Prosecution Insights
Last updated: October 04, 2026
Application No. 18/687,788

BIOFEEDBACK COGNITIVE BEHAVIORAL THERAPY FOR INSOMNIA

Final Rejection §101§103
Filed
Feb 28, 2024
Priority
Aug 30, 2021 — provisional 63/238,437 +1 more
Examiner
NG, JONATHAN K
Art Unit
3619
Tech Center
3600 — Transportation & Electronic Commerce
Assignee
ResMed
OA Round
2 (Final)
36%
Grant Probability
At Risk
3-4
OA Rounds
1y 3m
Est. Remaining
50%
With Interview

Examiner Intelligence

Grants only 36% of cases
36%
Career Allowance Rate
118 granted / 331 resolved
-16.4% vs TC avg
Moderate +14% lift
Without
With
+14.0%
Interview Lift
resolved cases with interview
Typical timeline
3y 10m
Avg Prosecution
32 currently pending
Career history
361
Total Applications
across all art units

Statute-Specific Performance

§101
37.0%
-3.0% vs TC avg
§103
41.9%
+1.9% vs TC avg
§102
8.8%
-31.2% vs TC avg
§112
8.8%
-31.2% vs TC avg
Black line = Tech Center average estimate • Based on career data from 331 resolved cases

Office Action

§101 §103
DETAILED ACTION Claims 1, 3, 6, 8, 14, 17-19, 21, 24-26, 31, 34, 38-39, 49, & 53-58 are currently pending and have been examined. This action is in response to the amendment filed on 6/3/2026 Notice of Pre-AIA or AIA Status The present application, filed on or after March 16, 2013, is being examined under the first inventor to file provisions of the AIA . Claim Rejections - 35 USC § 101 35 U.S.C. 101 reads as follows: Whoever invents or discovers any new and useful process, machine, manufacture, or composition of matter, or any new and useful improvement thereof, may obtain a patent therefor, subject to the conditions and requirements of this title. Claims 1, 3, 6, 8, 14, 17-19, 21, 24-26, 31, 34, 38-39, 49, & 53-58 are rejected under 35 U.S.C. §101 because the claimed invention is directed to an abstract idea without significantly more. Subject Matter Eligibility Criteria - Step 1: Claim 49 is directed to a system (i.e., a machine); Claims 1, 3, 6, 8, 14, 17-19, 21, 24-26, 31, 34, 38-39, & 53-58 are directed to a method (i.e., a process). Accordingly, claims 1, 3, 6, 8, 14, 17-19, 21, 24-26, 31, 34, 38-39, 49, & 53-58 are all within at least one of the four statutory categories. Subject Matter Eligibility Criteria - Alice/Mayo Test: Step 2A - Prong One: Regarding Prong One of Step 2A, the claim limitations are to be analyzed to determine whether, under their broadest reasonable interpretation, they “recite” a judicial exception or in other words whether a judicial exception is “set forth” or “described” in the claims. MPEP 2106.04(II)(A)(1). An “abstract idea” judicial exception is subject matter that falls within at least one of the following groupings: a) certain methods of organizing human activity, b) mental processes, and/or c) mathematical concepts. MPEP 2106.04(a). Independent claim 26 includes limitations that recite at least one abstract idea. Specifically, independent claim 26 recites: 26. A method comprising: receiving sensor data from one or more sensors, at least a portion of the sensor data being generated and received during a sleep session of a user while the user is asleep; determining one or more physiological parameters based on the received sensor data; generating a sleep disorder prediction that the user is experiencing a first sleep disorder based at least in part on the one or more physiological parameters; identifying a future sleep therapy plan for user associated with a second sleep disorder that is different than the first sleep disorder; generating a recommended modification to the future sleep therapy plan based at least in part on the generated sleep disorder prediction and the future sleep therapy plan; and automatically applying recommended modification to the future sleep therapy plan prior to implementation of the future sleep therapy plan during a future sleep session by adjusting one or more sleep therapy parameters of the future sleep therapy plan. The Examiner submits that the foregoing underlined limitations constitute “methods of organizing human activity” because receiving sensor data, receiving sleep therapy parameters, determining a sleep disorder based on user parameter data, generating updating therapy parameters based on the sensor and parameter data, and presenting the updated parameters are associated with managing personal behavior or relationships or interactions between people. For example, but for the system, this claim encompasses a person facilitating data access, receiving data, and outputting data in the manner described in the identified abstract idea. The Examiner notes that “method of organizing human activity” includes a person’s interaction with a computer – see MPEP 2106.04(a)(2)(II)(C). If a claim limitation, under its broadest reasonable interpretation, covers managing personal behavior or interactions between people but for the recitation of generic computer components, then it falls within the “method of organizing human activity” grouping of abstract ideas. Accordingly, the claim recites an abstract idea. Representative independent claim 49 includes limitations that recite at least one abstract idea. Specifically, independent claim 49 recites: 49. A system comprising: a control system including one or more processors; and a memory having stored thereon machine readable instructions; wherein the control system is coupled to the memory, and wherein the one or more processors of the control system are configured to execute the machine readable instructions in the memory to: receive sensor data from one or more sensors, the sensor data being associated with a user engaging in a sleep therapy plan; the sensor data being generated and received during a sleep session of the user while the user is asleep, the sleep therapy plan including a target value of a sleep quality metric; determine a current value of the sleep quality metric based on the sensor data; identify a difference between the target value of the sleep quality metric and the current value of the sleep quality metric; receive one or more therapy parameters associated with the sleep therapy plan; dynamically generate at least one updated therapy parameter associated with the sleep therapy plan based at least in part on the difference between the target value of the sleep quality metric and the current value of the sleep quality metric; and automatically apply the at least one updated therapy parameter to the sleep therapy plan to modify the sleep session and achieve the target value of the sleep quality metric for the sleep session, or to modify a future sleep session and achieve the target value of the sleep quality metric for the future sleep session The Examiner submits that the foregoing underlined limitations constitute “methods of organizing human activity” because receiving sensor data, receiving sleep therapy parameters, generating updating therapy parameters based on the sensor and parameter data, and presenting the updated parameters are associated with managing personal behavior or relationships or interactions between people. For example, but for the system, this claim encompasses a person facilitating data access, receiving data, and outputting data in the manner described in the identified abstract idea. The Examiner notes that “method of organizing human activity” includes a person’s interaction with a computer – see MPEP 2106.04(a)(2)(II)(C). If a claim limitation, under its broadest reasonable interpretation, covers managing personal behavior or interactions between people but for the recitation of generic computer components, then it falls within the “method of organizing human activity” grouping of abstract ideas. Accordingly, the claim recites an abstract idea. Accordingly, independent claims 26 & 49 and analogous independent claim 1 recite at least one abstract idea. Furthermore, dependent claims 3, 6, 8, 14, 17-19, 21, 24-25, 31, 34, 38-39, & 53-58 further narrow the abstract idea described in the independent claims. Claims 3, 6, 8, 14, 17, 24-25, 39, 54-56 & 58 recite presenting updated therapy parameters and generating a new therapy plan, Claims 21, 31, 34 recite determining sleep quality information and generating a sleep quality score, Claim 53 recites a sleep quality metric. These limitations only serve to further limit the abstract idea and hence, are directed towards fundamentally the same abstract idea as independent claims 26 & 49 and analogous independent claim 1, even when considered individually and as an ordered combination. Subject Matter Eligibility Criteria - Alice/Mayo Test: Step 2A - Prong Two: Regarding Prong Two of Step 2A of the Alice/Mayo test, it must be determined whether the claim as a whole integrates the abstract idea into a practical application. As noted at MPEP §2106.04(II)(A)(2), it must be determined whether any additional elements in the claim beyond the abstract idea integrate the exception into a practical application in a manner that imposes a meaningful limit on the judicial exception. The courts have indicated that additional elements merely using a computer to implement an abstract idea, adding insignificant extra solution activity, or generally linking use of a judicial exception to a particular technological environment or field of use do not integrate a judicial exception into a “practical application.” MPEP §2106.05(I)(A). In the present case, the additional limitations beyond the above-noted at least one abstract idea recited in the claim are as follows (where the bolded portions are the “additional limitations” while the underlined portions continue to represent the at least one “abstract idea”): 26. A method comprising: receiving sensor data from one or more sensors, at least a portion of the sensor data being generated and received during a sleep session of a user while the user is asleep; determining one or more physiological parameters based on the received sensor data; generating a sleep disorder prediction that the user is experiencing a first sleep disorder based at least in part on the one or more physiological parameters; identifying a future sleep therapy plan for user associated with a second sleep disorder that is different than the first sleep disorder; generating a recommended modification to the future sleep therapy plan based at least in part on the generated sleep disorder prediction and the future sleep therapy plan; and automatically applying recommended modification to the future sleep therapy plan prior to implementation of the future sleep therapy plan during a future sleep session by adjusting one or more sleep therapy parameters of the future sleep therapy plan. 49. A system comprising: a control system including one or more processors; and a memory having stored thereon machine readable instructions; wherein the control system is coupled to the memory, and wherein the one or more processors of the control system are configured to execute the machine readable instructions in the memory to: receive sensor data from one or more sensors, the sensor data being associated with a user engaging in a sleep therapy plan; the sensor data being generated and received during a sleep session of the user while the user is asleep, the sleep therapy plan including a target value of a sleep quality metric; determine a current value of the sleep quality metric based on the sensor data; identify a difference between the target value of the sleep quality metric and the current value of the sleep quality metric; receive one or more therapy parameters associated with the sleep therapy plan; dynamically generate at least one updated therapy parameter associated with the sleep therapy plan based at least in part on the difference between the target value of the sleep quality metric and the current value of the sleep quality metric; and automatically apply the at least one updated therapy parameter to the sleep therapy plan to modify the sleep session and achieve the target value of the sleep quality metric for the sleep session, or to modify a future sleep session and achieve the target value of the sleep quality metric for the future sleep session For the following reasons, the Examiner submits that the above identified additional limitations do not integrate the above-noted at least one abstract idea into a practical application. Regarding the additional limitations of the control system, processor, memory; the Examiner submits that these limitations amount to merely using computers as tools to perform the above-noted at least one abstract idea (see MPEP § 2106.05(f)). Regarding the additional limitation of a sensor, the Examiner submits that these additional limitations do no more than generally link use of the abstract idea to a particular technological environment or field of use without altering or affecting how the steps of the at least one abstract idea are performed (see MPEP § 2106.05(h)). Thus, taken alone, the additional elements do not integrate the at least one abstract idea into a practical application. Looking at the additional limitations as an ordered combination adds nothing that is not already present when looking at the elements taken individually. For instance, there is no indication that the additional elements, when considered as a whole with the abstract idea, reflect an improvement in the functioning of a computer or an improvement to another technology or technical field, apply or use the above-noted judicial exception to effect a particular treatment or prophylaxis for a disease or medical condition, implement/use the above-noted judicial exception with a particular machine or manufacture that is integral to the claim, effect a transformation or reduction of a particular article to a different state or thing, or apply or use the judicial exception in some other meaningful way beyond generally linking the use of the judicial exception to a particular technological environment, such that the claim as a whole does not integrate the abstract idea into a practical application of the abstract idea. MPEP §2106.05(I)(A) and §2106.04(II)(A)(2). For these reasons, independent claims 26 & 49 and analogous independent claim 1 do not recite additional elements that integrate the judicial exception into a practical application. Accordingly, the claims recite at least one abstract idea. The remaining dependent claim limitations not addressed above fail to integrate the abstract idea into a practical application as set forth below: Claims 17-19, 38: These claims recite various sensors and thus do no more than generally link use of the abstract idea to a particular technological environment or field of use without altering or affecting how the at least one abstract idea is performed (see MPEP § 2106.05(h)). Claims 55-58: These claims recite applying parameters such environmental and other parameters to effect a physical impact to the user and amounts to no more than a recitation of the words “apply it” because they are an attempt to cover any solution to an identified problem with no restriction on how the result is accomplished and no description of the mechanism for accomplishing the result– see MPE 2106.05(f). Thus, taken alone, any additional elements do not integrate the at least one abstract idea into a practical application. Therefore, the claims are directed to at least one abstract idea. Subject Matter Eligibility Criteria - Alice/Mayo Test: Step 2B: Regarding Step 2B of the Alice/Mayo test, representative independent claim 49 does not include additional elements (considered both individually and as an ordered combination) that are sufficient to amount to significantly more than the judicial exception for reasons the same as those discussed above with respect to determining that the claim does not integrate the abstract idea into a practical application. As discussed above, regarding the additional limitations of the control system, processor, memory; the Examiner submits that these limitations amount to merely using computers as tools to perform the above-noted at least one abstract idea (see MPEP § 2106.05(f)). Regarding the additional limitation of a sensor, the Examiner submits that these additional limitations do no more than generally link use of the abstract idea to a particular technological environment or field of use without altering or affecting how the steps of the at least one abstract idea are performed (see MPEP § 2106.05(h)). The dependent claims also do not include additional elements (considered both individually and as an ordered combination) that are sufficient to amount to significantly more than the judicial exception for the same reasons to those discussed above with respect to determining that the dependent claims do not integrate the at least one abstract idea into a practical application. Therefore, claims 1, 3, 6, 8, 14, 17-19, 21, 24-26, 31, 34, 38-39, 49, & 53-58 are ineligible under 35 USC §101. Claim Rejections - 35 USC § 103 The following is a quotation of 35 U.S.C. 103 which forms the basis for all obviousness rejections set forth in this Office action: A patent for a claimed invention may not be obtained, notwithstanding that the claimed invention is not identically disclosed as set forth in section 102, if the differences between the claimed invention and the prior art are such that the claimed invention as a whole would have been obvious before the effective filing date of the claimed invention to a person having ordinary skill in the art to which the claimed invention pertains. Patentability shall not be negated by the manner in which the invention was made. The factual inquiries for establishing a background for determining obviousness under 35 U.S.C. 103 are summarized as follows: 1. Determining the scope and contents of the prior art. 2. Ascertaining the differences between the prior art and the claims at issue. 3. Resolving the level of ordinary skill in the pertinent art. 4. Considering objective evidence present in the application indicating obviousness or nonobviousness. Claims 1, 3, 6, 8, 14, 17-18, 25, 49, 53, 55-58 are rejected under 35 U.S.C. 103 as being unpatentable over Moturu (US20170189641). As per claim 1, Moturu discloses a method, comprising: receiving sensor data from one or more sensors, the sensor data being associated with a user engaging in a sleep therapy plan, the sensor data being generated and received during a sleep session of the user while the user is asleep, the sleep therapy plan including a target value of a sleep quality metric (para. 46, 66: sensor data obtained from user regarding sleep quality generated and received during user sleep session; data includes determining a sleep quality parameter; sleep care plan determined including thresholds for sleep-related parameters); determining a current value of the sleep quality metric based on the sensor data (para. 46, 66: sensor data obtained from user regarding sleep quality generated and received during user sleep session; data includes determining a sleep quality parameter); identifying a difference between the target value of the sleep quality metric and the current value of the sleep quality metric (para. 66: mapping a sleep-related parameter value (e.g., falling within a range; satisfying a threshold condition; of a certain type and magnitude; etc.) to one or more therapeutic intervention types associated with the sleep quality parameter value); receiving one or more therapy parameters associated with the sleep therapy plan (para. 55, 67-68: therapeutic intervention model generates parameters based on sleep care plan); dynamically generating at least one updated therapy parameter associated with the sleep therapy plan based at least in part on the difference between the target value of the sleep quality metric and the current value of the sleep quality metric (para. 65-69: sleep care plan is updated based on evaluation of improvement of user’s sleep quality using sleep-related parameters; plan parameters can be changed to improve user’s sleep quality; for example generating a therapeutic intervention model based the correlation; and in response to characterizing a sleep latency above the threshold for a current user, determining a sleep care plan including a scheduled presentation of the sleep-related recommendation); and automatically applying the at least one updated therapy parameter to the sleep therapy plan to modify the sleep session and achieve the target value of the sleep quality metric for the sleep session, or to modify a future sleep session and achieve the target value of the sleep quality metric for the future sleep session (para. 61, 6: modification to sleep plan displayed; determining a therapeutic intervention (e.g., promoting a sleep-related notification in response to detecting activation of a native phone calling application in the bedroom during nighttime, based on device event data and motion supplementary data). As per claim 3, Moturu discloses the method of claim 1, wherein; the one or more therapy parameters associated with the sleep therapy plan include i) a target in-bed time; ii) a target out-of-bed time; iii) a target sleep time; iv) a target awaken time; v) an alarm time; vi) a target sleep duration; vii) a pharmacological dosage parameter; viii) a sleep environment parameter; ix) a pre-sleep activity parameter; or x) any combination of i-ix (para. 66: various therapy parameters); and wherein the at least one updated therapy parameter includes i) an updated in-bed time; ii) an updated out-of-bed time; iii) an updated target sleep time; iv) an updated target awaken time; v) an updated alarm time; vi) an updated target sleep duration; vii) updated pharmacological dosage parameter; viii) an updated sleep environment parameter; ix) an updated pre-sleep parameter; or x) any combination of i-ix (para. 66, 69: various sleep parameters can be updated). As per claim 6, Moturu discloses the method of claim 5, wherein the one or more therapy parameters includes an alarm time, wherein the at least one updated therapy parameter includes an updated alarm time, and wherein presenting the at least one updated therapy parameter includes adjusting the alarm time based at least in part on the updated alarm time (para. 62-63: provide the user with a personalized sleep care plan according to the user's desired sleep goals (e.g., wakeup times, bedtimes, etc.). As per claim 8, Moturu discloses the method of claim 1, wherein dynamically generating the at least one updated therapy parameter is further based at least in part on i) one or more sleep events detected based at least in part on the sensor data, ii) an apnea-hypopnea index calculated based at least in part on the sensor data, iii) sleep stage information based at least in part on the sensor data, or iv) any combination of i)-iii) (para. 44: generate values of sleep-related parameters associated with the time period (e.g., sleep session); such as sleep stage and sleep events). As per claim 14, Moturu discloses the method of claim 1, wherein dynamically generating the at least one updated therapy parameters includes: accessing a historical log associated with the sleep therapy plan (para. 69: first log of use dataset associated with therapeutic intervention); and generating the at least one updated therapy parameter based at least in part on the historical log (para. 69: dynamically updating care plan based on previous sleep session data associated with therapeutic intervention). As per claim 17, Moturu discloses the method of claim 1, wherein receiving the sensor data from the one or more sensors includes receiving non-contact sensor data from at least one non-contact sensor (para. 21, 33: non contact sensor such as GPS sensor), and wherein dynamically generating the at least one updated therapy parameter includes: extracting biomotion information based at least in part on the non-contact sensor data (para. 21: mobility behavior data extracted); identifying body movement information based at least in part on the extracted biomotion information (para. 53: extracting a set of features from a log of use dataset and a motion supplementary dataset); and generating the at least one updated therapy parameter based at least in part on the body movement information (para. 55, 60: sleep-related parameters extracted and used to generate updated sleep interventions). As per claim 18, Moturu discloses the method of claim 1, wherein receiving the sensor data from the one or more sensors includes receiving environment data from i) a temperature sensor; ii) a light sensor; iii) a presence sensor; iv) a microphone; or v) any combination of i-iv (para. 78: ambient data obtained from various sensors); and wherein dynamically generating the at least one updated therapy parameter is based at least in part on the environment data (para. 78: ambient data can be used to generate therapeutic intervention). As per claim 25, Moturu discloses the method of claim 1, wherein receiving the sensor data includes receiving additional sensor data while the user is not engaging in the sleep session (para. 46: sensor data obtained in other activities), and wherein dynamically generating the at least one updated therapy parameter is based at least in part on the sensor data generated during the sleep session and additional sensor data generated while the user is not engaging in the sleep session (para. 46, 60-65: sleep data uses sensor data from various sensors obtaining data at various times including sleep and waking sessions; sleep therapeutic intervention determined based on obtained sleep data). As per claim 49, Moturu discloses a system comprising: a control system including one or more processors (para. 79: processor); and a memory having stored thereon machine readable instructions; wherein the control system is coupled to the memory, and wherein the one or more processors of the control system are configured to execute the machine readable instructions in the memory to: receive sensor data from one or more sensors, the sensor data being associated with a user engaging in a sleep therapy plan, the sensor data being generated and received during a sleep session of the user while the user is asleep, the sleep therapy plan including a target value of a sleep quality metric (para. 46, 66: sensor data obtained from user regarding sleep quality generated and received during user sleep session; data includes determining a sleep quality parameter; sleep care plan determined including thresholds for sleep-related parameters); determining a current value of the sleep quality metric based on the sensor data (para. 46, 66: sensor data obtained from user regarding sleep quality generated and received during user sleep session; data includes determining a sleep quality parameter); identifying a difference between the target value of the sleep quality metric and the current value of the sleep quality metric (para. 66: mapping a sleep-related parameter value (e.g., falling within a range; satisfying a threshold condition; of a certain type and magnitude; etc.) to one or more therapeutic intervention types associated with the sleep quality parameter value); receiving one or more therapy parameters associated with the sleep therapy plan (para. 55, 67-68: therapeutic intervention model generates parameters based on sleep care plan); dynamically generating at least one updated therapy parameter associated with the sleep therapy plan based at least in part on the difference between the target value of the sleep quality metric and the current value of the sleep quality metric (para. 65-66, 69: sleep care plan is updated based on evaluation of improvement of user’s sleep quality using sleep-related parameters; plan parameters can be changed to improve user’s sleep quality); and automatically applying the at least one updated therapy parameter to the sleep therapy plan to modify the sleep session and achieve the target value of the sleep quality metric for the sleep session, or to modify a future sleep session and achieve the target value of the sleep quality metric for the future sleep session (para. 61, 6: modification to sleep plan displayed; determining a therapeutic intervention (e.g., promoting a sleep-related notification in response to detecting activation of a native phone calling application in the bedroom during nighttime, based on device event data and motion supplementary data). As per claim 53, Moturu discloses the method of claim 1, wherein the sleep quality metric includes a sleep duration, a sleep efficiency, or both (para. 44: sleep parameters determined including sleep efficiency). As per claim 55, Moturu discloses the method of claim 1, wherein the updated therapy parameter includes an environmental parameter, and wherein applying the updated environmental parameter includes adjusting a physical environment of the user during the sleep session or the future sleep session (para. 70: promoting a therapeutic intervention to the user according to the sleep care plan including adjusting temperature or lighting systems). As per claim 56, Moturu discloses the method of claim 55, wherein the environmental parameter includes a light level in the physical environment of the user, a temperature level in the physical environment of the user, a sound level in the physical environment of the user, a humidity level in the physical environment of the user, or any combination thereof (para. 70: promoting a therapeutic intervention to the user according to the sleep care plan including adjusting temperature or lighting systems). As per claim 57, Moturu discloses the method of claim 1, wherein automatically applying the updated therapy parameter includes effecting a physical impact to the user that modifies the sleep session or the future sleep session (para. 70: promoting a therapeutic intervention to the user according to the sleep care plan including adjusting temperature or lighting systems). As per claim 58, Moturu discloses the method of claim 57, wherein the physical impact to the user includes an update to an alarm time of a device of the user, a change in a light level in a physical environment of the user, a change in a temperature level in the physical environment of the user, a change in a sound level in the physical environment of the user, a change in a humidity level in the physical environment of the user, or any combination thereof (para. 70: promoting a therapeutic intervention to the user according to the sleep care plan including adjusting temperature or lighting systems) Claim Rejections - 35 USC § 103 The following is a quotation of 35 U.S.C. 103 which forms the basis for all obviousness rejections set forth in this Office action: A patent for a claimed invention may not be obtained, notwithstanding that the claimed invention is not identically disclosed as set forth in section 102, if the differences between the claimed invention and the prior art are such that the claimed invention as a whole would have been obvious before the effective filing date of the claimed invention to a person having ordinary skill in the art to which the claimed invention pertains. Patentability shall not be negated by the manner in which the invention was made. The factual inquiries for establishing a background for determining obviousness under 35 U.S.C. 103 are summarized as follows: 1. Determining the scope and contents of the prior art. 2. Ascertaining the differences between the prior art and the claims at issue. 3. Resolving the level of ordinary skill in the pertinent art. 4. Considering objective evidence present in the application indicating obviousness or nonobviousness. Claim 19 is rejected under 35 U.S.C. 103 as being unpatentable over Moturu in view of Ning (US20180060507). As per claim 19, Moturu teaches the method of claim 1, but does not expressly teach wherein receiving the sensor data from the one or more sensors includes receiving pharmacological data from i) a pharmacological container sensor; ii) a camera; iii) a weight sensor; or iv) any combination of i-iii; and wherein dynamically generating the at least one updated therapy parameter is based at least in part on the pharmacological data. Ning, however, teaches to a method for optimized wake-up strategy via sleeping stage prediction with recurrent neural networks where a sensor such as a camera is used to obtain user sleep data (para. 27). Ning also teaches to using the sensor data to generate new patient sleep intervention plan (para. 39). It would have been obvious for one of ordinary skill in the art before the effective filing date of the claimed invention to combine the aforementioned features in Ning with Moturu based on the motivation of provides a system for optimized wake-up strategy via sleeping stage prediction with recurrent neural networks (Ning – para. 22). Claims 21, 24, & 54 are rejected under 35 U.S.C. 103 as being unpatentable over Moturu in view of Molina (US20190083028). As per claim 21, Moturu teaches the method of claim 1, further comprising: determining sleep quality information based at least in part on the sensor data, the sleep quality information including i) sleep efficacy information; ii) sleep state information; iii) sleep stage information; iv) detected sleep event information; v) a calculated apnea-hypopnea index; vi) or any combination of i)-v) (para. 144: sleep quality parameters extracted). Moturu does not expressly teach generating a sleep therapy plan score based at least in part on the sleep quality information; and storing the sleep therapy plan score in association with the one or more therapy parameters of the sleep therapy plan. Molina, however, teaches to facilitating sleep improvement for a user where a score is generated and stored based on sleep parameter data together in a database (para. 84, 85). It would have been obvious for one of ordinary skill in the art before the effective filing date of the claimed invention to combine the aforementioned features in Molina with Moturu based on the motivation of provide a meaningful and quantifiable metric for an individual to understand a quality of his/her sleep (Molina – para. 3). As per claim 24, Moturu and Molina teach the method of claim 21. Moturu does not expressly teach wherein dynamically generating the at least one updated therapy parameter includes: accessing a historical sleep therapy plan score associated with one or more historical parameters; comparing the historical sleep therapy plan score with the sleep therapy plan score; and generating the at least one updated therapy parameter based at least in part on the one or more historical parameters, the one or more parameters, and the comparison between the historical sleep therapy plan score and the sleep therapy plan score. Molina, however, teaches to facilitating sleep improvement for a user where a score is generated and stored based on sleep parameter data together in a database (para. 84, 85). Molina also teaches to accessing historical sleep scores and metrics and comparing those metrics with reference metrics (para. 37). Molina also teaches to generating new sleep parameters based on the comparison (para. 83, 89, 91). The motivations to combine the above mentioned references are discussed in the rejection of claim 21, and incorporated herein As per claim 54, Moturu teaches the method of claim 1, but does not expressly teach wherein the updated therapy parameter includes an updated alarm time, and wherein applying the updated alarm time includes adjusting an alarm time of a device of the user to match the updated alarm time. Molina, however, teaches to facilitating sleep improvement for a user where a sleep intervention can be determined including audible tones may be output by an auditory stimulation device (e.g., an audible alarm clock, music player, etc.) (para. 41). The motivations to combine the above mentioned references are discussed in the rejection of claim 21, and incorporated herein Claims 26, 31, 34, & 38-39 are rejected under 35 U.S.C. 103 as being unpatentable over Moturu in view of Munafo (US20160210440). As per claim 26, Moturu discloses a method comprising: receiving sensor data from one or more sensors, at least a portion of the sensor data being generated and received during a sleep session of a user while the user is asleep (para. 46: sensor data obtained from user regarding sleep quality); determining one or more physiological parameters based on the received sensor data (para. 44: sleep-related parameters determined); generating a sleep disorder prediction that the user is experiencing a first sleep disorder based at least in part on the one or more physiological parameters (para. 44, 60: diagnosis can be characterized based on analysis of sleep parameters); automatically applying recommended modification to the future sleep therapy plan prior to implementation of the future sleep therapy plan during a future sleep session by adjusting one or more sleep therapy parameters of the future sleep therapy plan. (para. 65-66, 69: sleep care plan is updated based on evaluation of improvement of user’s sleep quality using sleep-related parameters; plan parameters can be changed to improve user’s sleep quality). Moturu does not expressly teach identifying a future sleep therapy plan for user associated with a second sleep disorder that is different than the first sleep disorder; generating a recommended modification to the future sleep therapy plan based at least in part on the generated sleep disorder prediction and the future sleep therapy plan. Munafo, however, teaches to identifying multiple sleeping disorders from a patient using input data and identifying a therapeutic regimen that addresses both disorders (para. 23). It would have been obvious for one of ordinary skill in the art before the effective filing date of the claimed invention to combine the aforementioned features in Munafo with Moturu based on the motivation of achieving satisfactory compliance for a therapy to address a disorder (Munafo – para. 3). As per claim 31, Moturu and Munafo teach the method of claim 26. Moturu teaches wherein the sensor data includes subjective user feedback associated with a sleep session (para. 38: survey dataset from user), wherein the method further comprises generating a sleep score indicative of a stress level of the user based at least in part on the subjective user feedback (para. 40-41: survey dataset includes stress level data and generating a quantitative score), and wherein identifying the future sleep therapy plan is based at least in part on the stress score (para. 66: sleep care plan can be generated using survey dataset). As per claim 34, Moturu and Munafo teach the method of claim 26. Moturu teaches further comprising generating a sleep quality log based at least in part on the sensor data, wherein the sleep quality log includes i) sleep state information; ii) sleep stage information; iii) subjective user feedback associated with a sleep session, or iv) any combination of i)-iii) (para. 66: determining sleep care plan based on sleep-related parameter mapped to specific therapeutic intervention types associated with the sleep quality parameter value); wherein identifying the future sleep therapy plan is based at least in part on the sleep quality log (para. 55, 60: sleep-related parameters extracted and used to generate updated sleep interventions). Claim 38 recites substantially similar limitations as those already addressed in claim 17, and, as such, is rejected for similar reasons as given above. As per claim 39, Moturu and Munafo teach the method of claim 26. Moturu teaches identifying the future sleep therapy plan includes: determining one or more sleep duration parameters associated with a target sleep duration used in the future sleep therapy plan, and wherein the sleep therapy plan recommendation includes i) suggested changes to at least one of the one or more sleep duration parameters, ii) suggested values for at least one of the one or more sleep duration parameters, or iii) both i and ii; automatically providing one or more default therapy parameters; determining one or more therapy parameters associated with the futures sleep therapy plan, wherein the one or more sleep therapy parameters includes: i) a sleep restriction parameter; ii) a sleep compression parameter; iii) a pharmacological parameter; iv) a sleep onset latency parameter; v) a sleep environment parameter; vi) a pre-sleep activity parameter; or vii) any combination of i-vi; or determining that the future sleep therapy plan is a cognitive behavior therapy for insomnia (CBTi) plan. Response to Arguments Applicant’s arguments with respect to the 35 U.S.C. § 101 rejection on pages 10-14 in regards to claims 1, 3, 6, 8, 14, 17-19, 21, 24-26, 31, 34, 38-39, 49, & 53-58 have been considered but are not persuasive. Applicant argues that: The claims reflect an improvement to technology providing for closed-loop feedback control of therapy parameters during sleep. The Examiner, however, asserts that the instant application presents a non-technical problem – generating and recommending sleep therapy plans based on sleep data. The solution to the problem is rooted in an improvement to the abstract idea itself and not a technical failure of a computer system or technology. The additional elements can best be characterized as tools to perform an existing process and only amounts to an instruction to implement the abstract idea using a computer (MPEP § 2106.05(f)(2) see case requiring the use of software to tailor information and provide it to the user on a generic computer within the "Other examples., v."). The requirement of automatic action to change a physical process imposes a meaningful limit on the claims. The Examiner, however, asserts that the recitation of automatically applying parameters such environmental and other parameters to effect a physical impact to the user amounts to no more than a recitation of the words “apply it” because they are an attempt to cover any solution to an identified problem with no restriction on how the result is accomplished and no description of the mechanism for accomplishing the result– see MPE 2106.05(f). The claimed sensors are not a field-of-use limitation and are integral to the claimed feedback control loop. The Examiner, however, asserts that the sensors themselves are claimed at a high level of generality and this limitation merely confines the use of the abstract idea with using data collected by generically described sensors. Claim 26 describes a specific technological process for detecting comorbid sleep disorder conditions and cannot be practically performed by a human being managing personal behavior and is also a technological solution by using sensor-derived physiological data. The Examiner, however, asserts that as described above Claim 26 is directed to an abstract idea of solving a non-technical problem of detecting sleep disorder conditions and generating sleep therapy plans based on the detected conditions. The solution to the problem is rooted in an improvement to the abstract idea itself and not a technical failure of a computer system or technology. The additional elements can best be characterized as tools to perform an existing process and only amounts to an instruction to implement the abstract idea using a computer (MPEP § 2106.05(f)(2) see case requiring the use of software to tailor information and provide it to the user on a generic computer within the "Other examples., v."). Claim 26 also requires the system to take concrete, autonomous action that modifies the future sleep plan. The Examiner, however, asserts that the recitation of automatically applying parameters such environmental and other parameters to effect a physical impact to the user amounts to no more than a recitation of the words “apply it” because they are an attempt to cover any solution to an identified problem with no restriction on how the result is accomplished and no description of the mechanism for accomplishing the result– see MPE 2106.05(f). Example 46 Claim 3 included limitations such as where a sorting gate was controlled by a processor via the sending of a control signal. The same cannot be said here. There is no control signal claimed by Applicant that causes a real-world control of a physical structure or device. Applicant’s arguments with respect to the 35 U.S.C. § 103(a) rejection on pages 14-15 in regards to claims 1, 3, 6, 8, 14, 17-19, 21, 24-26, 31, 34, 38-39, 49, & 53-58 have been considered but are moot in view of the new ground(s) of rejection. Conclusion The prior art made of record and not relied upon is considered pertinent to applicant's disclosure. Heneghan (US20220061752) teaches to a system for monitoring a user's fatigue state, the system comprising one or more data sources such as objective measures of sleep and SDB, subjective user data, objective fatigue measurements, and environmental data, and a monitoring module that analyses the data to generate an assessment of the fatigue state of the user. Shouldice (US20160151603) teaches to a method of a processor for promoting sleep of a user. The method may involve with a processor, analyzing signals from a motion sensor to detect sleep information from the signals. The method may involve with the processor, upon receiving an activation signal, recording by a microphone a voice sound message of the user and storing data of the voice sound message in a memory coupled to the processor. The method may permit a user to record thoughts so as to clear a mind of the user and promote sleep. Applicant's amendment necessitated the new ground(s) of rejection presented in this Office action. Accordingly, THIS ACTION IS MADE FINAL. See MPEP § 706.07(a). Applicant is reminded of the extension of time policy as set forth in 37 CFR 1.136(a). A shortened statutory period for reply to this final action is set to expire THREE MONTHS from the mailing date of this action. In the event a first reply is filed within TWO MONTHS of the mailing date of this final action and the advisory action is not mailed until after the end of the THREE-MONTH shortened statutory period, then the shortened statutory period will expire on the date the advisory action is mailed, and any nonprovisional extension fee (37 CFR 1.17(a)) pursuant to 37 CFR 1.136(a) will be calculated from the mailing date of the advisory action. In no event, however, will the statutory period for reply expire later than SIX MONTHS from the mailing date of this final action. Any inquiry concerning this communication or earlier communications from the examiner should be directed to Jonathan K Ng whose telephone number is (571)270-7941. The examiner can normally be reached M-F 8 AM - 5 PM. Examiner interviews are available via telephone, in-person, and video conferencing using a USPTO supplied web-based collaboration tool. To schedule an interview, applicant is encouraged to use the USPTO Automated Interview Request (AIR) at http://www.uspto.gov/interviewpractice. If attempts to reach the examiner by telephone are unsuccessful, the examiner’s supervisor, Anita Coupe can be reached at 571-270-7949. The fax phone number for the organization where this application or proceeding is assigned is 571-273-8300. Information regarding the status of published or unpublished applications may be obtained from Patent Center. Unpublished application information in Patent Center is available to registered users. To file and manage patent submissions in Patent Center, visit: https://patentcenter.uspto.gov. Visit https://www.uspto.gov/patents/apply/patent-center for more information about Patent Center and https://www.uspto.gov/patents/docx for information about filing in DOCX format. For additional questions, contact the Electronic Business Center (EBC) at 866-217-9197 (toll-free). If you would like assistance from a USPTO Customer Service Representative, call 800-786-9199 (IN USA OR CANADA) or 571-272-1000. /Jonathan Ng/ Primary Examiner, Art Unit 3619
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Prosecution Timeline

Feb 28, 2024
Application Filed
Dec 12, 2025
Non-Final Rejection mailed — §101, §103
May 22, 2026
Interview Requested
Jun 02, 2026
Applicant Interview (Telephonic)
Jun 02, 2026
Examiner Interview Summary
Jun 03, 2026
Response Filed
Aug 25, 2026
Final Rejection mailed — §101, §103 (current)

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Study what changed to get past this examiner. Based on 5 most recent grants.

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Prosecution Projections

3-4
Expected OA Rounds
36%
Grant Probability
50%
With Interview (+14.0%)
3y 10m (~1y 3m remaining)
Median Time to Grant
Moderate
PTA Risk
Based on 331 resolved cases by this examiner. Grant probability derived from career allowance rate.

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