Systems and methods of treating medical conditions using arrays of planar coils configured to generate pulsed electromagnetic fields and integrated into clothing
11517760 · 2022-12-06
Inventors
Cpc classification
G06K19/027
PHYSICS
International classification
A61N2/02
HUMAN NECESSITIES
Abstract
The present specification discloses a pulsed electromagnetic field system having planar microcoil arrays integrated into clothing. Each of the planar microcoil arrays has two or more planar microcoils positioned on a flexible substrate. The planar microcoil arrays are connected to a controller configured to generate an electrical current and transmit that electrical current, in accordance with a particular stimulation protocol, to each of the planar microcoil arrays.
Claims
1. A pulsed electromagnetic field device comprising: an article of clothing; a controller; and a plurality of planar microcoil arrays, wherein each of the plurality of planar microcoil arrays comprises a flexible substrate and two or more planar microcoils embedded in the flexible substrate, wherein each of the two or more planar microcoils is defined by a conductive pathway embedded within the flexible substrate, wherein a first of the plurality of planar microcoil arrays is physically spaced apart from, and non-contiguous with, a a second of the plurality of planar microcoil arrays, wherein each of the plurality of planar microcoil arrays is integrated into the article of clothing; and wherein each of the plurality of planar microcoil arrays is in electrical communication with the controller such that the first of the plurality of planar microcoil arrays and the second of the plurality of planar microcoil arrays are electrically coupled to the controller in parallel.
2. The pulsed electromagnetic field device of claim 1, further comprising a docking station, wherein the docking station is configured to releasably receive the controller.
3. The pulsed electromagnetic field device of claim 2, wherein the docking station comprises a first mechanical connector and a first electrical interface, wherein the controller comprises a second mechanical connector and a second electrical interface, and wherein, upon the first mechanical connector and the second mechanical connector latching, the first electrical interface is automatically placed in electrical communication with the second electrical interface.
4. The pulsed electromagnetic field device of claim 1, wherein the article of clothing comprises two or more layers of material and wherein the plurality of planar microcoil arrays is positioned between the two or more layers of material.
5. The pulsed electromagnetic field device of claim 1, wherein the article of clothing is a sock, a shoe, a shirt, a pant, a glove, a mask, a neck covering, a head covering, a headband, a sleeve, or a brace configured to fit over an elbow, an ankle, or a knee.
6. The pulsed electromagnetic field device of claim 1, wherein the controller is configured to generate a pulse train, wherein each pulse train comprises a plurality of pulses having an amplitude in a range of 1 mA to 200 mA.
7. The pulsed electromagnetic field device of claim 6, wherein the pulse train comprises a first pulse having a first amplitude, a second pulse having a second amplitude, and a third pulse having a third amplitude, wherein the first amplitude is less than the second amplitude and the second amplitude is less than the third amplitude.
8. The pulsed electromagnetic field device of claim 7, wherein each of the first pulse, second pulse, and third pulse has a square shape.
9. The pulsed electromagnetic field device of claim 6, wherein each of the two or more planar microcoils is configured to generate a magnetic field in a range of 3 microTesla to 500 microTesla upon receiving the pulse train.
10. The pulsed electromagnetic field device of claim 1, wherein each of the plurality of planar microcoil arrays comprises at least six planar microcoils.
11. The pulsed electromagnetic field device of claim 10, wherein each of the plurality of planar microcoil arrays comprises an input terminal configured to receive current from the controller, an output terminal, and at least two traces to electrically connect each of the at least six planar microcoils to the input terminal and the output terminal.
12. The pulsed electromagnetic field device of claim 11, wherein a first set of the at least six planar microcoils is configured to direct current clockwise and wherein a second set of the at least six planar microcoils is configured to direct current counterclockwise.
13. The pulsed electromagnetic field device of claim 11, wherein the input terminal, output terminal, and at least two traces are each embedded into the flexible substrate.
14. The pulsed electromagnetic field device of claim 12, wherein a number of coils in the first set of the at least six planar microcoils is equal to a number of coils in the second set of the at least six planar microcoils.
15. The pulsed electromagnetic field device of claim 11, wherein all of the at least six planar microcoils are configured to direct current in a same direction.
16. The pulsed electromagnetic field device of claim 1, wherein each of the two or more planar microcoils is at least one of a spiral circular planar microcoil, a rectangular circular planar microcoil, a non-spiral circular planar microcoil, or a non-spiral rectangular planar microcoil.
17. The pulsed electromagnetic field device of claim 1, wherein a first subset of the plurality of planar microcoil arrays has a different surface area than a second subset of the plurality of planar microcoil arrays.
18. The pulsed electromagnetic field device of claim 1, wherein each of the plurality of planar microcoil arrays has a same surface area.
19. The pulsed electromagnetic field device of claim 1, wherein the controller is configured to generate a time varying current in order to create a time varying magnetic field at each of the plurality of planar microcoil arrays.
20. The pulsed electromagnetic field device of claim 19, wherein the time varying current is defined by square waves having substantially equal peak amplitude values.
21. The pulsed electromagnetic field device of claim 19, wherein the time varying current is defined by sinusoidal waves having substantially equal peak amplitude values.
22. The pulsed electromagnetic field device of claim 19, wherein the time varying current is defined by square waves having substantially different peak amplitude values.
23. The pulsed electromagnetic field device of claim 19, wherein the time varying current is defined by a train of square waves and wherein, in each train, the square waves have peak values that ramp from a low peak amplitude value to a higher peak amplitude value.
24. The pulsed electromagnetic field device of claim 1, wherein the controller is configured to cause an electrical current to be concurrently transmitted to all of the plurality of planar microcoil arrays.
25. The pulsed electromagnetic field device of claim 1, wherein the controller is configured to cause an electrical current to be transmitted to all of the plurality of planar microcoil arrays at different times.
26. The pulsed electromagnetic field device of claim 1, further comprising a set of programmatic instructions stored on a separate computing device, wherein, when executed by the separate computing device, the programmatic instructions generate a display for prompting a user to input a pain level and a locus of pain.
27. The pulsed electromagnetic field device of claim 26, wherein, when executed by the separate computing device, the programmatic instructions determine which of the plurality of planar microcoil arrays should receive an electrical current based on at least one of the pain level or the locus of pain.
28. The pulsed electromagnetic field device of claim 26, wherein, when executed by the separate computing device, the programmatic instructions generate data indicative of which of the plurality of planar microcoil arrays should receive an electrical current based on at least one of the pain level or the locus of pain and transmit the data to the controller.
29. The pulsed electromagnetic field device of claim 28, wherein the controller generates an electrical current based on the data and in a predefined pattern based on at least one of the pain level or the locus of pain.
30. The pulsed electromagnetic field device of claim 1, further comprising a plurality of traces integrated into the article of clothing and extending from each of the plurality of planar microcoil arrays to the controller.
31. A method of treating a condition, comprising: forming an article of clothing adapted to be attached to a portion of a patient's body, wherein the article of clothing comprises a plurality of planar microcoil arrays, wherein each of the plurality of planar microcoil arrays comprises a flexible substrate and two or more planar microcoils embedded in the flexible substrate, wherein each of the two or more planar microcoils is defined by a conductive pathway embedded within the flexible substrate, wherein a first of the plurality of planar microcoil arrays is physically spaced apart from and non-contiguous with a second of the plurality of planar microcoil arrays, wherein each of the plurality of planar microcoil arrays is integrated into the article of clothing; and wherein each of the plurality of planar microcoil arrays is in electrical communication with a connector integrated into the article of clothing; attaching a controller to the connector, wherein the controller comprises a circuit and a power source; and activating the controller to cause a time varying current to be transmitted to each of the plurality of planar microcoil arrays such that the first of the plurality of planar microcoil arrays and the second of the plurality of planar microcoil arrays are electrically coupled to the controller in parallel.
32. The method of claim 31, wherein the condition is at least one of an anxiety disorder, an obsessive compulsive disorder, pain, a post-traumatic stress disorder, memory degeneration, schizophrenia, Parkinson's disease, stroke rehabilitation, drug addiction, drug cravings, depression, depression-related conditions, post-partum depression, bipolar depression, auditory hallucinations, multiple sclerosis, fibromyalgia, Alzheimer's disease, spinocerebellar degeneration, epilepsy, urinary incontinence, movement disorders, chronic tinnitus, or sleep apnea.
33. The method of claim 31, further comprising attaching the article of clothing such that at least one of the two or more planar microcoils in at least one of the plurality of planar microcoil arrays is positioned over an acupoint of the patient's body.
34. The method of claim 31, wherein, upon attaching the controller to the connector, the circuit automatically electrically interfaces with at least one of the plurality of planar microcoil arrays.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) These and other features and advantages of the present specification will be further appreciated, as they become better understood by reference to the following detailed description when considered in connection with the accompanying drawings:
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DETAILED DESCRIPTION
(44) The present specification is directed towards multiple embodiments. The following disclosure is provided in order to enable a person having ordinary skill in the art to practice the invention. Language used in this specification should not be interpreted as a general disavowal of any one specific embodiment or used to limit the claims beyond the meaning of the terms used therein. The general principles defined herein may be applied to other embodiments and applications without departing from the spirit and scope of the invention. Also, the terminology and phraseology used is for the purpose of describing exemplary embodiments and should not be considered limiting. Thus, the present invention is to be accorded the widest scope encompassing numerous alternatives, modifications and equivalents consistent with the principles and features disclosed. For purpose of clarity, details relating to technical material that is known in the technical fields related to the invention have not been described in detail so as not to unnecessarily obscure the present invention.
(45) In the description and claims of the application, each of the words “comprise” “include” and “have”, and forms thereof, are not necessarily limited to members in a list with which the words may be associated. It should be noted herein that any feature or component described in association with a specific embodiment may be used and implemented with any other embodiment unless clearly indicated otherwise.
(46) As used herein, the indefinite articles “a” and “an” mean “at least one” or “one or more” unless the context clearly dictates otherwise.
(47) As used herein, the term “planar coil” or “planar microcoil” both refer to a conductive pathway with curves or turns where the entirety of the conductive pathway is substantially positioned within the same plane. Stated differently, the turns, curves, or coils of the conductive pathway occupy varied positions within an X-Y plane but are of the same thickness or have a thickness within a range of 20% of each other. Accordingly, such a planar microcoil is differentiated from conventional coil structures because the windings or turns of the coil do not extend substantially upward or outward from the innermost or first coil in the Z direction or normal to the X-Y plane defined by the innermost or first coil. The terms “extend substantially upward or outward”, “within the same plane”, or “within the same X-Y plane” are defined as within +/−20 mm, within +/−15 mm, within +/−10 mm, or more preferably within +/−5 mm of a 0 point on the Z axis. The planar footprint area of a “planar coil” or “planar microcoil” is preferably greater than 1 cm.sup.2, more preferably between 1 cm.sup.2 and 9 cm.sup.2, and even more preferably between 2 cm.sup.2 and 4 cm.sup.2.
(48) As used herein, the term “magnetic flux” refers to a quantity or strength of magnetic lines produced by a current passing through one or more planar coils and the term “magnetic flux density” refers to the amount of that magnetic flux in an area taken perpendicular to the magnetic flux's direction, typically measured in Tesla. It should be appreciated that, throughout this specification and in each embodiment taught here, all magnetic fields, and corresponding magnetic flux and magnetic flux densities, are generated by a current passing through one or more planar coils and are not generated by one or more permanent magnets unless otherwise stated. It should further be appreciated that each embodiment described herein may further include an optional version which expressly does not include, incorporate, or otherwise use permanent magnets but, yet, which still generate magnetic fields.
(49) Planar Microcoil Structure
(50) Referring to
(51) Similarly,
(52) It should be appreciated that the present invention is directed toward any spiral shaped planar microcoil, including polygonal, elliptical, or other shapes, having a plurality of turns where the conductive pathway follows a spiral shape from a first part of the circuit, or where the spiral coil conductive pathway begins, to a second part of the circuit, or where the spiral coil conductive pathway terminates. In such embodiments, each turn would form the same polygonal, elliptical, or other shape, except that the beginning and end of the shape are offset from each other, thereby creating a spiral across all turns. The spiral shaped conductive pathway would also be substantially entirely positioned within the same X-Y plane.
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(54) Similarly,
(55) It should be appreciated that the present invention is directed toward any non-spiral shaped planar microcoil, including polygonal, elliptical, or other shapes, having a plurality of turns where the conductive pathway follows a polygonal, elliptical, or other shape from a first part of the circuit, or where the coil conductive pathway begins, to a second part of the circuit, or where the coil conductive pathway terminates. In such embodiments, each turn would form the same incomplete polygonal, elliptical, or other shape and would share a common electrical input and electrical output with the adjacent turns, thereby creating a set of nested incomplete polygonal, elliptical, or other shapes, each in electrical communication with a common electrical input and electrical output and each having a progressively smaller (or larger) length and width or radius. The conductive pathway of nested incomplete polygonal, elliptical, or other shapes would be substantially entirely positioned within the same X-Y plane
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(58) Table 1 has a list of preferred attributes of each of the spiral circular coil (
(59) TABLE-US-00001 TABLE 1 Coil Attributes Spiral Spiral Non-spiral Non-spiral circular coil rectangular coil circular coil rectangular coil Variables FIG. 1a FIG. 1b FIG. 2a FIG. 2b Width of the coil 1 to 200 microns 1 to 200 microns 1 to 200 microns 1 to 200 microns segments (note that (preferably 25 to (preferably 25 (preferably 25 to (preferably 25 to 100 the widths may be 100 microns, to 100 microns, 100 microns, microns, preferably constant or preferably 50 preferably 50 preferably 50 50 microns) variable) microns) microns) microns) Distance from 10 to 500 10 to 500 10 to 500 microns 10 to 500 microns center of coil to microns microns (preferably 100 (preferably 100 innermost coil (preferably 100 (preferably 100 microns) microns) segment microns) microns) Distance from 43 to 800250 43 to 800250 43 to 800250 43 to 800250 center to the microns, where microns, where microns, where microns, where the outermost coil the max distance the max the max distance max distance is segment is calculated distance is is calculated calculated using 100 using 100 calculated using using 100 microns for the width microns for the 100 microns for microns for the of the coil segment, width of the coil the width of the width of the coil 250 microns for the segment, 250 coil segment, segment, 250 distance from the microns for the 250 microns for microns for the center of the coil to distance from the the distance distance from the the innermost coil center of the coil from the center center of the coil segment, pitch is to the innermost of the coil to the to the innermost 1500 microns, coil segment, innermost coil coil segment, number of turns is pitch is 1500 segment, pitch pitch is 1500 500 microns, number is 1500 microns, number of turns is 500 microns, of turns is 500 number of turns is 500 Distance between 10 to 3000 10 to 3000 10 to 3000 10 to 3000 microns each coil segment, microns microns microns (preferably 50, 200, referred to as pitch (preferably 50, (preferably 50, (preferably 50, 650, 1150 microns) (note that the pitch 200, 650, 1150 200, 650, 1150 200, 650, 1150 may be constant or microns) microns) microns) variable) Height of the coil 0.1 to 20 0.1 to 20 0.1 to 20 microns 0.1 to 20 microns segments microns microns (preferably 1 (preferably 1 micron) (preferably 1 (preferably 1 micron) micron) micron) Number of turns 3 to 500 3 to 500 3 to 500 3 to 500 (preferably (defined as the (preferably 5, 20, (preferably 5, (preferably 5, 20, 5, 20, 48, 94) number of times a 48, 94) 20, 48, 94) 48, 94) coil travels around the center of the coil at least 270 degrees) Support structure SiO.sub.2/Si, wafer, SiO.sub.2/Si, wafer, SiO.sub.2/Si, wafer, SiO.sub.2/Si, wafer, Kapton, flexible Kapton, flexible Kapton, flexible Kapton, flexible
(60) Referring back to
(61) 1. The coil, including any hard-plastic backing, has a footprint no greater than 2 cm by 2 cm, preferably no greater than 1.65 by 1.65 centimeters.
(62) 2. The coil comprises a plurality of wire turns, where the diameter of the coil in the plane of the coil is 0.04 mm.
(63) 3. The coil will have a minimum of 100 turns, preferably 175 windings, and even more preferably greater than 150 windings.
(64) 4. Each corner of the coil will have 1 quarter-circle with a radius of 0.18125 cm.
(65) 5. The inductance is in a range of 200 to 700 uH, preferably around 373 uH and the resistance is in a range of 50 to 800 ohms, preferably around 144 ohms.
(66) 6. The inner air core has dimensions in a range of 0.2 cm by 0.2 cm with each corner of the inner air core being 1 quarter-circle with a radius of 0.00625 cm.
(67) Planar Microcoil Arrays and Controllers
(68) Referring to
(69) In one embodiment, the single patch 620 comprises two or more planar microcoils 615 or between 2 and 100 microcoils or more than 2 planar microcoils. In one embodiment, the set of patches used in any specific application, including in any piece of clothing, may have different sizes (e.g. surface areas), and therefore different numbers of planar microcoils, in order to better fit or suit different parts of a person's anatomy. For example, clothing positioned adjacent to the patient's torso may have larger patches, and more planar microcoils, integrated into a single patch than clothing positioned near the patient's toes or fingers, which may have smaller patches to better contour to the curves and crevices near the patient's toes or fingers, as further discussed in relation to
(70) Controller 605 may be programmed to concurrently stimulate all the planar microcoils in all the patches, all planar microcoils on a subset of the patches, or a subset of planar microcoils on a subset of the patches. Further, the controller 605 may be optionally configured to removably interface with a docking station 675. Referring to
(71) In one embodiment, programmatic instructions on a separate computing device, such as a phone, 635, are executed to capture pain data from the patient, analyze the pain data to determine which areas of the patient's anatomy requires pulsed electromagnetic field therapy, and, depending on the garment being worn by the patient, activate one or more planar microcoils on one or more patches to target the determined areas requiring pulsed electromagnetic field therapy.
(72) More specifically, referring to
(73) After receiving the user's response to the clearance questions, the app determines if there are any contraindications to use (i.e. a pacemaker, spinal implants, pins, or other implanted devices) 1310 and, depending upon the determination, generates an activation code which is transmitted to the controller 605. If the user inputted data is contraindicated for use with the specific piece of clothing, the app recommends the user first activate the device under the supervision of a physician. An override code, which would require the user to actively acknowledge the risks involved, may be provided by the app and either wirelessly transmitted to the controller 605 or displayed to the user who may manually input it into the controller 605.
(74) If user, relative to the identified piece of clothing, is cleared for use and the controller 605 is activated, the app then prompts the user to input data indicative of the patient's pain level and location of the pain 1315. The app may do so by generating a visual analog scale that the user may use to indicate a level of pain being experienced (i.e. on a scale of 1 to 10 or using graphical emojis) and a graphical image of a human body, or portions thereof, to allow the user to identify, by pointing to the right location on the graphical image, the locus of pain. In one embodiment, the graphical image used is specific to the type of clothing identified using the original code indicative of the clothing acquired. Once the degree and/or locus of pain has been identified, the app may determine which set of patches and/or set of planar microcoils should be energized in order to treat the inputted level and location of pain 1320 and transmit such data to the controller. For other conditions, other questions may be posed, such as degree and timing of memory lapses, degree and timing of tremors, or degree and timing of other symptoms.
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(76) Referring to
(77) Similarly, the output lead of each coil 1508 may be routed to one side of the array 1514 and may be kept separate from each other by one or more layers of insulation tape 1512. The output leads of all the coils 1508 of the array 1500 are integrated or multiplexed together to form an output terminal 1524 to which electrical current from the controller and energy source may be directed. Accordingly, the output leads of all the coils 1508 of the array 1500 are integrated or multiplexed together to form an output terminal 1524 to which electrical current may be directed from the array to the controller and energy source. Further, all the coils 1508 of the array 1500 may form a closed circuit by directing current from the array to the single energy or battery source via the one output terminal 1524.
(78) Preferably, positioned between each coil piece 1504 or coil 1508 is a material that may act as a cushion, barrier, or padding 1518 that functions to both prevent the coil pieces from 1504 shifting and to gently position the array 1500 against the user's skin. Additionally, or alternatively, area 1518 may include an adhesive to attach, secure, or otherwise fixedly position the array 1500 against the user's skin. Additionally, or alternatively, area 1518 may include an attachment mechanism, such as Velcro or snaps, to attach area 1518, and therefore array 1500, to another substrate or material to form a piece of clothing, as further discussed below.
(79) It should be appreciated that the directionality of the current of each coil may be modified to achieve a desired magnetic flux level by properly routing its input lead or output lead to the input or output side of the array 1500. Referring to
(80) It should further be appreciated that the form factor and range of coil sizes and relative separation between coil pieces are important to achieving two core objectives. First, the coil footprint should not be too large, and the coil separation should not be too small, otherwise the array will not be flexible enough to conform to uneven or non-planar portions of a user's body. Second, the coil footprint should not be too small, and the coil separation should not be too large, otherwise the array will not generate a sufficiently large magnetic flux for therapeutic purposes. Hence, the dimensions and distances disclosed herein have a distinct utility and are not merely aesthetic in nature.
(81) Stimulation Protocols
(82) The controller is configured to generate an electrical current, and selectively transmit the electrical current to all of the plurality of planar microcoils, or a subset of the plurality of planar microcoils, in order to generate pulsed electromagnetic fields in accordance with one or more of
(83) A stimulation session may go from 1 minute to 24 hours. As described above, within a given stimulations session, you may have a series of pulse bursts. A pulse burst may have one or more pulses. Each pulse in the pulse burst may have the same or different pulse shapes, as shown in
(84) TABLE-US-00002 TABLE 2 Pulse Burst Characteristics Amplitude of 1 mAmp to 1 Amp 1 mAmp to 1 Amp 1 mAmp to 1 Amp 1 mAmp to 1 Amp electrical signal (preferably 0.1, (preferably 0.1, (preferably 0.1, (preferably 0.1, generated by the 0.2, 0.4 0.5, 0.2, 0.4 0.5, 0.2, 0.4 0.5, 0.2, 0.4 0.5, controller 0.55 Amps) 0.55 Amps) 0.55 Amps) 0.55 Amps) Frequency of 1 Hz to 500 Hz 1 Hz to 500 Hz 1 Hz to 500 Hz 1 Hz to 500 Hz electrical pulse (preferably 5 to (preferably 5 to (preferably 5 to (preferably 5 to bursts (each burst 30 Hz, more 30 Hz, more 30 Hz, more 30 Hz, more contains one or preferably 5 to preferably 5 to preferably 5 to preferably 5 to more pulses) 15 Hz) 15 Hz) 15 Hz) 15 Hz) Number of pulses 1 to 20 1 to 20 1 to 20 1 to 20 in each burst Ramping No ramping (all No ramping (all No ramping (all No ramping (all pulses are equal pulses are equal pulses are equal pulses are equal in amplitude), in amplitude), in amplitude), in amplitude), ramping up (first ramping up (first ramping up (first ramping up (first pulse is less than pulse is less than pulse is less than pulse is less than the last pulse in the last pulse in the last pulse in the last pulse in the burst), the burst), the burst), the burst), ramping down ramping down ramping down ramping down (first pulse is (first pulse is (first pulse is (first pulse is more than the last more than the last more than the last more than the last pulse in the burst) pulse in the burst) pulse in the burst) pulse in the burst) Shape of each Square, Square, Square, Square, pulse in the pulse Trapezoidal, Trapezoidal, Trapezoidal, Trapezoidal, burst Sinusoidal Sinusoidal Sinusoidal Sinusoidal Generated EMF 1 microTesla to 1 microTesla to 1 microTesla to 1 microTesla to field over the 10 milliTesla 10 milliTesla 10 milliTesla 10 milliTesla surface area of the coil and extending outward from the surface of the coil in a range of 0 mm to 20 mm
Controller Software
(85) In one embodiment, the treatment systems disclosed herein, including the coils, coil arrays, and controller circuit configured to generate and deliver electrical current to the coils and coil arrays, are controlled by a software application configured to be installed and execute on a separate computing device, such as a mobile phone, laptop, or external controller, that is in wired or wireless communication with the controller circuit.
(86) In one embodiment, the software application, or controller application, is configured to identify a type of coil system being used by a patient. Operationally, the controller application may be installed on a mobile phone and be configured to use a camera functionality of the mobile phone to capture a bar code, QR code, or other identification or be configured to generate a graphical user interface to receive an alphanumeric identifier of the coil system. Based on the data provided, the controller application may 1) validate the coil system as being a legitimate, authorized, or otherwise acceptable coil system, 2) determine what type of coil system is being used and whether that coil system is specific to a particular anatomical region, e.g. a coil system specific to a neck region, torso region, back region, leg region, foot region, arm region, head region, or other anatomical region, and 3) based upon that determination, generate graphical user interfaces that display anatomical regions specific to the coil system being used, e.g. if the coil system is specific to a neck region the generated graphical user interfaces visually display a neck, if the coil system is specific to a torso region the generated graphical user interfaces visually display a torso, if the coil system is specific to a back region the generated graphical user interfaces visually display a back region, if the coil system is specific to a leg region the generated graphical user interfaces visually display a leg region, if the coil system is specific to a foot region the generated graphical user interfaces visually display one or more feet, if the coil system is specific to an arm region the generated graphical user interfaces visually display one or more arms, and if the coil system is specific to a head region the generated graphical user interfaces (GUIs) visually display a head region.
(87) In one embodiment, the generated GUIs are configured to receive an input from a patient as to a locus or loci of pain relative to the displayed anatomical region. For example, upon displaying the anatomical region in a GUI, a patient may paint, using a stylet or finger pressed upon a display, an area of the anatomical region that may be in pain. One or more GUIs may then be presented to prompt from a patient, and receive from the patient, an indication of the level of the pain via, for example, a visual analog scale where a user may indicate using numbers or icons a degree of the pain.
(88) Based upon the highlighted anatomical region and the level of pain, the controller software determines 1) a desired level of magnetic flux to be delivered, 2) a corresponding set of coils to be energized in what order and at what frequency, and 3) a level of current to be delivered to each coil or coil array to generate the desired level of magnetic flux in the right location and at the right frequency. In particular, different locus or loci of pain may require an increased or decreased intensity or frequency of magnetic flux to be delivered at nerves located upstream or downstream from the locus or loci of pain. The controller software therefore comprises programmatic instructions, and supporting data, that correlates anatomical locations of pain with nerve areas that are co-located with the locus or loci of pain, upstream from the locus or loci of pain and/or downstream from the locus or loci of pain. In one embodiment, the controller software becomes aware of the location of specific coils or coil arrays based on at least one of 1) a preset relationship of the coils/coil arrays that is stored and known to the controller software based on identifying the type of coil system or 2) input by a user that indicates to the controller software where each of the coils are being positioned on a patient—such an indication being provided through a GUI that presents possible anatomical locations either through text or graphically.
(89) In one embodiment, the software application, or controller application, is configured to generate instructions that, when communicated to and executed by the controller circuit, causes the controller circuit to generate electrical current and deliver that electrical current to different coils and/or coil arrays based on the desired frequency, intensity level, order, and location, as described above. For example, if a patient is suffering from acute pain on top of his or her right foot, the controller software may determine that coil arrays positioned on top of his or her right foot need to generate a magnetic flux in a range of 100 microTesla at a frequency of 10 Hz while coils positioned in the sole of the footwear, proximate the bottom of the patient's foot, need only be activated to generate a magnetic flux in a range of 20 microTesla at a frequency of 30 Hz.
(90) In another embodiment, the controller circuit may be configured to electrically connect with a coil array or coils and upon making such a connection, to detect and store an identifier of the coil array or coil. The controller circuit preferably stores each of the identifiers and communicates it to the controller software upon connecting. These identifiers may be further used to identify the validity and/or type of coils or coil arrays being used.
(91) To determine desired dosing levels, in another embodiment, the controller software may include a set of programmatic instructions for dose training. In one embodiment, the controller software operates in a training mode in which 1) a user is prompted to provide real-time feedback on pain levels using a visual analog scale, 2) the controller software modulates, over predefined periods of time, the frequency of pulse signals, the amount of current (and therefore magnetic flux intensity level) and/or the shape of the pulse signals in various combinations over the predefined period of time, and 3) as the parameters change, the user is prompted to input feedback on pain levels through the visual analog scale. For example, once a user identifies a locus of loci of pain, it initiates a cycling process starting with a set of frequency and modulating the current level and therefore the magnetic flux level up and down, prompting the user for feedback on pain levels during the cycling process. The controller software may then change frequency settings and repeat the up and down modulation of current level and magnetic flux level, again concurrently prompting the user for feedback on pain levels during the cycling process. Once the cycling processes are completed, the controller software analyzes the user's feedback to determine an optimal combination of frequency and current level for a given locus or loci of pain.
(92) Integration of Planar Microcoils with Clothing
(93) To improve patient compliance and provide for ease of use, the patches comprising planar microcoil arrays are integrated into clothing. Referring to
(94) It should be appreciated that the array sizes may be variable. For example, as shown in each of the
(95) It should further be appreciated that the planar microcoil arrays are preferably integrated into a layer of the clothing and are not directly exposed to the user's skin or to the outside environment. Referring to the shirt, head covering, foot covering, and hand coverings shown in
(96) Footwear
(97) In one embodiment, the present invention is directed toward the integration of coils and/or coil arrays into footwear, such as a shoe, boot, sock, or other foot covering. The sole or base of the footwear 1401 comprises a plurality of individual coils, such as Coil S.sub.1, Coil S.sub.2, and Coil S.sub.3, and/or coil arrays, such as Array S.sub.1 that are distributed on a surface of the sole or base. The individual coils, such as Coil S.sub.1, Coil S.sub.2, and Coil S.sub.3, and/or coil arrays, such as Array S.sub.1 may be of the type described herein or 1. Coil S.sub.1: 6 by 5 cm, inner air core: 0.2 by 1.2 cm, 800 to 1,500 turns (preferably 1200-1300 turns), 0.04 mm wire thickness or larger. 2. Coil S.sub.2: 7 by 5.1 cm, inner air core: 0.2 by 2.3 cm, 800 to 1500 turns (preferably 1200-1300 turns), 0.04 mm wire thickness or larger. 3. Coil S.sub.3: 3 by 4.5 cm, inner air core: 0.2 by 1.7 cm, 700 turns, 0.04 mm wire thickness
(98) Preferably, the individual coils, such as Coil S.sub.1, Coil S.sub.2, and Coil S.sub.3, and/or coil arrays, such as Array S.sub.1 are configured to be of different sizes with Coil S.sub.1 being larger or having more windings than Coil S.sub.2 or Coil S.sub.3 and where a distance between the Coil S.sub.1, Coil S.sub.2, and Coil S.sub.3 is between 1 cm and 3 cm, preferably around 2 cm. Each of the Coil S.sub.1, Coil S.sub.2, and Coil S.sub.3 are in electrical communication with the controller 1403. The controller 1403 is also in electrical communication with a plurality of coil arrays U.sub.1, U.sub.2, U.sub.3, U.sub.4, U.sub.5, and/or U.sub.6 1402 that are integrated into the upper of the footwear and configured to cover the entirety of the user's foot. As discussed above, each of the coil arrays may be energized and/or controller as described above to address a user's foot pain.
(99) Optionally, the ankle region of the footwear device may comprise two large coils which are positioned on opposing sides of the ankle region and are spaced and sized to function as Helmholtz coils.
(100) Referring to
(101) Referring to
(102) It should be appreciated that, upon activation, magnetic fields are generated in accordance with the stimulation protocols described above. Conventionally, it is believed that very large magnetic fields have to be directed into the brain to have any tangible therapeutic effects on certain conditions, such as depression. However, it is believed that, by modulating a position, configuration, orientation, or movement, of magnetite chains in one or more brain cells or neurons, which may be effectuated by magnetic fields less than 100 microTesla or by applying a sufficient magnetic field gradient, which is determined by the frequency and shape of pulse, one can cause a normalization of magnetite functionality, at least during the application of the magnetic fields. Normalization of magnetite functionality may thereby enable at least a partial alleviation of symptoms associated with anxiety disorders, obsessive compulsive disorder, post-traumatic stress disorder, memory degeneration, schizophrenia, Parkinson's disease, stroke rehabilitation, drug addiction, including addiction to, or cravings for, nicotine, cocaine, alcohol, heroine, methamphetamines, stimulants, and/or sedatives, depression and depression-related conditions, such as post-partum depression or bipolar depression, auditory hallucinations, multiple sclerosis, fibromyalgia, Alzheimer's disease, spinocerebellar degeneration, epilepsy, urinary incontinence, movement disorders, chronic tinnitus, or sleep apnea while the magnetic fields are being applied to the brain. Accordingly, it is within the scope of this invention to treat symptoms related to disorders having a loci of dysfunction in the brain by normalizing at least one of a position, configuration, orientation, or movement of magnetite chains in one or more brain cells or neurons by applying magnetic fields less than 100 microTesla or by applying a sufficient magnetic field gradient.
(103) It should further be appreciated that other embodiments may be specifically designed to be directed toward 1) treating osteoporosis by, for example, positioning a plurality of arrays along a length of substrate configured to extend over an entire length of a user's spine, each of said arrays being in electrical communication with a controller, 2) effectuating an activation of acupoints that may be distributed over various areas of the user's body, where at each acupoint an array is positioned and where all of the arrays are in electrical communication with a controller; optionally, a coil that aligns with an acupoint may be configured to receive a higher level of current and generate a higher magnetic flux than the rest of the coils which are not aligned with an acupoint, 3) treating a neck region to reduce increase and increase a collagen framework, where a plurality of arrays are configured to extend around a neck region of the user, each of the arrays being in electrical communication with a controller, and 4) treating one or more broken bones by providing a plurality of arrays configured to be positioned on a user's skin and between a cast and the user's skin, each of the arrays being electrical communication with a controller.
(104) Referring to
(105) The condition is at least one of an anxiety disorder, an obsessive compulsive disorder, a post-traumatic stress disorder, memory degeneration, schizophrenia, Parkinson's disease, stroke rehabilitation, drug addiction, drug cravings, depression, depression-related conditions, post-partum depression, bipolar depression, auditory hallucinations, multiple sclerosis, fibromyalgia, Alzheimer's disease, spinocerebellar degeneration, epilepsy, urinary incontinence, movement disorders, chronic tinnitus, or sleep apnea.
(106) The article of clothing may be attached such that at least one of the two or more planar microcoils in at least one of the plurality of planar microcoil arrays is positioned over an acupoint of the patient's body. Additionally, prior to attaching the article of clothing, a skin impedance measurement may be made and, based on the level of impedance, the article of clothing may be attached such that at least one of the two or more planar microcoils in at least one of the plurality of planar microcoil arrays is positioned over an area of impedance that exceeds a predefined threshold value. Accordingly, an impedance measurement sensor and circuit may also be integrated into the article of clothing.
(107) While the exemplary embodiments of the present invention are described and illustrated herein, it will be appreciated that they are merely illustrative. It will be understood by those skilled in the art that various changes in form and detail may be made therein without departing from or offending the spirit and scope of the invention.