1. Field of the Disclosure
The present disclosure generally relates to a system for sensing and alerting a user to pressure and force on his foot.
2. Description of the Related Art
Diabetics and other afflicted people with medical problems can have failures in the nervous system. This could be detrimental to their health since they often do not recognize pain, discomfort, irritation, changes in pressure, swelling, changes in temperature or have an inability to recognize pain, discomfort, irritation, changes in pressure, swelling, or changes in temperature to a sufficient degree to prevent injury, or illness to themselves. This is especially prevalent in the feet of the afflicted person with failure(s) in their nervous system since their feet are susceptible to increased pressure, irritation, changes in pressure, swelling, or changes in temperature while standing, sitting or lying down. Thus, an afflicted person may place too much pressure on a foot or a portion of a foot by physical activity, by standing or even while sitting or lying down. This is problematic because too much pressure on the foot or a portion of the foot could cause increased nerve damage to the foot, destruction of the skin creating an open wound, or a host of other ailments. Thus, there is a need for a low-cost system to alert the user to problematic pressure, and other physiologic and biomechanical changes to their foot or feet along with continuous active monitoring of the changes in pressure and other physiologic and biomechanical changes being applied to their foot or feet.
The present invention is a system for sensing and alerting a user to changes in pressure and force upon a foot during resting, sitting , standing or exercise, like walking, by using footwear having a plurality of primary pressure sensors, a medical node connected to the plurality of primary pressure sensors, and a base station connected to the medical node.
The exact nature of this invention as well as other objects and advantages thereof will be readily apparent from consideration of the following specification in conjunction with the accompanying drawings in which like numerals designate like parts through the figures thereof and wherein:
Pressure sensors 8 may be resistive pressure sensors, but are not limited to resistive pressure sensors and can be a variety of other types of pressure sensors as well as other physiological and biomechanical sensors. In either case, medical node 6 receives raw data from pressure sensors 8 and generates pressure data for transmission to a first base station 10 (
Medical node 6 can be, for example, a MediSens MedNode™. Medical node 6 has a transmitter (not shown) and a microprocessor (not shown). The microprocessor allows the medical node 6 to process the raw data from pressure sensors 8 to generate the pressure data. The transmitter is used to transmit the pressure data to the first base station 10.
If footwear 4 is a shoe, a sandal, or a boot, medical node 6 and sensors 8 do not need to be in the general area where the foot applies pressure on pressure sensors 8. For example, medical node 6 and sensors 8 could be in the tongue of the shoe, or on the straps of a sandal, or in the walls and lining of a boot or shoe.
In operation, Pressure sensors 8 sense pressure from a foot placed on them. Where pressure sensors 8 are resistive sensors, the resistance in primary pressure sensors 8 varies as different pressure and/or force is applied to them. Medical node 6 sends current through pressure sensors 8 and determines the pressure at each pressure sensor 8 from the resistance detected.
The secondary pressure sensors 8b could be less expensive than the primary pressure sensor 8a. Secondary pressure sensors 8b could also remain dormant and only be active when activated so as to not unnecessarily draw power. Although
It is also contemplated that some or all of the secondary pressure sensors 8b could be activated even when primary pressure sensor 8a has not failed or is not defective. This could be beneficial when more pressure data is necessary such as when fine analysis is required for pressure on the foot.
As shown in
Instead of or in addition to medical node 6, first base station 10 and/or second base station 20 could also determine if primary pressure sensor 8a is defective or has failed as shown in
Secondary pressure sensor 8b could be cheaper to manufacture, obtain, and/or implement than primary pressure sensor 8a. Secondary pressure sensors 8b could also remain dormant and only be active when activated so as to not unnecessarily draw power from battery 24. Although
It is also contemplated that some or all of the secondary pressure sensors 8b could also be activated even when primary pressure sensor 8a has not failed or is not defective. This could be beneficial when more pressure data is necessary such as when fine analysis is used for the pressure on his foot.
System 2 has a footwear 4 such as one illustrated in
Battery 24 preferably has a minimized physical presence and weight. Battery 24 can be a rechargeable and removable battery. In the situation where battery 24 is a rechargeable and removable battery, medical node 6 can detect when battery 24 is low on power such that it needs to be removed and recharged. Furthermore, battery 24 can also be recharged through the movements of footwear 4 such as when footwear 4 is inserted in a shoe or is a shoe itself. In such a situation it is unnecessary for battery 24 to be removable. Although not shown, a back-up battery can also be included.
First base station 10 is connected to footwear 4 by a connection 14. Connection 14 is a wireless connection in
First base station 10 is a computer, but it can also be any other type of electronic device such as a mobile phone, a blackberry, an iPhone, an iPod, etc. First base station 10 can also be an intermediate communication module such as a monitoring station designed to receive and transmit pressure data which allows the medical node 6 to only transmit pressure data to first base station 10. If first base station 10 is an intermediate communication module, it may have a more powerful transmitter to relay the pressure data to a more distant location to a second base station 20. Battery 24 connected to medical node 6 may thus be reduced in size, reducing costs, and allowing for a greater degree of portability of footwear 4.
First base station 10 can also have a storage device 26 to store the pressure data from the medical node 6. First base station 10 can then use and/or analyze the pressure data to generate useful analysis of the pressure data in the form of X-Y charts based on time and pressure. For example, this could be helpful in detecting problems the user has with placing pressure on his feet and allowing the user to correct such problems.
Furthermore, first base station 10 could also have an optional display 30 as shown in
A second base station 20 may be connected to the first base station 10 by a connection 22. Second base station 20 is preferably a computer. It can also be any other type of electronic device such as a mobile phone, a blackberry, an iPhone, an iPod, etc. Second base station 20 may be located remotely from first base station 10. The user of first base station 10 need not be the same as the user for the second base station 20. The user of the second base station 20 could be a doctor, physician, nurse, or family member, for example. This allows different people to access the pressure data generated by medical node 6.
In operation, foot 12 from a user is placed over footwear 4. The foot 12 applies pressure to footwear 4 through physical contact 18 with the pressure sensor, such as when the user steps on footwear 4. Pressure sensors 8 (8a and/or 8b) detect the pressure being applied by foot 12 and transmit the raw data to medical node 6. Medical node 6 receives the raw data from pressure sensors 8 (8a and/or 8b) through connection 16 and generates pressure data from the raw data.
Medical node 6 transmits the pressure data to a first base station 10 through connection 14. First base station 10 receives the pressure data from medical node 6 and analyzes the pressure data. First base station 10 can also optionally transmit the pressure data to second base station 20 through connection 22.
When first base station 10 analyzes the pressure data, it may generate an event alert if a predetermined event occurs. A predetermined event occurs when the pressure data indicates that there is pressure above a predetermined level and for longer than a predetermined time period at one or more of the primary pressure sensors. This potentially prevents a user from putting too much pressure on a certain portion of his foot 12, preventing the user from cutting off circulation to a portion of his foot and/or destroying the skin and other surrounding tissue structures of the foot. The present invention is designed to help prevent serious damage to a foot structure leading to possible amputation of his foot or afflicted extremity.
When first base station 10 generates an event alert, it sends a text message, page, voice mail or e-mail to the user. First base station 10 can also send auditory signals in addition to other visual or vibratory signals to the user.
As shown in
Display 30 also indicates the user's information such as his ID number, age, height, weight, etc. It also has a section 34 to allow the user to input his phone numbers and/or check to see if the user wants to automatically send a text message, or other alert media if there is a predetermined event. Section 34 of display 30 can also be used to input multiple phone numbers such as the mobile phone number of a doctor or family member. Section 34 may also be used to input a user's e-mail address or other e-mail addresses in which case first base station 10 can automatically send an e-mail to the appropriate person when there is a predetermined event. Section 34 may also be used to generate event alerts to a variety of other devices such as a personal digital assistant, iPod, or other handheld or worn electronic device when a predetermined event occurs.
First base station 10 may also be used to alter the functionality of medical node 6 and pressure sensors 8 (8a and/or 8b). For example, the following alterations to medical node 6 can be performed:
When first base station 10 is communicating with medical node 6 to retrieve data or calibrate medical node 6, first base station 10 and medical node 6 can communicate with a level of security. While it is important to protect medical data, it is also important to minimize cost and realize the limitations of battery 24. Thus, first base station 10 can choose the sophistication of the security used when communicating with medical node 6.
For example, if there are four levels of security possible, with the first security level being the lowest form of security and the fourth security level being the highest form of security, if the situation is urgent, first base station 10 could choose the first security level or lowest form of security. However, if the situation is not urgent, first base station 10 could choose the fourth security level or the highest form of security. A non-urgent situation could be when the user is walking around performing ordinary daily tasks. In that case, the desired security level would be high since the user would want to protect his medical data but has no pressing need to retrieve the pressure data as soon as possible. An urgent situation could be when there is a predetermined event that requires immediate attention. In that case, the desired security level would be minimal since although the user would want to have some form of protection for his medical data, the need to retrieve the pressure data and act on it as soon as possible is more important.
In one contemplated embodiment, the first level of security is plaintext. The second level of security would be authentication only and a type of cipher block chaining would compute and verify the message integrity. The third level of security would have authentication and encryption with Skipjack cryptography. The fourth level of security would have authentication and encryption with RC5 cryptography. It is contemplated that the authentication and encryption necessary for each level of security is changeable as well as having more or less levels of security.
The components of the present invention including first base station 10, second base station 20, medical node 6, and/or primary pressure sensors 8 (8a and/or 8b) can be calibrated. To calibrate the present invention, two types of pressure data are used. First is the amount of whole pressure applied to a foot. Second is the pressure sensed at designated points of the foot such as points where the foot touches the shoe or ground. The pressures sensed can be a variety of types of forces such as shear force. This pressure data will be used to measure and assess the correct pressure. When the user uses footwear 4 for the first time, the present invention will calibrate and get the initial and balanced condition's pressure such as designated points of the foot and the whole foot.
The total pressure sensed from both feet in the calibration state will be used as a parameter for comparison purposes in the future detection of pressure on the foot. In those instances where only one foot is involved parameters for comparison will be derived from the average norm of similar patients with the same condition, as well as from the patient's previous calibrated states. When the calibration is done, the present invention will consistently receive the data from medical node 6, compute the pressure and report the possible percussions based on the following:
1.) Patient is not moving: In this case the present invention will take the whole pressure sensed from both feet. By comparing the relation between the amount of total pressure applied by each foot, or the average norm in the case of one foot, and the pressure active area with the calibrated data, the present invention can detect if the foot with the higher pressure is projecting the correct amount of pressure or not, or if both feet (or foot) are being subjected to excessive pressure as in the case of excessive lower extremity edema. For example if the user is leaning to the left, he puts all of his weights on the left foot while the right foot is still on the ground. In this case the amount of pressure applied to the right foot will be less than normal but the active area is unchanged. However the left medical node will sense more pressure and the active area will be focused in the outer side of the foot. In this case the present invention will compute the pressure based on active area in each shoe and will compare the results with the calibration result. It will then make a decision, such as whether a predetermined event has occurred, based on the comparison.
2) Patient is moving: Movement can be detected as extreme changes in the locality of the pressure applied in foot. For example, pressure will be from the right foot to left foot and from the heel to the toe. The present invention will analyze the data in fixed time intervals. In each time interval the present invention will analyze pressure data received from each footwear 4 similar to when the patient is not moving and first places the footwear 4 or shoe on.
Furthermore, calibration can also be done automatically on medical node 6 each time the shoelace tightness is altered or other events which might alter the analysis of pressure data. Also, since the detected pressure is a function of human mass and the area where the force is applied, the present invention can also be used for measuring the user's weight.
As shown in
Although not shown, footwear 4 could also have temperature sensors connected to medical node 6 to ascertain the temperature of a foot. Alternatively, the pressures sensors 8 (8a and/or 8b) could be configured to sense temperature, too. In addition, footwear 4 could have sensors for the heart rate of a user, galvanic skin response, precipitation, or oximetry, for example. Footwear 4 could also contain an accelerometer.
Obviously many modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be understood that within the scope of the appended claims the invention may be practiced otherwise than as specifically described.
This application claims the benefit of U.S. Provisional Patent Application No. 60/864,050 filed on Nov. 2, 2006, entitled “PRESSURE ALERT SENSING SYSTEM” which is expressly incorporated herein in its entirety.
Number | Date | Country | |
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60864050 | Nov 2006 | US |