PATIENT BEHAVIOR MONITORING

1 . A method for assessing treatment of a subject who has overactive bladder (OAB), the method comprising:

using an implant, stimulating a tibial nerve of the subject according to a stimulation protocol; and

using an electronic processor:

receiving data from one or more sensors, the data being indicative of activity of the subject over a time period extending over at least one week, and

based on the data, assessing a characteristic of a response of the subject to the stimulation.

2 . The method according to claim 1 , wherein receiving the data comprises receiving data not indicative of a frequency of specific voiding episodes of the subject.

3 . (canceled)

4 . The method according to claim 1 , wherein receiving the data comprises receiving data indicative of a cumulative duration of time during which the subject is not at home.

5 . The method according to claim 1 , wherein receiving the data comprises receiving data indicative of a cumulative duration of time during which the subject is not in a workplace of the subject.

6 . The method according to claim 1 , wherein receiving the data comprises receiving data indicative of a cumulative duration of time during which the subject is not indoors.

7 . The method according to claim 1 , wherein receiving the data comprises receiving data indicative of a cumulative duration of a plurality of periods of motion of the subject.

8 - 9 . (canceled)

10 . The method according to claim 1 , further comprising outputting to the subject an indication of the assessment.

11 . The method according to claim 1 , further comprising, responsively to the assessment, outputting to the subject a modification of the stimulation protocol.

12 . (canceled)

13 . The method according to claim 1 , wherein receiving the data comprises receiving data indicative of a level of physical activity of the subject.

14 - 16 . (canceled)

17 . The method according to claim 13 , wherein receiving the data comprises receiving smartphone-derived data.

18 - 22 . (canceled)

23 . The method according to claim 1 , wherein receiving the data comprises receiving the data from the one or more sensors:

prior to a first time that the tibial nerve is stimulated using the implant, and

subsequently to the first time that the tibial nerve is stimulated using the implant.

24 - 27 . (canceled)

28 . The method according to claim 1 , wherein receiving data from the one or more sensors comprises receiving data indicative of a distance traveled by the subject.

29 - 30 . (canceled)

31 . The method according to claim 28 , wherein receiving the data indicative of the distance traveled comprises receiving GPS-derived data.

32 . The method according to claim 28 , wherein assessing the characteristic of the response of the subject to the stimulation based on the data comprises identifying a positive result of the stimulation based at least in part on a post-treatment-initiation distance traveled by the subject subsequently to the first time that the tibial nerve is stimulated using the implant being greater than a predetermined threshold distance during a given time period.

33 - 38 . (canceled)

39 . The method according to claim 1 , further comprising, based on the data, calculating a quality-of-life score indicative of a level of recovery of the subject from OAB.

40 - 42 . (canceled)

43 . The method according to claim 1 , wherein:

the time period is a first time period,

the stimulation protocol is a first stimulation protocol,

the step of assessing comprises assessing the characteristic of the response of the subject to the stimulation over the first time period, and the method further comprises:

responsively to the step of assessing, determining a second stimulation protocol,

using the implant, stimulating the tibial nerve according to the second stimulation protocol over a second time period extending over at least one week,

using the electronic processor, receiving a second set of data from the one or more sensors, the data being indicative of activity of the subject over the second time period, and

based on the second set of data, assessing the characteristic of the response of the subject to the stimulation over the second time period.

44 . The method according to claim 43 , wherein:

stimulating the tibial nerve according to the first stimulation protocol comprises stimulating the tibial nerve during a first number of daily stimulation sessions, and

the step of stimulating the tibial nerve according to the second stimulation protocol comprises stimulating the tibial nerve during a second number of daily stimulation sessions.

45 . (canceled)

46 . The method according to claim 43 , wherein determining the second stimulation protocol comprises determining a change in a parameter of internal operation of the implant.

47 . The method according to claim 46 , wherein:

stimulating the tibial nerve according to the first stimulation protocol comprises stimulating the tibial nerve at a first amplitude of individual current pulses,

determining the change in the parameter comprises determining a change in the amplitude of individual current pulses, and

the step of stimulating the tibial nerve according to the second stimulation protocol comprises stimulating the tibial nerve at a second amplitude of individual current pulses.

48 . The method according to claim 46 , wherein:

stimulating the tibial nerve according to the first stimulation protocol comprises stimulating the tibial nerve at a first pulse frequency of applied current,

determining the change in the parameter comprises determining a change in the pulse frequency of applied current, and

the step of stimulating the tibial nerve according to the second stimulation protocol comprises stimulating the tibial nerve at a second pulse frequency of applied current.

49 - 67 . (canceled)