53 results about "Patient participation" patented technology

A medical information management system and method that stores and manages patient information and that enables a patient and an authorized third party, such as a friend or family member, to access the patient's medical information. The presentation format, substance of the patient's medical information provided, or both are customized depending on whether the patient, a healthcare professional or the third party is accessing the patient's medical information. The present invention also pertains to a method of subsidizing such a medical information system by selling advertising space in the presentation shown to the third party, patient, or the healthcare professional. The present invention further pertains to a patient interface appliance that includes a display containing multiple viewing fields, one of which is a general information field and one of which is an advertising field, to present information and advertisements to a user during a patient interactive session. Patient participation in conducting the survey is fostered by offering a survey completion reward to the patient upon completing the survey.

A method is proposed for monitoring participation of a patient in at least one clinical trial. The method includes collecting data regarding at least one clinical trial for the patient. Using a computer device, the collected data is then compared to at least one threshold. Finally, the patient is rewarded upon the collected data at least meeting at least one threshold.

A programmable rules-based interface between a patient and an electronic medical record EMR allows controlled patient access to the EMR allowing increased patient participation in the healthcare process. The interface allows the patient to directly schedule appointments for procedures, while filtering requests from patients who are not eligible for a given treatment, thereby limiting waste in resources.

A programmable rules-based interface between a patient and an electronic medical record EMR allows controlled patient access to the EMR allowing increased patient participation in the healthcare process.

A method and system are described for centrally managing data in an adaptive clinical trial or other adaptive process that is conducted at a plurality of geographically remote sites. The invention includes (1) flexible means for collecting data from remote sites; (2) processing, tracking, and validating such data and meta-data at a processing location; (3) interacting between central and remote sites to manage and resolve data discrepancies (4) reporting data to managers and remote sites; and (5) facilitation of special services to clinical research such as flexible randomization of patients, patient participation eligibility verification and double-blind trials. The invention is of particular relevance to adaptive clinical trials and other applications that demand the ability to quickly collect, process, and respond to various forms of data in order to adjust actions such as randomization schedules, interim analyses, treatment arm pruning, editing subpopulations, and other adaptive measures.

A system provides a clinical trial or research process with access to, and use of information employed in patient care by facilitating access to information via a portal (e.g., a Web compatible portal) and providing automated transfer of data collected during patient care workflows for storage in clinical research information systems. An interface system enables bidirectional exchange of data between a hospital clinical information system and a clinical trial or research information system. The interface system employs at least one repository including information associating a clinical trial with patient identifiers, healthcare worker identifiers, an indicator of individual status of a patient in the clinical trial and an identifier of a site involved in the clinical trial. An interface processor provides medical information of a particular patient, acquired using a hospital clinical information system, to a clinical trial or research storage repository by using information derived from the at least one repository for automatically determining, the particular patient is enrolled in a clinical trial and the particular patient participation in the clinical trial is still current.

Methods and systems for patient participatory care and monitoring are provided for applications including respiratory care, ECG monitoring, capnography, infusion pump alarm prevention / management, pressure sore prevention, incentive spirometry, consciousness monitoring during sedation, pain management and other care and monitoring modalities. A patient in-the-loop system includes an input interface for receiving data acquired from a monitoring, controlling or sensing device, a storage device for storing the data at a first location, and a processor for analyzing artifacts in the data and determining whether the patient provided a deliberate action with respect to the device as a response to a prompt or query. The processor can further initiate a variety of prompts and / or output queries stored in the storage device at a second location to the patient. The data derived from these patient-in-the-loop techniques are formatted to be received and interpreted by electronic medical record and electronic record keeping systems.

Method, Apparatus and non-transitory computer readable media that enhance patient-recruitment and participation in clinical trials preferably includes structure and / or steps whereby one or more APIs are used to interface at least one Cognitive Analytics Value Inference and Intelligence—Healthcare (CAVII-H) server with the patient(s), Pharma participant(s), Contract Research Organization(s), Trial Investigator(s), and Healthcare Providers (such as a physician). The at least one CAVII-H server preferably use at least one of stored trial data, user medical data, user behavioral date, user application collected data user registration data, healthcare professional data to guide patient participation. Preferably, information is obtained from the users through plural interactive algorithms designed to sharpen and perfect patient selection, preferably throughout the life of each trial. This creates a global clinical-trial patient engagement, recruitment and retention marketplace, which is open to patents and all trial stakeholders.

The method of the present invention is used to select high risk or co-morbid patients for participation in a care management program. An acuity score determines which patients are selected for care management.

The invention discloses an intelligent diagnosis and treatment management method and system and an intelligent clinic using the same. The system is an online and offline combined comprehensive servicesystem which takes clinics as a core and goes deep into a community; the system and the clinics are arranged throughout each population, and a patient can go to a nearby intelligent clinic at any time to complete registration, identity information binding and other things, so that subsequent direct diagnosis and treatment at any time are facilitated. The system and the clinics can perform preliminary registration and detection on basic health conditions, vital signs, genes and other information of a patient so as to provide medical / treatment suggestions for the patient, and the patient finally determines a treatment scheme; patients who cannot be treated by intelligent clinics can be treated; a plurality of selectable referral schemes are provided, referral appointment services without going out / community are provided for patients, and the patients can freely select the referral appointment services, so that the medical mode with hospitals as the core in a traditional medical system is broken through, and a brand-new medical mode with the patients as the core and with higher patient participation degree is established.

A web based electronic system with the capacity to record vital behavioral information while providing a platform for participating insurance companies to offer incentives for patients to engage in specific preventive care and / or health promotion practices. The system includes either an electronic funds transfer card that can be used as a debit or charge card to purchase goods and services, or a magnetic strip card as an ID to record the transaction. At checkout, the system operates invisibly to the consumer and the cashier. Approval of the transaction operates similarly to a conventional debit card or credit card. All incentives are managed by the data clearinghouse which receives patient data and provider data. The clearinghouse communicates with the insurance company and forwards a statement which displays the historical behavior.

Adequate patient enrollment and participation in different design stages of a clinical trial is facilitated and scaled by dynamically adjusting clinical trial criteria relative to characteristics and conditions of massive numbers of patients whose medical records have been aggregated in databases in compliance with patient privacy and confidentiality laws and regulations. Patient participation results without intervention by multiple providers of healthcare services, and by directly identifying and communicating with qualified patients while maintaining patient privacy and compliance requirements as required by law.

A clinical trial engagement tool and method execute on a mobile computing device. The tool includes displays of information containing pre-enrollment content based on searches executed on the mobile computing device, wherein access thereto is enabled without requirement of a user-specific login or security key. The tool includes displays containing clinical trial patient participation content, wherein access thereto is enabled only upon completion of a user authentication and authorization process. A tracking mechanism of the tool generates data that tracks which of the plurality of displays containing pre-enrollment content are accessed. The tool displays information containing notification content that is automatically selected for display based on the tracked data, thereby transforming the data into parameters that define which displays of notification content are automatically selected for display. The notification content includes information related to upcoming clinical trials having a potential to be of interest to the user of the device.

The invention discloses a hospital performance comprehensive management method based on the served number. The method comprises the following steps: S101, dividing the internal part of a hospital intoeight cooperative departments including a leader layer, a performance management office, a medical department, a nursing department, a channel management department, a hospital affair department, a medical insurance office and an outpatient office; and S102, classifying the assessment personnel of the hospital into class I assessment personnel and class II assessment personnel. The invention relates to the technical field of hospital performance management. The invention discloses a hospital performance comprehensive management method based on the served number. Detailed specific division iscarried out on departments, management personnel and medical personnel of a hospital; corresponding assessment methods and indexes are formulated, and the patients participate in the whole examinationwork, so that the whole examination work is fair and closely related to each examiner, the working enthusiasm of the actual medical personnel can be aroused, and the dilemma of 'secondary communal pot ' that clinical profit departments take commission, non-profit departments and administrative logistics departments take average awarding is overcome.

Adequate patient enrollment and participation in different design stages of a clinical trial is facilitated and scaled by dynamically adjusting clinical trial criteria relative to characteristics and conditions of massive numbers of patients whose medical records have been aggregated in databases in compliance with patient privacy and confidentiality laws and regulations. Patient participation results without intervention by multiple providers of healthcare services, and by directly identifying and communicating with qualified patients while maintaining patient privacy and compliance requirements as required by law.

An automated method and computer program product are provided for reporting payments made to patients for their participation in a clinical study in a blinded manner to the sponsor of the clinical study. The clinical study has a plurality of investigative sites which perform activities in accordance with the protocol of the clinical study. Each patient has patient ID information and is assigned a subject ID that de-identifies the patient. Payment requests are received at a software application from the investigative sites associated with patient activity. The software application includes for each patient that is participating in the clinical study, the patient ID information, and the de-identified subject ID. The payment requests are associated with the patient ID information. The payment requests are processed at the software application, and payments that conform to predefined compensation guidelines for the clinical study are approved. The software application generates blinded payment reports for electronic delivery to the sponsor. The payment reports show at least the de-identified subject ID for each approved payment, the payment amounts for each approved payment, and a date associated with the payment.

The invention discloses a patient administration system for a real world clinical study. The system is applied to patient administration in the real world clinical study. According to the system, systematic administration of patients is achieved through determination of patient participation in a project, patient screening, visiting administration, patient drop-out administration, patient privacy protection and the like, and the purposes of improving research quality and patient compliance are realized.

The invention discloses a method and a system for making an electronic prescription. The patient information is transmitted to a pharmaceutical company terminal through a patient terminal, the pharmaceutical company terminal provides a drug list to the patient terminal, the patient terminal acquires the drug list which is transmitted by the pharmaceutical company terminal and corresponding to thepatient information and then transmits the drug list and the patient information to a physician terminal, the physician terminal returns the physician's opinion on medication corresponding to the patient information and the drug list and made by the physician to the patient terminal, and finally the patient terminal generates the electronic prescription including the patient information, the druglist and the physician's opinion on medication so that the technical problems that the problems of the present electronic prescription making method that the demand of the patient for knowing the electronic prescription is not considered, the patient participation is low, and the physician makes the wrong prescription which affects the condition of the patient and event threatens the life of the patient are not improved can be solved.

The present invention lies in the field of simulation systems for medical treatments, in particular for treatments carried out on dialysis machines. To do so, a method with which medical treatments can be performed and evaluated without the involvement of real human patients is proposed.

The invention discloses a system for assisting and supporting a primary liver cancer patient to participate in treatment decision. According to the system, by using a mobile technology, different treatment scheme information data of primary liver cancer are presented to a patient through a data storage device; and according to different selectable treatment schemes corresponding to each patient, the patient is assisted to participate in treatment decision path selection, so that the patient can define own tendency selection in numerous selectable treatment schemes and make a treatment scheme selection most suitable for the patient together by combining opinions and suggestions of clinicians. According to the invention, detailed information data related to liver cancer treatment of a patient is provided, so that the patient can be helped to communicate with a doctor easily, doctor-patient accurate communication is promoted, the patient is helped to grow into an intelligent patient, thepatient is weighted, the treatment decision-making ability of the patient is improved, the health promotion capability of an authoritative liver cancer treatment institution is improved, reference isprovided for promoting the domestic doctor-patient sharing decision concept and other disease decision platform construction, and good social benefits and popularization value are achieved.

A programmable rules-based interface between a patient and an electronic medical record EMR allows controlled patient access to the EMR allowing increased patient participation in the healthcare process.

A plurality of instances of a patient's health condition are received as patient health information from a plurality of sources. Ground-truth health conditions of the patient are generated based on the patient health information and expert review of the patient's level of engagement for each instance of provider assessment. A regression model predicting a probability of patient engagement level with a provider is generated, based on the instances of patient condition assessment and the engagement level expert review associated with each instance. A current set of patient information and natural language processing results of a dialog between the patient and a provider performing a condition assessment of the patient, are received. The current patient information and the dialog are applied to the regression model, determining a probability of patient engagement level. An indicator of the patient engagement level is sent to the provider's computing device.

The invention relates to a remote medical system based on a face identification set-top-box. The remote medical system comprises a face identification and fingerprint recording unit, a networking communication unit, a telephone set, a user safety certificating service unit, a remote medical server, a doctor desktop terminal and a medical record server. The remote medical system is advantageous inthat the remote medical system based on the face identification set-top-box has a networking communication function through a medical system so that the system can perform medical resource distributing operation on the patient, thereby realizing uniform medical resource distribution and preventing incapability of performing in-time diagnosis when a disease occurs. Furthermore the remote medical system has remote medical treatment capability and replaces an operator of a shop or a clinic for finishing image acquisition. Furthermore in a whole remote medical treatment process, the patient requires accompanying of professional personnel, and a defect of simplifying a patient participation process is not simplified. Furthermore through integration of medical system and the set-top-box, and utilization of the integrated member in remote medical treatment, medical treatment speed by the people is effectively improved.

The invention belongs to the technical field of digital treatment, and particularly relates to a digital treatment method for improving patient participation interest and improving treatment effect through a reward strategy, and the method comprises the following specific steps: S1, setting a patient participation target and scheme, and storing the target and scheme in a database; s2, the patient is promoted to participate in the activity and awarded according to the set scheme; s3, based on the manifestation of the patient, properly increasing and decreasing awards for the patient; and S4, further observing and deciding to increase or decrease the treatment strength on the patient. The emotion change condition of the patient is observed and recorded in a mode of promoting the patient to participate in the activity, the activity participation amount and the participation frequency are properly increased or decreased according to the activity participation condition and the condition, the method can be suitable for different patients, the dosage of medicine is reduced, and side effects caused by the medicine are reduced. The traditional Chinese medicine composition participates in collective activities, can inhibit neurological diseases, promotes communication between patients and people, and releases pressure from participating in activities.

Embodiments of the present disclosure relate to systems, methods, and user interfaces for providing intelligent touch care. More particularly, embodiments of the present disclosure utilizes contributing data elements in a community early warning score (CEWS) to predict touchpoint discipline and to recommend frequency, modality, and upstream transitions of care and outside service referrals for a patient in a community care setting. In response to a touch point (e.g., a change in condition or medication, a scheduled or unscheduled appointment, or a patient question), the CEWS can be utilized along with data in an EHR of a patient, data from a patient device, or data from a patient portal to initiate a follow-up (e.g., personal health question or encounter). Notification tools and scheduling functionality are provided via a user interface of the patient device to improve clinical workforce capacity, increase the number of patient touches, and encourage heightened patient engagement.

An automated method and computer program product are provided for reporting payments made to patients for their participation in a clinical study in a blinded manner to the sponsor of the clinical study. The clinical study has a plurality of investigative sites which perform activities in accordance with the protocol of the clinical study. Each patient has patient ID information and is assigned a subject ID that de-identifies the patient. Payment requests are received at a software application from the investigative sites associated with patient activity. The software application includes for each patient that is participating in the clinical study, the patient ID information, and the de-identified subject ID. The payment requests are associated with the patient ID information. The payment requests are processed at the software application, and payments that conform to predefined compensation guidelines for the clinical study are approved. The software application generates blinded payment reports for electronic delivery to the sponsor. The payment reports show at least the de-identified subject ID for each approved payment, the payment amounts for each approved payment, and a date associated with the payment.

Instruments of determined level of self-efficacy may be chosen dynamically for customized patient engagement, e.g., based on a patient's latent adherence trait estimated from lifestyle and other clinical data. Customization points in care plans may be identified, e.g., by monitoring an accumulative change in the patient's health literacy level. Clinical decision support at the point of care may be provided by adjusting patient engagement strategies and allocating resources accordingly.

Embodiments of the present disclosure relate to systems, methods, and user interfaces for providing intelligent touch care. More particularly, embodiments of the present disclosure utilizes contributing data elements in a community early warning score (CEWS) to predict touchpoint discipline and to recommend frequency, modality, and upstream transitions of care and outside service referrals for a patient in a community care setting. In response to a touch point (e.g., a change in condition or medication, a scheduled or unscheduled appointment, or a patient question), the CEWS can be utilized along with data in an EHR of a patient, data from a patient device, or data from a patient portal to initiate a follow-up (e.g., personal health question or encounter). Notification tools and scheduling functionality are provided via a user interface of the patient device to improve clinical workforce capacity, increase the number of patient touches, and encourage heightened patient engagement.