The present invention relates to posture support devices and more particularly to posture support devices that are wearable.
It is generally recognized that poor posture can lead to several painful conditions over time. To assist in preventing poor posture several manufacturers have developed posture support devices for wear by people, and which are intended to improve the posture of the wearers. All of these devices, however, can create other problems for the wearer, such as reduced blood flow and such as painful compression of certain regions of the body of the wearer.
There is therefore a need for an improved posture support device.
In a first aspect, the invention is directed to a posture support device for a wearer, including an anchor member, a first strap and a second strap. The anchor member is fittable around the torso of the wearer. Each strap has a first end and a second end and connects to the anchor member at the first and second ends. Each strap has a shoulder-engaging portion that is shaped to engage a shoulder joint of the wearer. The straps are each adapted to carry a tensile force and thereby exert a rearward force on the shoulder joint through the shoulder-engaging portion. The straps are configured to engage the shoulders of the wearer no further medially than the acromioclavicular joints. Each strap extends along a path that, in use, does not cross over the anterior axillary folds of the wearer.
In a second aspect, the invention is directed to a posture support device for a wearer, wherein the posture support device is configured to urge the shoulders of the wearer rearward while avoiding exerting a downward force on the clavicles of the wearer, and while avoiding crossing over the anterior axillary folds of the wearer.
In a third aspect, a posture support device for a wearer, including an anchor member, a first strap and a second strap. The anchor member is fittable around the torso of a wearer. Each strap has a first end and a second end and connects to the anchor member at the first and second ends. Each strap has a shoulder-engaging portion that is shaped to engage a shoulder joint of the wearer. The straps are each adapted to carry a tensile force and thereby exert a rearward force on the shoulder joint through the shoulder-engaging portion. The straps are configured to engage the shoulders of the wearer no further medially than the acromioclavicular joints. The posture support device is free of any tension bearing members that encircle the thorax of the wearer either alone or in combination, thereby facilitating expansion of the rib cage during breathing.
In one embodiment of the third aspect, the anchor member has an upper edge which extends across the front of the torso of the wearer below the xiphoid process and no lower than the bottom rib and wherein the anchor member is adapted to carry a tensile force and thereby urge the ribs upwards in use to increase the volume of the thoracic cage.
In a fourth aspect, the invention is directed to a posture support device for a wearer, including an anchor member, a first strap and a second strap. The anchor member is fittable around the torso of the wearer. Each strap has a first end and a second end and connects to the anchor member at the first and second ends. Each strap has a shoulder-engaging portion that is shaped to engage a shoulder joint of the wearer. The straps are each adapted to carry a tensile force and thereby exert a rearward force on the shoulder joint through the shoulder-engaging portion. The straps are configured to engage the shoulders of the wearer no further medially than the acromioclavicular joints. The posture support device further comprises at least one covering panel. The at least one covering panel is connected to at least one of the anchor member, the first strap and the second strap while transferring substantially no force between the wearer and any of the anchor member, the first strap or the second strap. The at least one covering panel is configured to cover portions of the body of the wearer which the anchor member and the first and second straps are not configured to cover.
The present invention will now be described by way of example only with reference to the attached drawings, in which:
a is a perspective view of a person exhibiting good posture, in accordance with the prior art;
b is a rear elevation view of the person shown in
c is a magnified rear elevation view of a scapula, a clavicle, a humerus and a sternum from the person shown in
d is a magnified rear elevation view of some of the muscles, neurovascular structures and skeletal structure of the person shown in
e is a front elevation view of some of the internal musculature on the person shown in
f is a front elevation view of some of the skeletal structure of the person shown in
a is a rear elevation view of person shown in
b is a front elevation view of the skeletal structure shown in
a is a front elevation view of a support device in accordance with an embodiment of the present invention;
b is a front elevation view of the support device shown in
c is a rear elevation view of the support device shown in
d is a magnified front elevation view of a portion of the support device shown in
e is a front elevation view of the support device shown in
f is a rear elevation view of the support device shown in
g is a front elevation view of a the support device shown in
a is a front elevation view of a support device in accordance with another embodiment of the present invention, being worn by a wearer;
b is a rear elevation view of the support device shown in
a is a front elevation view of a support device in accordance with another embodiment of the present invention, being worn by a wearer;
b is a rear perspective view of the support device shown in
c is a rear perspective view of the support device shown in
For purposes of clarity the terms ‘circumference’ and ‘effective circumference’ are used herein to refer to the distance around the perimeter of an object or a portion of the human body, even though the object or the body portion may not be perfectly circular.
Reference is made to
Referring to
The first rib is shown at 26a in
Referring to
Referring to
Referring to
Several neurovascular structures pass underneath the pectoralis minor tendon 47, including the brachial plexus and the axillo-subclavian artery and vein. These neurovascular structures are identified at 27.
Referring to
Referring to
Additionally, referring to
Referring to
In a slouched, or round-shouldered, position, the body, and in particular, the spine 24 no longer has an S-shaped configuration. As a result, pressure is distributed between the vertebrae and the discs of the spine 24 in such a way as to urge the discs to bulge, which can, over time, lead to several problems, which are known to persons skilled in the art.
A round-shouldered posture may be acquired as a result of lifestyle and/or occupation. For example, in some types of employment, a person 10 uses their pectoral muscles 45 and 74 predominantly and the periscapular muscles and lumbar extensors are typically neglected, resulting in what is called deconditioning. In a deconditioned state the combined pull of the pectorals 45 and 74 and the failure of the periscapular muscles and lumbar extensors together create a round-shouldered posture.
As a result of the relatively poorly opposed pull of the pectorals 45 and 74, the scapula 22 becomes abducted, and thus moves outwards laterally, as shown in
It will be understood that, when compression of the neurovascular structures 44 is said to take place between the clavicle 30 and the first rib 26a, one or both of the clavicle 30 and the first rib 26a might not be in direct contact with the structures 44 that are being compressed. Other elements such as the subclavian muscle or the infraspinatus which are present in the gap may be involved in the compression.
Compression of the neurovascular structures 44 can lead to several of the ailments noted above. For example, as a result of the compression of the vascular structures that are included in the neurovascular structures 44, the resistance to fluid flow in these vascular structures increases, which results in dilation of certain veins and tributaries, and increased arterial vascular resistance due at least in part to the slowed venous flow. The consequences of venous congestion and increased arterial resistance are well known in the form of edema and ischemia first in the areas of greatest vascular impairment and later in other body regions also. Numerous ailments can result from this condition of compressed neurovascular structures 44, including, for example, migraine headaches, facial pressure, neck pain, hand and arm pain and numbness, coldness of the hands, some forms of non-radicular leg pain and intermittent numbness.
As a result of its connection with the sternum 28, the rearward movement of the first or proximal end 35 of the clavicle 30 causes the sternum 28 (and in particular, the manubrium sternum) to move rearwardly along with it, thus reducing the distance between the manubrium sternum and the anterior border of the body of T3 (the third thoracic vertebra).
In certain types of people 10 this reduction in the aforementioned diameter can lead to one or more difficulties. For example, individuals with a thin, narrow thorax tend to have a relatively straight cervical and thoracic spinal, saggital alignment. In such people, a loss of cervical lordosis and flattening of the thoracic kyphosis leads to a closer approximation of the posterior surface of the manubrium sternum to the anterior border of the body of the third thoracic vertebrae. For example, in some people this distance may be less than approximately 5 cm (2 inches). With the proximal ends 35 of the clavicles 30 urged rearwardly as described above, this distance may be reduced to approximately 2.5 cm (1 inch) to 3.8 cm (1.5 inches). This is especially true at the head of the first rib 26a which sits deeper into the thorax than the other ribs 26. This positioning of the first rib 26a permits it to compress particular veins, such as the brachiocephalic vein. Other people 10 who may be prone to incurring difficulties from the reduced ‘diameter’ include individuals who have pectus excavatum, individuals who have thoracic scoliosis, individuals who have a loss of cervical lordosis in general, and/or individuals who are obese.
In addition to causing the rotation of the clavicle 30 in the horizontal plane, the movement of the scapula 30 as a result of deconditioning can also cause a rotation of the clavicle 30 generally about its own length in a clockwise direction from a viewpoint facing the side of the left shoulder of the person 10, and in a counterclockwise direction from a viewpoint facing the side of the right shoulder of the wearer 10. Due to the configuration of the clavicle 30, this rotation further narrows the gap between the clavicle 30 and the first rib 26a, thereby adding to the compression of the neurovascular structures 44 that pass therethrough.
In addition to the above, deconditioning of the stabilizer muscles of the scapula 22 can also lead to ‘non-neurogenic winging’ of the scapula 22. Non-neurogenic winging of the scapula 22 refers to an outward movement of the medial edge of the scapula 22 away from the plane of the back 18, however, it is not caused by damage to the long thoracic nerve, which is the typical cause of neurogenic winging. Non-neurogenic winging is instead the result of the weakened state of the stabilizer muscles that hold the medial edge of the scapula 22 down in the plane of the back 18.
Non-neurogenic winging of the scapula 22 causes a rotary torque to be exerted on the acromioclavicular joint 42, which in turn causes a downward movement of the clavicle 30. This downward movement of the clavicle 30 further reduces the size of the gap, and therefore exacerbates the problem of compression of the neurovascular structures 44 that pass therethrough.
Additionally, in situations where drooping of the scapula 22 occurs as a result of deconditioning, the coracoid process 43 and, in turn, the pectoralis minor tendon 47 may be lowered relative to their normal position, whereby the pectoralis minor tendon 47 compresses the neurovascular structures 27 that pass underneath. Compression of these structures 27 results in many of the same ailments as compression of the structures 44 that pass underneath the clavicles 30.
In addition to the above, individuals 10 who have a round-shouldered posture are typically relatively sensitive along the anterior axillary fold 95, such that, any compression of the anterior axillary fold 95 results in pain.
It will be noted that movement of the scapulae 22 can impart movement to the ribs 26 by way of their connection to the ribs 26 through the scapular stabilizer muscles. Abduction of the scapulae 22, as shown in
Reference is made to
The support device 46 includes an anchor member 48, and two straps 50. Referring to
The anchor member 48 may optionally include an opening 58, which is closable by a connector 60 (
To prevent the one or more hooks 62 from disengaging from the one or more eyes 66 inadvertently, the connector 60 may be supplemented by a hook-and-loop portion 68, which is positioned proximate the hooks 62 and eyes 66. The hook-and-loop connector portion 68 includes a hook portion 68a, which may be proximate the one or more hooks 62 and a loop portion 68b, which may be positioned proximate the one or more eyes 66.
Other connectors 60 are alternatively possible. For example, the connector 60 may be made solely of a strip of hook material 68a and a strip of loop material 68b, which may form a sufficiently strong connection without the use of hooks and eyes. As yet another example of a connector 60, the connector 60 may include a zipper instead of the aforementioned hooks and eyes and instead of the aforementioned hook material and loop material.
The anchor member 48 may further include a circumference adjustment device 67, which permits the effective circumference of the anchor member 48 to be adjusted to accommodate wearers 10 of different sizes. The circumference adjustment device 67 may be made up by any suitable structure. For example, the anchor member 48 may include a plurality of sets 65 of one or more eyes 66, wherein each set 65 is positioned at a different distance from the second edge 59b. For example, a first set 65 may be positioned approximately 1 cm from the second edge 59b, a second set 65 may be positioned approximately 3 cm from the second edge 59b. The set 61 of one or more hooks 62 could be insertable into any set 65 of one or more eyes 66, thereby adjusting the effective circumference of the anchor member 48.
It is alternatively possible to provide the one or more hooks 62 proximate the second edge 59b and to provide the one or more eyes 66 proximate the first edge 59a.
It is alternatively possible for the circumference adjustment device 67 to include a plurality of sets 61 of hooks 62, wherein the sets 61 are positioned at different distances from their respective end 59a or 59b of the anchor member 48, and to include a single set 65 of eyes 66 proximate the other end 59a or 59b of the anchor member 48. It is further alternatively possible for the circumference adjustment device 67 to include a plurality of sets 61 of hooks 62 and a plurality of sets 65 of eyes 66.
If strips of hook material 68a and loop material 68b are included in the connector 60, these strips 68a and 68b can be made to engage each other no matter which set 61 of hooks 62 and which set 65 of eyes 66 are engaged.
Referring to
Instead of engaging the ninth rib 26i, the top edge 55a of the anchor member 48 may be configured to engage the wearer 10 just above the bottom of the tenth rib, shown at 26j, and to urge the ribs 26 upwards by that engagement.
The anchor member 48 may be made from any suitable material, and is preferably made from a material with some elasticity to permit it to fit snugly around the wearer 10. A snug fit assists the anchor member 48 in engaging the torso 12 and in resisting riding up on the wearer 10 during use.
Referring to
The straps 50 each have a shoulder-engaging portion 86 which engages one of the shoulder joints 34 (see
Referring to
Referring to
The angle of the rear portion 50b may be selected to be non-vertical. By selecting the angle to be non-vertical, some of the force exerted by the rear strap portion 50b on the shoulder joint 34 (through the shoulder engaging portions 86) is in the medial direction. Thus, the straps 50 are, in such an embodiment, adapted to carry a tensile force that urges the shoulder joints 34 medially.
To facilitate the carrying of tension in the straps 50, the straps 50 may be made from a material that has a selected amount of elasticity, and a selected ratio of elastic tension per unit of stretch. For example, a suitable material may be Supplex™, (ie. the same material as can be used for the anchor portion 48. Another suitable material for the device 48 may be, for example, lingerie-grade Spandex™.
The support device 46 may include a width control device 94 to permit the effective width of the support device 46 to be controlled. This permits control over the tension in the rear strap portions 50b.
Additionally, this permits the support device 46 to accommodate a plurality of wearers 10 having a range of shoulder widths. The width control device 94 may be positioned anywhere suitable, such as on the back 56 of the anchor member 48. The width control device 94 may have any suitable structure. For example, the anchor member 48 may have a separation 96 that extends at least partially down the back 56. The separation 96 may be defined on one side by a first edge 98 of the anchor member 48, and on the other side by a second edge 100 of he anchor member 48. A set of apertures 102 may be provided proximate each edge 98 and 100 of the anchor member 48. A tie member 104 passes through the apertures 102 and is tied to control the size of the separation 96, thereby controlling the distance Ws.
Preferably, the shape of the separation 96, formed by the edges 98 and 100 is a V-shape. A V-shape reduces the amount of bunching that might occur if the edges 98 and 100 were parallel and the separation 96 were generally rectangular.
The width control device 94 in combination with the straps 50 and the back 56 of the anchor member 48 act to adduct the scapulae 22. Additionally, by tightening the width control device 94, the straps 50 will urge the shoulders 15 back further and will further adduct the scapulae 22. Thus the urging force on the scapulae 22 and in turn the amount of adduction can be controlled by means of the width control device 94.
The rearward movement of the shoulder joint 34 (
Additionally, the movement of the clavicles 30 moves the manubrium sternum forward (anteriorly) increasing the distance, or ‘diameter’ between the manubrium sternum and the anterior border of the body of T3 (the third thoracic vertebra), thereby alleviating (at least in some individuals) compression of certain veins, such as the brachiocephalic vein.
Additionally, the rearward movement of the shoulder joint 34 and any medial movement of the shoulder joint 34 adducts the scapula 22 (moves the scapula 22 medially). The movement of the scapula 22 medially, rotates the clavicle 30 about its own axis in a direction that is clockwise from a viewpoint facing the side of the right shoulder of the wearer 10 and counterclockwise from a viewpoint facing the side of the right shoulder of the wearer 10.
Additionally, the resulting medial movement of the scapula 22 elevates the pectoralis minor tendon 47 (
Additionally, the rearward movement of the shoulders 15 urges the spine 24 of the wearer 10 towards its neutral position, shown in
It is optionally possible for the rear portions 50b (
At least one of the ends 76 and 78 of the straps 50 may be removably connected to the anchor member 48 to facilitate the donning and removal of the support device 46. For example, as shown in
Preferably, the effective length of the front portions 50a of the straps 50 can be adjusted. For example, the ends 76 and 78 may be connectable to the anchor member 48 at a plurality of positions, thereby permitting the effective length of the straps 50 to be adjusted. For example, a plurality of sets of eyes 81b may be provided at different distances from the upper edge 55a of the anchor member 48 for receiving the hooks 81a from each of the straps 50. Alternatively, or additionally, a plurality of sets of hooks 81a may be provided at different distances from the second ends 78 of the straps 50. Thus, the effective length of the straps 50 can be adjusted by changing which set of eyes 81b receive the hooks 81a. The hook-and-loop connector portion 82 is connectable regardless of which set of eyes 81b are selected for receiving the hooks 81a.
Alternatively, the effective length of the straps 50 may be made adjustable by any other suitable means. For example, the straps 50 may include a length adjustment buckle, similar to that found on the shoulder straps of backpacks, or similar to that found on a belt.
As a result of the tension carried in the straps 50, some downward force will be exerted on the shoulders 15. The straps 50 avoid exerting any downward force on the clavicles 30 in order to avoid compression of the neurovascular structures 44 in the gap.
The shoulder-engaging portion 86 of each strap 50 has a medial edge, which is shown at 87, and which represents the medial limit to any downward force exerted by each shoulder-engaging portion 86 on the clavicle 30. It can be seen in
For the purposes of clarity, the medial edge 87 referred to above relates to the medial edge of the shoulder-engaging portion 86 only where it is relevant to the potential for compression of the clavicle 30. Therefore, it is not important whether portions of the shoulder-engaging portion 86 that are anterior or posterior to the clavicle 30 lie medially to the acromioclavicular joint 42, since they would not compress the clavicle 30 during use under normal conditions.
By contrast, certain posture support garments of the prior art engage the shoulders 15 medially of the acromioclavicular joints 42 and as a result they exert a downward force on the clavicles 30, which among other things, can result in compression of the underlying neurovascular structures 44 whether or not the shoulders 15 are moved rearward. Additionally, compression of the scalene muscles and the trapezius muscles can occur with some prior art posture support garments, which can cause discomfort or pain for the wearer.
The shoulder-engaging portions 86 may have a generally cupped shape in a front or rear elevation view, for cupping the shoulder joints 34, thereby inhibiting the straps 50 from moving medially on the wearer 10, and from slipping downwards along the arms 14 of the wearer 10. The cupped shape may be formed any suitable way. For example, the cupped shape may be formed by an arm-parallel portion 89 and a shoulder-parallel portion 90, which meet along a seam 92. Alternatively, the cupped shape may be formed in any suitable way.
In the embodiment shown in
The path of each of the straps 50, (ie. passing between the front 54 of the anchor member 48 and the rear 56 of the anchor member 48 over one of the shoulders 15), is such that the straps 50 avoid passing across the anterior axillary fold 95. By avoiding passing across the fold 95, the straps 50 (and the entire support device 46) avoid compression of the lateral edge of the fold 95.
In addition to the above, it will be noted that the posture support device 46 does not include any force-carrying members that encircle the thorax either alone or in combination, thereby facilitating expansion of the rib cage that takes place during breathing by the wearer 10.
Scapular pads may be positioned in the back 56 of the anchor member 48 to enhance correction of scapular ptosis. The scapular pads may be triangular and increase the pressure on the shoulder blade moving them tighter to the back of the chest wall and in toward the midline of the thoracic spine. In one embodiment, they may be arranged such that the base of the triangle is vertical and the apex points toward the spine 24. The base of the triangle may be in the plane of the junction of the back side of the arm 14 and the axilla 93. Depending on the comfort introduced by the compression, thicker or thinner pads can be used. The pads may be made of a variety of materials.
An optional guide strap 105 (
It is optionally possible to include one or more strap fixing members 103 for inhibiting migration of the straps 50 on the wearer 10 during use. For example, the optional guide strap 105 shown in
The strap-to-strap connector 105 is preferably made from a material that has relatively little elasticity, so that it does not apply a force urging the straps 50 towards each other when the device 46 is being worn, so as not to encourage the straps 50 to migrate up towards the neck of the wearer 10. In order to fit wearers 10 having different shoulder widths, the strap-to-strap connector 105, if present could be made to be adjustable in length by some suitable means.
The strap-to-strap connector 105 may substantially cover the entirety of the space between the first and second straps 50 on the front of the support device 46. In other words, the strap-to-strap connector 105 may extend over the space defined by the straps 50, the anchor member 48 and the planned neckline for the wearer 10.
It is optionally possible for the strap-to-strap connector 105 to extend between each strap 50 and some point on the anchor member 48.
As shown in
Referring to
Each sleeve portion 108 includes a wrap-around portion 108a that wraps around an arm 14 of the wearer 10, however, that portion 108a is positioned below the axilla 93 to avoid compression of the anterior axillary fold 95 (
The sleeve wrap-around portion 108a may be provided with a sleeve circumference adjustment device 111 which permits the effective circumference of the sleeve wrap-around portion 108a to be adjusted so that it has sufficient grip on the arm 14 to permit it to retain the shoulder-engaging portions 86 in place, without causing undue discomfort, or pain to the arm 14 and without causing undue compression of any neurovascular structures in the arm 14, particularly those structures on the upper portion of the arm 14 facing the side 27 of the thorax 21, where the arm 14 is relatively sensitive. The sleeve circumference adjustment device 111 may have any suitable structure. For example, it may include one or more hook and loop connectors 113 on the sleeve wrap-around portion 108a. Alternatively, it may include one or more buckles and adjustment straps on each sleeve wrap-around portion 108a.
Reference is made to
It is also optionally possible for the support device 106 to include the connector 60 (
In order to be able to be put on the posture support device 106, the material from which it is made could be selected to have sufficient elasticity to permit the anchor member 48 to be pulled over the head 13 and shoulders 15 of the wearer 10 to its target position on the torso 12 of the wearer 10. Alternatively the device 106 could be made to have sufficient elasticity (through construction from a suitable material) to permit the wearer 10 to step into it and pull it upwards into position.
The optional guide strap 105 and the optional strap fixing member or members 103 (
Reference is made to
The posture support device 109 includes the anchor member 48, the first and second straps 50, and further includes a plurality of covering panels 110. The covering panels 110 are connected to the anchor member 48 and the first and second straps 50 and extend across spaces therebetween to cover portions of the body of the wearer 10 that are not covered by the anchor member 48 or the first and second straps 50.
The covering panels 110 connect to the anchor member 48 and straps 50 in such a way so that they exert substantially no force related to postural support on the wearer 10. In other words, the covering panels 110 cover the body of the wearer 10 without acting as force transfer members, as opposed to the anchor member 48 and the first and second straps 50 which do act as force transfer members and which do exert forces related to postural support on the wearer 10. Preferably, the covering panels 110 exert substantially no forces at all on the wearer 10, however, it is possible that they will exert some force on the wearer 10 in certain circumstances. For example, when the wearer 10 positions his or her arms 14 or body in certain positions, it is possible that the covering panels 110 may exert a force on the body of the wearer 10, however, such a force is not a force associated with posture support. As another example, it is possible that the covering panels will be made to fit relatively snugly against the skin of the wearer 10, however they may be made from a relatively elastic material that stretches easily. As a result of their snug fit and their elasticity, they may exert a small force on the body of the wearer 10 at all times while the support device 109 is worn, however this force is relatively small and is not related to postural support.
The covering panels 110 may be configured in any suitable way to cover the body of the wearer 10. For example, the covering panels 110 may include right and left sleeves 112, right and left side panels 116 (the right side panel 116 is shown in
Each side panel 116 extends along a side 16 of the torso 12 of the wearer 10, connecting between the front portion 50a of a strap 50, the rear portion 50b of the same strap 50 and a side 57 of the anchor portion 48. Each sleeve 112 connects between one of the side panels 116, and also connects to the shoulder-engaging portion 86 of the first strap 50. It is optionally possible for the side panels 116 to connect along the entirely of the outside edges of the first and second straps 50 and for the sleeves 112 to attach entirely to the side panels 116 instead of attaching partially to the first and second straps 50.
The front panel 120 attaches between the first and second straps 50 and attaches at its bottom to the front 54 of the anchor member 48. The front panel 120 extends up to the shoulders 15 of the wearer 10 and forms the front of the neck aperture of the posture support device 109. Depending on the extent of coverage of the back 56 of the anchor portion 48 over the back 18 of the torso 12 of the wearer 10, one or more back panels 122 may be provided which may, for example, connect between the back 56 of the anchor portion 48, the first and second straps 50 and the front panel 120. The back panels 122 may define at least a portion of the back portion of the neck aperture of the support device 109.
The front and back panels 120 and 122 each connect to both straps 50 proximate the shoulders 15. As a result, the front and back panels 120 and 122 each act as strap fixing members.
As shown in
The zipper 126 include a handle 127, which may be provided with a sufficiently long pull-cord to extend over the shoulders to the front of the wearer 10, thereby permitting the wearer 10 to close the zipper 126 by themselves while wearing the support device 109.
As an alternative to a zipper, it is possible for the support device 109 to incorporate a width control device 124 that is similar to that shown for the support device 46 shown in
Reference is made to
It is optionally possible that the front panel 120 would be replaced by the strap-to-strap connector 105. Alternatively, it is optionally possible for the support device 109 to include a strap-to-strap connector 105 that does not cover the entirety of the space between the first and second straps 50, and to further include a front panel 120, to cover the portion or portions of the front of the torso 12 not covered by the strap-to-strap connector 105.
Depending on the purpose of the support device 109, the device 109 may be configured to substantially conceal the fact that it is a posture support device so that it presents to others as simply being a piece of clothing, optionally fashionable clothing. Alternatively, the support device 109 may be configured for use as a sport garment, in which case, it may be more acceptable for it to be visually apparent that the support device 109 is acting as a posture support device and is not simply to cover the body of the wearer 10. Thus, particularly in the case where it is a sport garment, the support device 109 may include openable connectors 60 and/or 80 to facilitate donning and removal.
It is optionally possible for the support device 109 to have as few as one covering panel 110, which covers a single portion of the body of the wearer 10.
In any of the embodiments disclosed herein, it is optionally possible to provide strengthening members, such as, for example, vertically extending semi-rigid bars, at selected positions in the support device. These strengthening members facilitate the transmission of forces throughout some or all of the support device.
For all of the support devices provided above, it is contemplated that several sizes of the device can be provided so that the device can be used by a relatively wider portion of the general population.
The posture support device 46, 106 or 109 can be worn by a male, as shown in
The benefits provided by the posture support devices 46, 106 and 109 shown and described herein may not exist for every individual. However, some individuals will receive at least some of the benefits of the support devices 46, 106 or 109.
The posture support device 46, 106, 109 can be worn 24 hours a day, if desired. For example, with loose clothing, the front circumference adjustment device 67 and the sleeve circumference adjustment devices 111 can be adjusted for comfort or for increased postural stability in situations that create prolonged postural strain such as typing, driving, and in some cases sleeping.
In another aspect of the present invention, a method is provided for selecting, fitting, and ordering a body posture device. The order may be achieved through a variety of methods including but not limited to using a web interface, a telephone, or the like. In one embodiment, the steps may comprise:
1. Determine method of payment once order has appeared in the chartware or other means of notice.
2. In order to obtain authorization from comp: a) use the “click-on” vignettes to illustrate the device and describe its use and b) click on a statement that indicates the specific need that the selected patient has for the device. Fax this with copy of order to the carrier in conjunction with phone request.
3. If Medicare, then use the Medicare billing numbers and submit.
4. If private, fax the order but secure payment before issuing the device.
The ordering process would in one embodiment comprise:
1. Copy “brace measurements” form in documents and click on any explanatory statements that are needed to anticipate or answer the carrier's questions. These will be in a file within the Brace Measurements folder but also may probably be in chartware as a set of snippets justifying the need for the device.
2. Once authorization has been obtained from comp, then fax the order form with measurements including clicking to add any or all of the added features: night yoke, scapular pads, or interscapular bolsters, and if so, which size.
3. Record the required tracking information on the master order list that indicates payer, date of authorization, date order faxed, any tracking number if we agree to use one and later indicate once the completed item comes to us for stock indicating whether it has the appropriate attachments or not.
While the above description constitutes the preferred embodiments, it will be appreciated that the present invention is susceptible to modification and change without departing from the fair meaning of the accompanying claims.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/IB06/01257 | 3/6/2006 | WO | 00 | 8/31/2007 |
Number | Date | Country | |
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60658843 | Mar 2005 | US |