The device is in the field of sensory experience mechanisms, and more specifically, sensory and experiential enhancement mechanisms that can be positioned within a patient care or hospice setting for providing sensory-based therapy to patients.
Within hospitals and other care settings, it is typical that a television screen is provided for visual stimulation. Items that the patient happens to bring with them also provide visual stimulation. With certain conditions such as dementia and Alzheimer's disease, this television provides a limited amount of visual and auditory stimulation through this single interface.
According to one aspect of the present device, a patient experience interface includes at least one display. An experience frame is positioned proximate the display. A sensory interface is positioned within the experience frame and includes a plurality of sensory stimulation devices. One of the sensory stimulation devices is a sunlight simulation device that operates independently or in conjunction with another of the sensory stimulation devices of the plurality of sensory stimulation devices. The plurality of sensory stimulation devices operate through a sequence of activations to stimulate various senses of a patient.
According to another aspect, a movement assist chair for use in a patient space includes a chair frame having a back and a plurality of legs. A seating module is attached to the chair frame and includes an upper seat cushion. A resilient internal platform is positioned within the seating module and below the upper seat cushion. The resilient internal platform is biased to a resting position. Upon a patient resting upon the resilient internal platform, the resilient internal platform deflects in a downward direction toward a seating position that is below the resting position and contemporaneously exerts an upward biasing force that assists the patient in reaching a seated position and also assists the patient is moving upward from the seated position to exit the seating module.
According to another aspect, a seating module for use with a chair frame includes a perimeter frame member. A resilient internal platform is attached to the perimeter frame member at a static portion. An upper seat cushion is disposed on top of a resilient internal platform. The resilient internal platform is biased to an original shape that defines a resting position. Upon a patient resting upon the resilient internal platform, the resilient internal platform deflects in a downward direction toward a seating position and contemporaneously exerts an upward biasing force that assists the patient in reaching a seated position and also assists the patient is moving upward from the seated position.
These and other aspects, objects, and features of the present disclosure will be understood and appreciated by those skilled in the art upon studying the following specification, claims, and appended drawings.
In the drawings:
As required, detailed embodiments of the present disclosure are disclosed herein; however, it is to be understood that the disclosed embodiments are merely exemplary of the invention that may be embodied in various and alternative forms. The figures are not necessarily to a detailed design; some schematics may be exaggerated or minimized to show function overview. Therefore, specific structural and functional details disclosed herein are not to be interpreted as limiting, but merely as a representative basis for teaching one skilled in the art to variously employ the present invention.
For purposes of description herein, the terms “upper,” “lower,” “right,” “left,” “rear,” “front,” “vertical,” “horizontal,” and derivatives thereof shall relate to the concepts as oriented in
The present illustrated embodiments reside primarily in combinations of method steps and apparatus components related to a patient experience interface that operates to stimulate the patient through a range of sensory experiences that operate within and around the patient space. Accordingly, the apparatus components and method steps have been represented, where appropriate, by conventional symbols in the drawings, showing only those specific details that are pertinent to understanding the embodiments of the present disclosure so as not to obscure the disclosure with details that will be readily apparent to those of ordinary skill in the art having the benefit of the description herein. Further, like numerals in the description and drawings represent like elements.
As used herein, the term “and/or,” when used in a list of two or more items, means that any one of the listed items can be employed by itself, or any combination of two or more of the listed items, can be employed. For example, if a composition is described as containing components A, B, and/or C, the composition can contain A alone; B alone; C alone; A and B in combination; A and C in combination; B and C in combination; or A, B, and C in combination.
In this document, relational terms, such as first and second, top and bottom, and the like, are used solely to distinguish one entity or action from another entity or action, without necessarily requiring or implying any actual such relationship or order between such entities or actions. The terms “comprises,” “comprising,” or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a process, method, article, or apparatus that comprises a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus. An element proceeded by “comprises . . . a” does not, without more constraints, preclude the existence of additional identical elements in the process, method, article, or apparatus that comprises the element.
As used herein, the term “about” means that amounts, sizes, formulations, parameters, and other quantities and characteristics are not and need not be exact, but may be approximate and/or larger or smaller, as desired, reflecting tolerances, conversion factors, rounding off, measurement error and the like, and other factors known to those of skill in the art. When the term “about” is used in describing a value or an end-point of a range, the disclosure should be understood to include the specific value or end-point referred to. Whether or not a numerical value or end-point of a range in the specification recites “about,” the numerical value or end-point of a range is intended to include two embodiments: one modified by “about,” and one not modified by “about.” It will be further understood that the end-points of each of the ranges are significant both in relation to the other end-point, and independently of the other end-point.
The terms “substantial,” “substantially,” and variations thereof as used herein are intended to note that a described feature is equal or approximately equal to a value or description. For example, a “substantially planar” surface is intended to denote a surface that is planar or approximately planar. Moreover, “substantially” is intended to denote that two values are equal or approximately equal. In some embodiments, “substantially” may denote values within about 10% of each other, such as within about 5% of each other, or within about 2% of each other.
As used herein the terms “the,” “a,” or “an,” mean “at least one,” and should not be limited to “only one” unless explicitly indicated to the contrary. Thus, for example, reference to “a component” includes embodiments having two or more such components unless the context clearly indicates otherwise.
Referring to
The term “patient” is used generically within this specification and is meant to refer to the individual that receives the sensory stimulation. It can refer to individuals that are admitted, under the care of another, living independently, and other similar situations and ranges of care. In this regard, the patient space 20 is the area surrounding the patient, wherever they may be located. In this manner, the term patient space 20 can refer to any one of various institutional settings or residential settings. The patient space 20 can also refer to indoor and outdoor spaces depending on the location and surrounding environment of the patient.
By way of example, and not limitation, the various sensory experiences can include, but are not limited to, lighting 30, air handling components 32, auditory components 34, fragrancing mechanisms 36, haptic and tactile interfaces 38, and other similar sensory experiences.
The lighting 30 can be in the form of a traditional lighting element or can be in the form of a variable lighting array 68 or combination of lighting elements that can be operated in any one or more illuminated and deluminated configurations. The lighting 30 can also be in the form of a sunlight simulation device 64. The sunlight simulation device 64 utilizes specific lighting elements that give off wavelengths of light that mimic a myriad of sunlight experiences. By mimicking sunlight, the sunlight simulation device 64 encourages the patient's brain to reduce the production of melatonin (a hormone that makes you sleepy) and increase the production of serotonin (a hormone that affects mood). The lighting elements incorporated into the sunlight simulation device 64 can be in the form of various wavelengths that produce various colors of light, color temperatures, hues, intensities of lights, various levels of UV light or UVB light and other lighting configurations. The sunlight simulation device 64 can operate independently or can operate in conjunction with any one or more of the other sensory stimulation devices 66. As discussed herein, these sensory stimulation devices 66 can include, but are not limited to the display 60, auditory components 34, air handling components 32, fragrancing mechanisms 36, tactile interfaces 38 and other aspects of the sensory interface 10 of the patient experience interface.
The sunlight simulation device 64 and the other sensory stimulation devices 66 can be activated and deactivated in any one of various sequences of activations. These sequences of activations can be predetermined to mimic specific experiential conditions, such as a sunny day in a park, or sitting on a beach. The sequence of activations an also be randomized to interface with the senses of the patient in an unpredictable way or a way that the patient must attempt to decipher and/or articulate. The various sequences of activations typically include simultaneous, contemporaneous, or overlapping operation of at least two of the sensory stimulation devices 66. The various sequences of activations can also be activated and deactivated based upon various external factors. Such factors can include, but are not limited to, time of day, outside temperature, weather, and other similar external factors. The sequences of activations can also be activated based upon internal factors related to the patient. Such internal factors can include, but are not limited to, heart rate, breathing rate, amount of movement by a patient over time, the type of movement being undertaken by a patient, and other similar factors.
Referring again to
Referring again to
It is contemplated that the various sensory stimulation devices 66 can be used sequentially, in combination, cooperatively and in other various permutations and configurations to stimulate a single sense of the patient, but more typically, multiple senses, and combinations of senses, of the patient at the same time or in a variety of sequences and patterns.
According to various aspects of the device, the sensory therapy device 12 can utilize the various sensory stimulation devices 66 to provide heightened experiences to one sense, or a specific combination of senses, of the patient while diminishing the stimulation of other senses. Subsequently, a different sense or combination of senses of the patient can be heightened while stimulation of the other senses can be diminished. A goal of the sensory therapy device 12 is to provide a variable, and typically non-repeating, interaction of various sensory components using the sensory therapy device 12. Accordingly, the therapy device 12 can isolate specific senses of the patient to produce heightened experiences among each of the patient's senses over time.
The sensory therapy device 12 can be wirelessly controlled, controlled through a remote within the room, pre-programmed, combinations thereof, or otherwise operated by various controllers for manipulating the configuration of the sensory stimulation devices 66 of the sensory therapy device 12. The sensory therapy device 12 can also be programmed to respond to certain movements of the patient. In such an aspect of the device, where the patient performs a repeated activity, the sensory therapy device 12 can modify the sensory experience during each successive occurrence of the repeated activity. Though this configuration, a repeated activity can be a unique experience during each successive occurrence. These changes over time can be subtle or profound to activate different sensory perceptions of the patient in a variety of ways.
As exemplified in
It is contemplated that various haptic and tactile features can be positioned near the patient's bed 50 or at positions within the patient space 20. In such an embodiment, the sensory therapy device 12 can activate various tactile and other sensory components throughout the patient space 20, according to the random or predefined sequence. It is also contemplated that the sensory therapy device 12 can include at least one display 60 and can also include multiple displays 60 throughout the room for providing a range of sensory information to the patient throughout the course of the day and over extended periods of time. These secondary displays 60 can be positioned on windows, ceilings, furniture, walls, floors 226, or other surfaces within the patient space 20.
By way of example, and not limitation, the sensory therapy device 12 can include a plurality of screens or surfaces that can be made from LED devices or other similar flat panel displays 60. These flat panel displays 60 can be coordinated to cooperatively provide varying sensory interactions to the patient. Various mobile displays 60 can be also be utilized where the patient moves and the patient space 20 moves along with the patient. In this manner, the patient can take portions of the sensory device and the sensory stimulation devices 66 to appointments and other locations, such as portions of the hospital, healthcare facility or living space, or outside of the facility. Through the sensory therapy device 12, the system of sensory interactions can provide a consistent sensory interactive experience that can be used to stimulate the senses of the patient through various settings and conditions. This consistent sensory interactive experience can also be portable to move with the patient and the surrounding patient space 20.
Referring now to
It is also contemplated that the storage organizer 70 can include a catalog system that assists the patient, the patient's family, visitors and healthcare staff to identify the locations of items that are stored therein. The catalog system can include a list of items, various graphic indicia, photographs, digital tags, combinations thereof and other informational graphics to identify the proper location or placement of the patient's items, as discussed above.
The positioning of the storage organizer 70 provides placement for personal and significant items so that the room can be used for promoting identity and sense of place to the patient. By promoting routine and enhancing the sense of place and identity for the patient, therapies for dementia and Alzheimer's patients can be enhanced and supported throughout the day, and not just when formal therapies are occurring.
Referring now to
The charging station 96 can include a tabletop 110 that can extend over a portion of the patient's bed 50 for providing a convenient task area for the patient. This task area can include one or more electrical outlets 112, USB ports, or other electrical interfaces that can be used with the patient's devices. The base 92 of the mobile device 90 can include a footrest and lockable wheels 224 for comfort and convenience. A mobile WiFi hotspot can be included within the mobile device 90 for maintaining connectivity with the patient's devices. Certain portions of the mobile device 90 can include storage pockets, storage cubicles and other storage apertures 114 for containing prescriptions, medical records and information, personal care items, task-related items, items of personal significance, and other items that may be closely related to the task space and mobile devices 90 owned and used by the patient. The mobile device 90 can also include one or more displays 60 that are integrated with the other components of the sensory therapy device 12.
According to the various aspects of the device, the charging station 96 and the mobile device 90 are configured to have a generally mating configuration. In this manner, the shape of the tabletop 110 of the mobile device 90 typically includes a profile that cooperatively engages with the profile of the charging station 96. Accordingly, the tabletop 110 and other horizontal surfaces of the mobile device 90 can include a rounded configuration, angular configuration or other shape, and the profile of the charging station 96 will include a respective profile to receive the mobile device 90 for charging and storage, as shown in an exemplary and non-limiting fashion in
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As exemplified in
According to the various aspects of the device, the resilient internal platform 242 as well as the magnitude of the biasing force 246 can be modified or calibrated to provide a sufficient biasing force 246 for users having a height and weight that can vary across a wide range of demographics. These adjustments can be made by changing the thickness of the material of the resilient internal platform 242 or by adding various springs or other resilient members or biasing members.
Referring again to
It is to be understood that variations and modifications can be made on the aforementioned structure without departing from the concepts of the present invention, and further it is to be understood that such concepts are intended to be covered by the following claims unless these claims by their language expressly state otherwise.
This application claims priority to and the benefit under 35 U.S.C. § 119(e) of U.S. Provisional Patent Application No. 63/231,841 filed on Aug. 11, 2021, entitled SENSORY AND EXPERIENTIAL ENHANCEMENTS FOR A HOSPITAL SETTING, and U.S. Provisional Patent Application No. 63/351,622 filed on Jun. 13, 2022, entitled SENSORY AND EXPERIENTIAL ENHANCEMENTS FOR PATIENT CARE SETTINGS WITHIN HOME AND HOSPITAL ENVIRONMENTS, the entire disclosures of which are hereby incorporated herein by reference.
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