has two or more separate test fluid delivery systems and provides options for selective passive uniform drug delivery to multiple chambers or selective delivery of two or more different drugs to different groups of chambers from different delivery systems so that two different drugs or different concentrations of delivered drugs can be tested simultaneously.