A method for improving a physiological condition of a subject, e.g. a human or animal, is disclosed. The method comprises providing an audio signal to the subject, wherein the audio signal is associated with a virtual sound source having a shape and a position relative to the subject. The virtual sound source is defined by a plurality of virtual points, each virtual point having a position relative to the subject. The audio signal comprises audio signal components for the respective virtual points of the virtual sound source, wherein each audio signal component has been determined based on the virtual position of its associated virtual point such that the audio signal is perceived by the subject as originating from the virtual sound source having said shape and said position relative to the subject. Further, a system for performing this method is also disclosed.

A harmonic capsule may include a wooden frame that has a base portion, a wall portion both of which can support a top portion, the wall portion includes a left wall, a right wall, and a rear wall. A harmonic capsule may include alignment dowels configured to align the base portion with the wall portion and the wall portion with the top portion, and may include a plurality of fastening elements configured to removable fasten the left wall with the rear wall, the rear wall with the right wall, the base portion with the wall portion, and the top portion with the wall portion. A harmonic capsule may include at least three stabilizing feet configured to removable couple to the base portion.

A system and method for providing sensory relief from distractibility, inattention, anxiety, fatigue, and/or sensory issues to a user in need. The user can be autistic/neurodiverse, or neurotypical. The system can be configured to obtain user sensory sensitivity data indicating a user's visual, sonic, or interoceptive, sensitivities; determine, using at least the user sensory sensitivity data, sensory thresholds specific to the user and mediation data corresponding to mediations specific to the user; store the sensory thresholds and mediation data; record, using one or more sensors, a sensory input stimulus to the user; compare the sensory input stimulus with the sensory thresholds; in response to comparing the sensory input stimulus with the sensory thresholds, determine, based at least on the mediation data, a mediation to be provided to the user, the mediation configured to provide the user relief from distractibility, inattention, anxiety, fatigue, or sensory issues.

An external ventilation system of a capsule pod sleeping chamber that includes a wall with an exterior side that faces a communal space and an interior side that faces an interior of the capsule pod sleeping chamber. The external ventilation system further includes a duct to route first air out from the communal space to an area separated from air of the capsule pod sleeping chamber, where the duct is located between the exterior side and the interior side, and there is an aperture located on the exterior side opening into the duct.

A systemic human repair and enhancement system that provides stem cell therapy utilizing an apparatus and methods for administering a treatment schedule of non-invasive and drug-free narrow and specific 0.6180 Hz frequency continuous sine wave therapy to the patient's cells. The frequency therapy may be in-vivo and in-vitro applications. The frequency therapy stimulates systemic stem cell production, particularly at a tissue sites having loss of function due to a condition, aging, damage, and or disease. The frequency therapy system encompasses a narrow and specific ultra-low continuous sine wave frequency stimulation therapy that produces one or more of the enhanced cell production, release, viability, proliferation, migration and or engraftment of the human patient's own genetically compatible stem cells, and the therapy enhances the stem cell's secretions thereby safely enhancing the secretion's therapeutic effects during stem cell therapy and simultaneously systemically enhancing the patient's pre-existing cells and tissues.

A pain management system and methodology for preventing or alleviating chronic pain, and/or pain associated with a medical procedure prior to the medical procedure being performed, includes (a) aurally isolating a patient for a chosen period shortly prior to the patient receiving propofol in accordance with step (c), (b) exposing the patient to a repetitive, positive message during the chosen period, and (c) subsequently administering an effective quantity of propofol to the patient. For step (b), the repetitive, positive message may be delivered from a pre-recorded memory card inserted in headphones.

Environmental characteristics or scenes of habitable environments (e.g., hotel or motel rooms, spas, resorts, cruise boat cabins, offices, hospitals and/or homes, apartments or residences, or other spaces or sub-spaces) are controlled to facilitate certain activities of a user in the environment by increasing focus, preparing for sleep, directing movement, masking ambient noise, and improving air quality, among others. Controllable characteristics include, for example, lighting, CO.sub.2/O.sub.2 levels, humidity levels, sound, aroma, and air temperature. Controls are provided for the occupant and/or facility personnel to select activities or scenes, or sensors detect the activity and implement an appropriate scene.

A self-contained, hyperthermic conditioning unit and selectively controllable environment for exercising. The unit comprises a base portion having a bed therein and a removable cover connected to the base portion to enclose a personal compartment within the unit. One or more heating elements provide heat to the personal compartment and one more pieces of physical exercise equipment are provided within the personal compartment.

The invention relates to a device for olfactory stimulation of a patient with a plurality of scents, said device comprising: —a source (2) of a carrier gas (G); —a plurality of scent odorization circuits, each odorization circuit (4) comprising: —a container (18) containing an odorous volatile substance (V), —a container inlet line (26), provided with a container inlet valve (28), connecting an inlet (30) of said container with said source of carrier gas, and —a container outlet line (36), provided with a container outlet valve (38), connecting an outlet (40) of said container with an exit line (12); —a control unit (8), configured to control said container inlet valve and container outlet valve according to a medical protocol.

The present technology relates to a light-shielding device and a light-shielding method which make an object that is meant to be invisible to human beings enter a state in which the object is hidden so as to be invisible to eyes, or make an object that is meant to be visible enter a state in which the object is visible to eyes in correspondence with biological information. A light-shielding wall, which partitions two spaces and includes a plurality of panels capable of being controlled to a transmitting state in which light is transmitted or a light-shielding state in which light is shielded, is used as a window, an orientation of a face of a user who is sleeping is detected as biological information, and the light-shielding wall is controlled so that the user is capable of visually recognizing light when it reaches an alarm setting time.