Extracorporeal devices and methods for facilitating cessation of undesired behaviors

• US 9,675,275 B2
• Filed: 10/22/2010
• Issued: 06/13/2017
• Est. Priority Date: 10/24/2009
• Status: Active Grant

• Current Assignee: Pivot Health Technologies Incorporated
• Original Assignee: Carrot Sense, Inc.
• Inventors: Utley, Haley Grace, Utley, MacKenzie Taylor, Utley, Emma Kathryn, Utley, David Scott, Utley, Jack Denton, Utley, Kathryn Mary, Utley, Alek Denton
• Primary Examiner(s): Jackson, Gary
• Assistant Examiner(s): Nganga, Boniface N
• Application Number:
  US12/910,371
• Publication Number:
  US 20110263947A1
• Time in Patent Office: 2,426 Days
• Field of Search: 607900
• CPC Class Codes: A61B 5/082 Evaluation by breath analysis, e.g. determination of the chemical composition of exhaled breath A61B5/083, A61B5/091 take precedence
• CPC Class Codes: A61B 5/4845 Toxicology, e.g. by detection of alcohol, drug or toxic products A61B5/4848 takes precedence

Abstract

Devices, Methods and Systems are disclosed for assisting patients in behavioral modification and cessation programs aimed at terminating undesired behaviors such as smoking, alcohol use and others. Patient devices with automated patient prompting for self-testing, analysis of test results and data logging are included in a networked system with a specifically designed treatment modality.

Claims

1. A system for facilitating cessation of undesired behavior in a patient, comprising:

a module containing at least instructions comprising a predetermined test protocol, the test protocol including a number and timing of patient testing prompts;

a patient device (PD) configured and dimensioned to be carried by the patient, the patient device comprising;

a PD user interface,

a test element configured to receive a biological input from the patient and output information representative of the content of the biological input,

a PD storage module containing at least instructions for prompting the patient through the PD user interface to provide a biological input to the test element at selected intervals corresponding to the predetermined test protocol, the PD storage module further containing instructions for receiving from the patient through the PD user interface a non-biological lifestyle input relating to the patient,

wherein the PD is configured for determining the completeness of the biological input, and providing additional patient prompts based on said completeness determination; and

a PD execution module communicating with the PD user interface, the test element and the storage module, the PD execution module configured to execute instructions contained in said PD storage module; and

a health care provider device (HCPD) configured to be accessed by a health care provider, comprising;

an HCPD user interface,

a HCPD storage module containing at least instructions for displaying and manipulating information representative of the content of the biological input, the HCPD storage module further containing instructions for associating the non-biological lifestyle input with the content of the biological input that is closest in time to the non-biological lifestyle input,

wherein the HCPD is further configured for evaluating the predetermined test protocol including the number and timing of patient test prompts based on at least one of user input and said information representative of the content of the biological input, where an evaluation comprises categorizing the biological input and non-biological lifestyle input as either negative or positive for smoking behavior relative to a predetermined threshold, and

wherein the HCPD is further configured for altering or maintaining the predetermined test protocol based on said evaluation of a negative or positive determination for smoking behavior; and

an HCRD execution module communicating with the HCPD user interface and HCPD storage module, the execution module configured to execute instructions contained in said HCPD storage module,

wherein said PD and HCPD are configured for communication there between.

2. The system of claim 1, wherein one of the PD or HCPD storage modules contains instructions for generating a machine readable data set based on said test element output information, and for associating said data set with a specific patient biological input.

3. The system of claim 2, wherein one of the PD or HCPD storage module contains instructions for causing the patient device to prompt the patient to input requested information to said patient device through the PD user input and for associating the requested information with a data set associated with a specific patient biological input.

4. The system of claim 1, wherein the test element comprises a detector configured to detect substances in exhaled breath.

5. The system of claim 1, wherein the test element comprises a detector configured to detect substances in saliva.

6. The system of claim 1, wherein the patient device and healthcare provider device are configured for communication through a network.

7. The system of claim 6, wherein the network is a telephone network.

8. The system of claim 6, wherein the network is a computer network.

9. The system of claim 6, wherein the network is the Internet.

10. The system of claim 1, wherein the patient device and health care provider device are configured for communication through a transferrable storage medium.

11. The system of claim 1, wherein the patient device and health care provider device are configured for communication through a direct wired connection.

12. The system of claim 1, further comprising plural said patient devices configured to communicate with at least one said health care provider device.

13. The system of claim 1, wherein the PD storage module further includes instructions for delaying said determining the completeness of the biological input for a set period in response to a patient input through the PD user interface.

14. The system of claim 1, wherein:

the patient device is contained within a housing;

the patient device further comprises an identification device for acquiring patient identifying information correlated to the biological input; and

said identification device communicating with said storage module and execution module for associating the acquired identifying information with the correlated biological input and storing said associated identifying information.

15. The system of claim 1, wherein the PD storage module further includes instructions for receiving unprompted patient input through the PD user interface and for associating said unprompted input with the biological input based on a predetermined algorithm.

16. The system of claim 1, wherein said patient device is contained within a housing.

17. The system of claim 1, wherein said patient device comprises at least two housings, with the test element disposed in one housing and the PD user interface disposed in a separate housing, and wherein said test element and PD user interface are configured for wireless communication there between.

18. The system of claim 1, wherein said test element is configured for detecting one or more substances associated with smoking tobacco products.

19. The system of claim 1, wherein said test element is configured for detecting one or more substances associated with smoking of illegal drugs.

20. The system of claim 1, wherein said test element is configured for detecting alcohol.

21. The system of claim 1, wherein the test element is configured for detecting substances associated with oral ingestion or transdermal absorption of specified compounds.

22. The system of claim 21, wherein said specified compounds include one of molecules related to benzodiazepines, narcotics, LSD, GHB, Rohypnol, ketamine, methamphetamine, PCP/phencyclidine, anabolic steroids, and secreted or exhaled metabolites of said substances.

23. The system of claim 1, wherein the test element is configured for detecting one or more substances associated with oral placement of products.

24. The system of claim 1, wherein the test element is configured for detecting one or more substances associated with nasal sniffing of substances of abuse.

25. The system of claim 1, wherein the module containing the instructions comprising the predetermined test protocol is disposed within the PD storage module.

26. The system of claim 1, wherein the module containing the instructions comprising the predetermined test protocol is disposed within the HCPD storage module.

27. The system of claim 1, wherein the predetermined test protocol further includes prompting the patient to input information regarding patient life events associated with select test protocol events.

28. An apparatus for use in connection with facilitating cessation of undesired behavior in a patient, comprising:

at least one housing configured and dimensioned to be carried by the patient;

a user interface disposed in said at least one housing;

a test element disposed in said at least one housing, the test element being configured to receive a biological input from the patient and output information representative of the content of the biological input,

a storage module containing instructions comprising;

a) executing a predetermined test protocol including a number and timing of patient test prompts, said protocol further comprising;

prompting the patient through the user interface to provide a biological input to the test element at selected intervals corresponding to the number and timing of patient test prompts,

determining the completeness of a biological input,

providing additional patient biological input prompts based on said completeness determination,

prompting the patient to input requested information through said user interface, and

receiving from the patient through the user interface a non-biological lifestyle input relating to the patient,

b) generating user readable indicator based on said test element output and displaying said output on the user interface,

c) associating the user readable indicator with a specific biological input,

d) associating the requested information with a specific user readable indicator associated with a specific patient biological input,

e) associating the non-biological lifestyle input with the specific biological input that is closest in time to the non-biological lifestyle input,

f) storing test result information including the user readable indicator and associated requested information in said storage module, and

g) evaluating the predetermined test protocol by categorizing the biological input and non-biological lifestyle input with either a negative or positive for smoking behavior relative to a predetermined threshold; and

an execution module communicating with the user interface, the test element and the storage module, the execution module configured to execute said instructions,

wherein said apparatus is configured to communicate through a network for transfer of said test result information and to receive instructions for altering the predetermined test protocol based on a remote evaluation of said test result information.

29. The apparatus of claim 28, wherein the storage module further includes instructions for delaying said determining the completeness of biological input for a set period in response to a patient input through the user interface.

30. The apparatus of claim 29, further comprising an identification device for acquiring patient identifying information correlated to a biological input, said identification device communicating with said storage module and execution module for associating the acquired identifying information with the correlated biological input and storing said associated identifying information.

31. The apparatus of claim 30, wherein said apparatus comprises a single housing.

32. The apparatus of claim 28, wherein said apparatus comprises two housings with the test element disposed in a first housing and said user interface, storage module and execution module disposed in a second housing, said test element and execution module being configured for wireless communication there between.

33. An apparatus for use in connection with facilitating cessation of undesired behavior in a patient, comprising:

a housing configured and dimensioned to be carried by the patient;

a user interface disposed in said housing, the user interface configured to prompt the patient;

a test element disposed in said housing, the test element being configured to receive a biological input from the patient and output information representative of the content of the biological input;

a patient identification module disposed in said housing configured to recognize a unique characteristic of the patient;

at least one storage module disposed in said housing containing instructions comprising;

a) instructions for executing a predetermined test protocol, the test protocol including a pre-determined number and timing of patient test prompts, the instructions including,

prompting the patient through the user interface to provide a biological input to the test element at selected intervals in accordance with the test protocol,

determining the completeness of a biological input,

providing additional patient biological input prompts based on said completeness determination,

prompting the patient to input requested information through said user interface, and

receiving from the patient through the user interface a non-biological lifestyle input relating to the patient,

b) instructions for generating user readable indicator based on said test element output and displaying said output on the user interface,

c) instructions for associating the test element output with a specific biological input,

d) instructions for associating any requested information with a specific test element output associated with a specific patient biological input,

e) instructions for associating the non-biological lifestyle input with the specific biological input that is closest in time to the non-biological lifestyle input,

f) instructions for initiating the patient identification module correlated to said prompting and re-prompting upon determination of an unrecognized patient characteristic, and

g) instructions for evaluating the predetermined test protocol by categorizing the biological input and non-biological lifestyle input with either a negative or positive for smoking behavior relative to a predetermined threshold; and

an execution module communicating with the user interface, the test element, the storage module and the patient identification module, the execution module configured to execute said instructions,

wherein said apparatus is configured to communicate through a network.

34. The apparatus of claim 33, wherein the storage module further contains instructions comprising:

g) evaluating the predetermined test protocol based on said test result information; and

h) altering or maintaining the predetermined test protocol based on said evaluation, said altering including changing at least one of the predetermined number or timing of patient test prompts.

35. The apparatus of claim 33, wherein the storage module further contains instructions for altering the predetermined test protocol including changing at least one of the predetermined number or timing of patient test prompts in response to an altering instruction received through the communication network.

36. The apparatus of claim 33, wherein said apparatus is configured to receive the predetermined test protocol through said network communication.

37. The apparatus of claim 33, wherein the instructions prompting the patient for requested information includes instructions prompting the patient to input information through the user interface identifying patient activity at the time of the test prompt.

38. An apparatus for use in connection with facilitating cessation of undesired behavior in a patient, comprising:

a housing configured and dimensioned to be carried by the patient;

a graphical user interface disposed in said housing, said interface configured to prompt the patient and receive informational inputs by the patient;

a test element disposed in said housing, the test element being configured to receive a biological input from the patient and output information representative of the content of the biological input,

a storage module within said housing containing instructions comprising instructions for;

a) executing a predetermined test protocol including a number and timing of patient test prompts, said protocol further comprising

prompting the patient through the user interface to provide a biological input to the test element at selected intervals corresponding to the number and timing of patient test prompts,

determining the completeness of a biological input,

providing additional patient biological input prompts based on said completeness determination, and

receiving from the patient through the user interface a non-biological lifestyle input relating to the patient,

b) generating user readable indicator based on said test element output and displaying said output on the graphical user interface,

c) associating the test element output with a specific biological input,

d) associating the non-biological lifestyle input with the specific biological input that is closest in time to the non-biological lifestyle input,

e) transferring said test result information including the test element output associated with a specific biological input to a network or storage device;

f) receiving instructions for altering the predetermined test protocol based on a remote evaluation of said test result information, and

g) evaluating the predetermined test protocol by categorizing the biological input and non-biological lifestyle input with either a negative or positive for smoking behavior relative to a predetermined threshold, and

an execution module within said housing communicating with the graphical user interface,

the test element and the storage module, the execution module configured to execute said instructions.

39. The apparatus of claim 38, wherein the storage module further includes instructions for delaying said determining the completeness of biological input for a set period in response to an patient input through the user interface.

40. The apparatus of claim 38, further comprising an identification device disposed in said housing for acquiring patient identifying information correlated to a biological input, said identification device communicating with said storage module and execution module for associating the acquired identifying information with the correlated biological input.

41. The apparatus of claim 38, wherein said apparatus is adapted for use in a smoking cessation treatment program and said test element is configured to detect the presence of a marker indicating smoking behavior.

42. The apparatus of claim 38, wherein said apparatus is configured to communicate with a remote station through at least one of a wireless or cellular network, removable storage device or wired connection for said transfer of test result information and said receipt of instructions.

43. The apparatus of claim 38, wherein said instructions further comprise instructions for associating informational inputs through the graphical user interface with specific patient biological inputs, and transferring said associated informational inputs with said test result information.