SUPPORTING DEVICE FOR SUPPORTING A BODY PART OF A USER
20210330265 · 2021-10-28
Inventors
Cpc classification
A61B5/6887
HUMAN NECESSITIES
A61F2/76
HUMAN NECESSITIES
A61F7/03
HUMAN NECESSITIES
A61B5/7455
HUMAN NECESSITIES
A61H2201/10
HUMAN NECESSITIES
A61H2201/169
HUMAN NECESSITIES
A61F5/00
HUMAN NECESSITIES
A61B5/0205
HUMAN NECESSITIES
A61B5/0022
HUMAN NECESSITIES
A61H1/00
HUMAN NECESSITIES
A61B5/0004
HUMAN NECESSITIES
A61F7/02
HUMAN NECESSITIES
A61H2201/1654
HUMAN NECESSITIES
G06F3/016
PHYSICS
A61F2007/0071
HUMAN NECESSITIES
A61H2201/501
HUMAN NECESSITIES
International classification
A61B5/00
HUMAN NECESSITIES
A61B5/0205
HUMAN NECESSITIES
A61F7/00
HUMAN NECESSITIES
Abstract
Support device (1) for supporting at least one body part of a user at least in portions, optionally completely, comprising a support body (2), which comprises at least one support region (3) for supporting at least one body part of a user at least in portions, optionally completely, wherein at least the support region (3) has, at least in portions, optionally completely, a geometric-structural design that is individually configured on the basis of the data describing at least one body part of a user that is to be supported on the support region (3) at least in portions, optionally completely.
Claims
1. A support device (1) for supporting at least one body part of a user at least in portions comprising: a support body (2), which comprises at least one support region (3) for supporting at least one body part of a user at least in portions, wherein at least the support region (3) has, at least in portions, geometric-structural design that is individually configured on the basis of the data describing at least one body part of a user that is to be supported on the support region (3) at least in portions.
2. The support device according to claim 1, wherein the support region (3) comprises one or more individually configured support-region portions (5), which are designed as receiving portions (4) and are configured to receive a particular body part of a body part that is supported or is to be supported on the support region (3).
3. The support device according to claim 1, comprising a detection device (7), integrated in the support region (3) and/or the support body (2), configured to detect at least one one of a chemical and physical variable of at least one of the support region (3), the support body (2), and a body part supported on the support region (3).
4. The support device according to claim 3, comprising a transmission device (8), which is or can be assigned to the detection device (7), integrated in at least one of the support region (3) and the support body (2), and configured to transmit a piece of detection information describing the at least one of the chemical and physical variable detected by means of the detection device (7) to at least one communication partner (19).
5. The support device according to claim 1, comprising a detection device (9), integrated in at least one of the support region (3) and the support body (2), configured to detect a body part supported on the support region (3).
6. The support device according to claim 5, comprising a transmission device (8), which is or can be assigned to the detection device (9), integrated in the at least one of the support region (3) and the support body (2), and configured to transmit a piece of detection information describing a body part supported on the support region (3) detected by means of the detection device (9) to at least one communication partner (19).
7. The support device according to claim 1, comprising a detection device (10), integrated in the at least one of the support region (3) and the support body (2), configured to detect at least one of a blood pressure, an oxygen saturation, and a pulse, of a user supporting a body part on the support region (3).
8. The support device according to claim 7, comprising a transmission device (8), which is or can be assigned to the detection device (10), integrated in the at least one of the support region (3) and the support body (2), and configured to transmit a piece of detection information describing the at least one of the blood pressure, the oxygen saturation, and the pulse detected by means of the detection device (10) to at least one communication partner (19).
9. The support device according to claim 1, comprising a detection device (11), integrated in the at least one of the support region (3) and the support body (2), configured to detect at least one of a movement of the support body (2) in at least one degree of freedom, relative to a surface and a movement of a body part supported on the support region (3) in at least one degree of freedom, relative to the support body (2).
10. The support device according to claim 9, comprising a transmission device (8), which is or can be assigned to the detection device (11), is integrated in the at least one of the support region (3) and the support body (2), configured to transmit at least one of the movement, detected by means of the detection apparatus (11), of the support body (2) in at least one degree of freedom, relative to a surface and the movement, detected by means of the detection apparatus (11), of a body part supported on the support region (3) in at least one degree of freedom, relative to the support body (2), to at least one communication partner (19).
11. The support device according to claim 3, comprising a storage device (12), integrated in the at least one of the support region (3) and the support body (2), is configured to store at least one piece of detection information detected by means of the detection device (7, 9, 10, 11).
12. The support device according to claim 1, comprising a signal-output device (13), integrated in the at least one of the support region (3) and the support body (2), configured to generate at least one of an acoustic, an optical, and a haptic output signal, on the basis of at least one piece of detection information generated by the or a detection device (7, 9, 10, 11).
13. The support device according to claim 12, wherein the at least one of the acoustic, the optical, and the haptic output signal contains at least one piece of information relating to at least one of a user-side action and an evaluation of a user-side action, on a user, of the support device (1).
14. The support device according to claim 1, wherein the support body (2) is integrated at least in portions in an input apparatus (15) of a device that can be controlled by the input apparatus (15).
15. The support device according to claim 1, comprising a temperature-control device (16), integrated in the at least one of the support region (3) and the support body (2), for controlling at least one of the temperature of the support region (3) and the support body (2) at least in portions.
16. The support device according to claim 15, wherein the temperature-control device (16) comprises a temperature-control duct structure comprising a temperature-control duct through which a temperature-control medium can flow.
17. The support device according to claim 16, wherein the temperature-control device (16) comprises at least one electrically operated temperature-control element.
18. The support device according to claim 14, wherein the temperature-control device (16) comprises at least one temperature-control element, which performs an exothermic chemical reaction after activation.
19. The support device according to claim 1, comprising a fixing device, which is or can be assigned to at least one of the support body (2) and the support region (3), for temporarily fixing a body part supported on the support region (3) in an intended support position of the body part on the support region (3).
20. The support device according to claim 1, wherein the support body (3) comprises a mounting portion (17) for mounting the support body (2) on a surface.
21. The support device according to claim 20, wherein the mounting portion (17) comprises at least one mounting-portion element (18) which lies in a non-planar manner on a planar surface and makes it possible to mount the support body (2) that is mounted on the surface relative to the surface so as to be pivotally movable, in at least one degree of freedom.
22. The support device according to claim 1, wherein the support region (3) is a component that is separate from the support body (2) and can be connected to the support body (2) so as to form the support device (1).
23. The support device according to claim 1, comprising at least one support element (21), which is detachabley supported on the support region (3) so as to cover said support region at least in portions.
24. The support device according to claim 1, wherein the at least one of the support region (3) and the support body (2) comprises at least one magnetisable or magnetic material.
25. The support device according to claim 1, wherein the at least one of the support region (3) and the support body (2) comprises at least one antibacterial material.
26. The support device according to claim 1, wherein the at least one of the support region (3) and the support body (2) is additively manufactured at least in portions.
27. A communication system (20) comprising: at least one support device (1) according to claim 1, which comprises a transmission device (8), configured to transmit a piece of information to at least one communication partner (19) and/or to receive a piece of information transmitted by at least one communication partner (19), and at least one communication partner (19), which is configured to receive a piece of information transmitted by the at least one support device (1) and/or to transmit a piece of information to the at least one support device (1).
28. A method for producing a support device (1) according to claim 1, comprising the steps of: providing data describing at least one body part of a user that is to be supported on the support region (3) of the support device (1) to be produced at least in portions, and producing at least the support region (3) on the basis of the data such that the support region (3) has, at least in portions, a geometric-structural design that is individually configured on the basis of the data.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0069] The support devices described herein are explained in greater detail on the basis of embodiments in the drawings, in which:
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DETAILED DESCRIPTION
[0083]
[0084] The support device 1 comprises a support body 2. The support body 2, which can also be referred to as or considered to be a mounting body, also comprises a support region 3, which can also be referred to as or considered to be a mounting region, for supporting a body part of a user. The support region 3 is therefore understood to be the region of the support device 1 on which a user (directly) supports a body part when the support device 1 is used as intended. The support region 3 therefore constitutes the actual region of the support device 1 on which a user supports or mounts a body part when the support device 1 is used as intended. As shown in
[0085] As shown in
[0086] The dimensions of the support device 1, the support body 2 and the support region 3 are typically adapted to the dimensions of the body part to be supported in each case. When the support device 1 is used as intended, the support region 3 can be completely covered by the body part being supported in each case.
[0087] The support device 1 is characterised in that the support region 3 has a geometric-structural design that is individually configured on the basis of the data describing the body part of a user that is to be supported on the support region 3. The support region 3 therefore has an individually configured geometric-structural design and thus has a high degree of customisation. The support region 3, and optionally also the support body 2 and thus also the support device 1, may therefore be a component that is individually configured or individually configurable for a particular body part of a particular user.
[0088] The individually configured geometric-structural design of the support region 3, with this in particular being understood to be particular contours or structures of the surface of the support region 3, has been produced on the basis of the data describing at least one body part of a particular user that is to be supported on the support region 3 when used as intended. The support region 3 therefore typically constitutes a (negative) reproduction, individually configured in a user-specific manner, of a body part of a particular user that is to be supported on the support region 3. This allows for a fit of the support region 3 that is individually configured in a user-specific manner or a manner specific to a body part of the user and is thus highly precise, this fit allowing the relevant body part to be supported on the support region 3 in a relaxing or relaxed position specific to this body part.
[0089] Supporting a body part in a relaxing or relaxed position specific to this body part can both have a relaxing effect on the relevant body part as well as on other body parts adjacent to this body part, such that the user's whole body can be brought into a relaxing or relaxed state when using the support device 1. In addition to the mere relaxing effect or as a consequence thereof, where necessary, therapeutic effects can also be brought about, since supporting the body part in a relaxing or relaxed position specific to this body part can e.g. have a therapeutic effect on the blood flow and/or oxygen supply to the relevant body part. Likewise, the effect of reducing swelling could also be demonstrated. Positive effects could be identified in particular in rheumatic body parts or limbs and/or in e.g. spastic body parts or limbs due to a stroke. The increase in the internal tension (tone) of the muscles of the relevant body part, associated with spasticity, could be reduced (significantly in some cases) by (regular) use of the support device 1.
[0090] The user can use the support device 1 in particular without any help from a third party; therefore, the user can independently carry out therapeutic measures, i.e. for regulating tone, pain therapy, etc., and prepare themselves for corresponding therapeutic measures in the sense of self-help by using the support device 1 as intended.
[0091] Using the example of a spastic hand, the support device 1, which, in this respect, can be referred to as or considered to be a customised support for the heel of the hand for providing therapy to persons with a spastic or cramped hand, makes it possible for the hand to rest on the support or support device 1 in a loosened state. By supporting the cramped hand on the customised support surface, a state of relaxation is achieved. The hand is reproduced and positioned by the shape of the customised support for the heel of the hand with a precise fit.
[0092] With reference to
[0093] On the basis of
[0094] In this last-mentioned variant, the support body 2 and/or the support region 3 may comprise suitable, optionally corresponding, connection elements (not shown), which allow for a stable, but nevertheless typically detachable (without being damaged or destroyed) connection of the support body 2 to the support region 3, and vice versa. The support body 2 may e.g. comprise at least one first connection element and the support region 3 may comprise at least one second connection element, the at least one first and the at least one second connection element being configured to interact with one another so as to form the support device 1. The at least one first connection element and the at least one second connection element may e.g. be configured to interact with one another in a form-fitting and/or force-locked manner so as to form the support device 1. It is also conceivable for the at least one first connection element and the at least one second connection element to be configured to interact with one another magnetically so as to form the support device 1.
[0095] With reference to
[0096] In the embodiment, shown in
[0097] Specifically, the embodiment according to
[0098] The individually configured geometric-structural design, i.e. in particular geometric-structural parameters such as length, height, width, etc., of relevant receiving portions 4 is therefore adapted to or modelled on the anatomical form or morphology of the relevant body part to be received in the relevant receiving portion 4; the individually configured geometric-structural design of the relevant receiving portion 4 is therefore produced in respect of the morphology of a body part to be received therein. With reference to
[0099] In the embodiment, shown in
[0100]
[0101] With reference to the embodiment shown in
[0102] With reference to
[0103] With reference to
[0104] With reference to
[0105] As shown by the box formed by dashed lines, the detection devices 7, 9, 10, 11 may also be combined in a common detection device in terms of hardware and/or software.
[0106] With reference to
[0107] With reference to
[0108] With reference to
[0109] An output signal which can be output by means of a signal-output device 13, by way of example, may contain at least one piece of information relating to a user-side action and/or an evaluation of a user-side action, in particular on a user, of the support device 1. In this way, it is possible to assist a user in properly using the support device 1 by means of corresponding output signals containing corresponding information. For example, it can be output to a user by corresponding output signals that the support device 1 is ready to support a body part, and optionally also which body part, that a body part is properly supported or is not (yet) properly supported, or when/that a particular support duration, e.g. expedient for a therapeutic effect, has been reached or has not (yet) been reached, etc. Equally, output signals that encourage or motivate a user are conceivable, i.e. output signals that encourage or motivate a user, e.g. acoustically, optically or haptically, to use the support device 1, to assume and/or maintain a particular support position, etc. Similarly, output signals that assess, i.e. in particular praise or criticise, a user are conceivable, which signals assess a user or a particular user action, e.g. acoustically, optically or haptically, before and/or during and/or after use of the support device 1.
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[0111] With reference to
[0112]
[0113] With reference to
[0114] A corresponding temperature-control device 16 may comprise a temperature-control duct structure comprising a temperature-control duct through which a temperature-control medium, i.e. a gas or liquid, for example, can flow. A corresponding temperature-control duct structure may extend through the support body 2 or the support region 3, in particular in a planar manner, at least in portions, optionally completely. In particular, a corresponding temperature-control duct structure may extend, in particular with close contours, in the region of or below the (exposed) surface of the support body 2 or the support region 3 forming an actual support surface of the support body 2 or the support region 3.
[0115] Alternatively or additionally, a corresponding temperature-control device 16 may comprise at least one electrically operated temperature-control element (not shown). A corresponding electrically operated temperature-control element may e.g. be designed as or comprise at least one heating wire or a one-dimensional or multi-dimensional heating-wire structure. A corresponding temperature-control element may extend through the support body 2 or the support region 3, in particular in a planar manner, at least in portions, optionally completely. In particular, a corresponding temperature-control element may extend, in particular with close contours, in the region of or below the (exposed) surface of the support body 2 or the support region 3 forming an actual support surface of the support body 2 or the support region 3.
[0116] Alternatively or additionally, a corresponding temperature-control device 16 may comprise at least one temperature-control element, which performs an optionally reversible exothermic chemical reaction after activation. A corresponding temperature-control element may be arranged or formed in the region of or below the (exposed) surface of the support body 2 or the support region 3 forming an actual support surface of the support body 2 or the support region 3. A corresponding temperature-control element may comprise an activation element (not shown), i.e. a tab, a button, etc., by means of which it is possible to activate the temperature-control element, i.e. to initiate the exothermic reaction.
[0117]
[0118] With reference to
[0119] A corresponding mounting portion 17 may be provided with or comprise at least one material or corresponding material structure that provides non-slip support of the support body 2 on a surface or a base. For example, a corresponding material or a corresponding material structure may therefore be expedient for allowing the support body 2 to be supported in a stable manner on a surface or a base. A corresponding material or a corresponding material structure may e.g. be made of an elastomer material or an elastomer material structure or may comprise at least one elastomer material. In principle, both natural and synthetic elastomer materials or material structures are possible. In terms of manufacturing, thermoplastic elastomers may advantageously be used, for example.
[0120] A corresponding mounting portion 17 may be provided with or comprise at least one reversibly deformable material, in particular a reversibly deformable, flexible material, or a reversibly deformable material structure, in particular a reversibly deformable, flexible material structure. For example, a corresponding material or a corresponding material structure may therefore be expedient to allow any required modifications to the orientation of the support body 2 on a surface or a base, in particular relative to a neutral or reference orientation, which, for example, can make it easier or make it possible for users with spastic body parts or limbs to use the support device 1; this is particularly applicable if the spasticity in question or another anatomical malalignment requires a particular orientation of the support body 2, in particular relative to a neutral or reference orientation, in order to support the body part on the support region 3, in particular without causing any pain. A corresponding material or a corresponding material structure may e.g. be made of an elastomer or cellular material or an elastomer or cellular material structure or may comprise at least one elastomer material. In principle, both natural and synthetic elastomer or cellular materials or material structures are possible. In terms of manufacturing, optionally foamed, thermoplastic elastomers may advantageously be used, for example.
[0121] A corresponding mounting portion 17 may, as shown in
[0122] A corresponding mounting-portion element 18 may also be designed as a separate component and, when required, is or can be connected, optionally in a detachable manner (without being damaged or destroyed), to the support body 2 so as to form the support device 1. A corresponding, e.g. spherical, hemispherical, cylindrical or semi-cylindrical or pyramidal mounting-portion element 18 may e.g. be connected to the support body 2 by a hook-and-loop fastener system or an interchangeable fastener system.
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[0124] With reference to
[0125] Although not shown in the drawings, the support device 1 may comprise a fixing device, which is or can be assigned to the support body 2 and/or the support region 3, for temporarily fixing a body part supported on the support region 3, in particular in an intended support position of the body part on the support region 3. Corresponding fixing may facilitate and maintain a desired orientation of a body part supported on the support region 3. In this way, a relaxation effect or therapeutic effect that can be produced by the support device 1 can be assisted. A corresponding fixing device can make it possible to fix a relevant body part directly to the support body 2 or the support region 3; this may e.g. be implemented by a fixing element that is or can be attached to the support body 2 or the support region 3, such as a strap, a loop, etc., which surrounds the relevant body part at least in portions, optionally completely, after being put on, such that the body part is fixed to the support body 2 or the support region 3. A tube-like or tubular fixing device is also conceivable, i.e. a fixing tube made of a fabric, for example, which can be pulled over the support device and the body part that is supported or is to be supported thereon and, in this way, a desired orientation of a body part supported on the support region is facilitated and maintained. A fixing device is also conceivable which makes it possible to fix a superordinate body part, i.e. an arm, for example, in a particular orientation when the body part to be fixed is a hand.
[0126] It is applicable to all the embodiments that the support region 3 and/or the support body 2 is made of or comprises at least one magnetisable or magnetic material. Magnetisable or magnetic materials, such as corresponding ferromagnetic metals, may have a positive effect on the blood flow through the corresponding body part, and this can promote therapeutic effects. Magnetisable or magnetic materials may be provided as a solid material or in the form of particles.
[0127] It is also applicable to all the embodiments that the support region 3 and/or the support body 2 is, alternatively or additionally, made of or comprises at least one antibacterial material. Antibacterial materials, such as antibacterial metals, may have a positive effect on the hygienic properties of the support region 3 and/or the support body 2. Antibacterial materials may be provided as a solid material or in the form of particles.
[0128] With regard to the production of the support device 1, i.e. the support body 2 and/or the support region 3, in principle any manufacturing methods, in particular moulding and/or shaping manufacturing methods, are taken into consideration.
[0129] In particular, both additive (build-up) manufacturing methods and subtractive (material-removing) manufacturing methods, i.e. in particular machining manufacturing methods, are taken into consideration.
[0130] Additive manufacturing methods may be particularly expedient, since these are particularly suitable for producing corresponding, individually configured geometric-structural designs. Therefore, additive manufacturing methods can be taken into consideration which allow for the additive build-up of three-dimensional objects by selectively hardening, in layers, an optionally powdered construction material that can be selectively hardened in layers (this may e.g. be a metal or a plastics material) by means of radiation energy, i.e. in particular by means of at least one energy beam. Merely by way of example, in this connection reference is made to binder-jetting methods, selective laser-melting methods, selective laser-sintering methods or sterolithography methods.
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[0132] The communication partner 19 may e.g. be a mobile terminal, such as a portable computer (laptop), a smartphone, a tablet, or smart glasses, may be a stationary terminal, such as a stationary computer (desktop, server), may be a network application, or may be network storage (cloud), etc.
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[0134] The method serves to produce a support device 1 for supporting at least one body part of a user at least in portions, optionally completely, comprising a support body 2, which comprises at least one support region 3 for supporting at least one body part of a user at least in portions, optionally completely.
[0135] The method comprises the step S1, i.e. providing data describing at least one body part of a user that is to be supported on the support region 3 of the support device 1 to be produced at least in portions, optionally completely, and the step S2, i.e. producing at least the support region 3 on the basis of the data such that the support region 3 has, at least in portions, optionally completely, a geometric-structural design that is individually configured on the basis of the data.
[0136] The method may further comprise a step S1′, i.e. recording data describing at least one body part of a user that is to be supported on the support region 3 at least in portions, optionally completely. Recording corresponding data that corresponds to the subsequent provision may therefore be part of the method.
[0137] The support region 3 and/or the support body 2 may in particular be produced by means of an additive manufacturing method.
[0138] Individual features, multiple features or all the features disclosed in connection with a particular embodiment may be combined with individual features, multiple features or all the features disclosed in connection with at least one other embodiment.