Systems and methods for monitoring a subject's effective use of a self-contained portable positionable oscillating motor array
In some embodiments, a method may include monitoring use of a medical device. The method may include positioning a wearable harness of a medical device on a subject. The method may include selectively positioning at least some of a plurality of engines on and/or adjacent at least one treatment area. The method may include applying an oscillation force to at least one of the treatment areas using at least some of the engines. The method may include mobilizing at least some secretions in an airway within the subject substantially adjacent the treatment areas. The method may include monitoring use of the medical device by the subject using a controller associated with the medical device to determine if the medical device has been used effectively as prescribed.
1. A method of monitoring use of a medical device, comprising:
positioning a wearable harness of a medical device on a torso of a subject;
applying an oscillation force to at least one treatment area using at least some of a plurality of engines coupled to the wearable harness;
mobilizing at least some secretions in an airway within the subject substantially adjacent the treatment areas; and
monitoring use of the medical device by the subject using a controller associated with the medical device, wherein monitoring use of the medical device includes monitoring for activation of the medical device while the subject wears the medical device, and wherein monitoring for activation includes:
assessing a voltage drawn by the at least some of the plurality of engines using the controller; and
determining, by the controller, the medical device has been activated while the subject wears the medical device for a period of time based on assessing an increase in the voltage drawn by the at least some of the plurality of engines for the period of time.
2. The method of claim 1 , wherein determining the medical device has been activated while the subject wears the medical device for a period of time provides a confirmation that the subject has worn the medical device and applied the oscillation force while wearing the medical device.
3. The method of claim 1 , wherein monitoring use of the medical device by the subject includes determining whether the medical device has been used effectively by determining whether the increase in the voltage drawn by the at least some of the plurality of engines for the period of time is in a range of voltage corresponding to correct compression for the medical device.
4. The method of claim 1 , further comprising selectively positioning at least some of a plurality of engines at least adjacent to at least one treatment area, wherein at least one of the plurality of engines is releasably couplable to the wearable harness such that at least one of the plurality of engines is positionable relative to the subject using a positioning system.
5. The method of claim 1 , wherein monitoring use of the medical device includes monitoring a change in vibration of the at least some of the plurality of engines to determine whether compression has been applied to the at least some of the plurality of engines while said engines are on.
6. The method of claim 1 , wherein monitoring use of the medical device includes monitoring a change in vibration of the at least some of the plurality of engines using a vibration sensor to determine whether compression has been applied to the at least some of the plurality of engines while said engines are on.
7. The method of claim 1 , wherein monitoring use of the medical device comprises monitoring a change in acceleration of the at least some of the plurality of engines to determine whether compression has been applied to the at least some of the plurality of engines while said engines are on.
8. The method of claim 1 , wherein monitoring use of the medical device comprises monitoring a change in acceleration of the at least some of the plurality of engines using an acceleration sensor to determine whether compression has been applied to the at least some of the plurality or engines while said engines are on.
9. The method of claim 1 , further comprising notifying, using a wireless connection to the controller, a care provider as to whether or not the subject is complying with a prescription associated with the medical device.
10. The method of claim 1 , further comprising notifying a care provider as to whether or not the subject is complying with a prescription associated with the medical device.
11. The method of claim 1 , further comprising notifying a care provider as to whether or not the subject is complying with a prescription associated with the medical device, wherein the prescription has been input in the controller.
12. The method of claim 1 , wherein the wearable harness includes an inner wearable harness and an outer wearable harness, and wherein positioning the wearable harness or the medical device on the torso of the subject includes:
positioning the inner wearable harness on the torso of the subject;
positioning the outer wearable harness on the torso of the subject; and
applying an oscillation force to at least one of the treatment areas using the at least some of the plurality of engines.
13. The method of claim 12 , further comprising providing a compressive force to at least some of the activated plurality of engines to the treatment area by activating the outer wearable harness.
14. The method of claim 13 , wherein monitoring use of the medical device by the subject includes determining whether the compressive force has been applied effectively based on the voltage drawn by the at least some of the plurality of engines for the period of time being in a range of voltage corresponding to correct compression for the medical device.
15. The method of claim 13 , wherein monitoring use of the medical device by the subject includes determining whether the compressive force has been applied within a prescribed range based on the voltage drawn by the at least some of the plurality of engines for the period of time being in a range of voltage corresponding to correct compression for the medical device.
16. The method of claim 1 , further comprising assessing treatment areas of the subject's chest for placement of at least some of a plurality of the engines coupled to the wearable harness, such that the at least some of the plurality of engines are at least adjacent treatment areas that need secretion mobilization.
17. A system, comprising:
a wearable harness worn, during use, on a torso of a subject, wherein the wearable harness comprises a compression mechanism having an activation mechanism;
a plurality of engines which when activated apply an oscillation force to at least one treatment area of the subject, wherein at least one of the plurality of engines is releasably couplable to the wearable harness such that at least one of the plurality of engines is selectively positionable relative to the subject using a positioning system, wherein the positioning system allows positioning at least one of the plurality of engines such that the oscillation force is applied to at least one of the treatment areas of the subject, and wherein the oscillation force mobilizes, during use, at least some secretions in an airway within the subject at least adjacent the treatment area;
at least one sensor coupled to the wearable harness, wherein the at least one sensor is configured to sense at least one physical property of the wearable harness; and
a controller coupled to the plurality of engines and the at least one sensor, wherein the controller is configured to control operation of the plurality of engines, and wherein the controller is configured to assess usage of she wearable harness and the plurality of engines based on a voltage drawn by the plurality of engines and the sensed at least one physical property of the wearable harness;
wherein the compression mechanism adjusts the oscillation force applied by at least some of the activated plurality of engines to the treatment area; and
wherein the activation mechanism of the compression mechanism is positioned along a longitudinal length of the wearable harness along a left or right side of a user during use.
18. The system of claim 17 , wherein the compression mechanism tightens at least a portion of the wearable harness against the torso of the subject such that the oscillation force applied by the at least some of the activated plurality of engines to the treatment area is adjusted.
19. The system of claim 17 , wherein the compression mechanism comprises at least one set of lacing along a longitudinal length of the wearable harness.
20. The system of claim 17 , wherein the compression mechanism comprises at least one set of buckles along a longitudinal length of the wearable harness.
21. The system of claim 17 , wherein the compression mechanism comprises at least one set of ratcheting buckles along a longitudinal length of the wearable harness.
22. The system of claim 17 , wherein the compression mechanism is positioned along a longitudinal length of the wearable harness along a left or right side of a user during use.