National Health IT Priorities for Research
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Public Health Informatics Profile Toolkit
Public Health Informatics Profile Toolkit Developing a Public Health Informatics Profile: A Toolkit for State and Local Health Departments to Assess their Informatics Capacity Developed By: The Minnesota Department of Health Supported by: The Public Health Informatics Institute & The Robert Wood Johnson Foundation Public Health Informatics Profile Toolkit Acknowledgements Developing a Public Health Informatics Profile: a Toolkit for State and Local Health Departments to Assess their Informatics Capacity The project was supported by the Robert Wood Johnson Foundation through an InformationLinks Grant to the Public Health Informatics Institute. The initial project (the Public Health Informatics Profile Assessment) was also funded by Robert Wood Johnson Foundation through their Common Ground grant program. The authors of the Public Health Informatics Toolkit wish to thank the many members of the Minnesota Department of Health for their time, their expertise, and for their contributions to the original Public Health Informatics Profile Assessment. Jennifer Ellsworth Fritz, Priya Rajamani, Martin LaVenture Minnesota Department of Health Principal Developers Bill Brand, Debra Robic Public Health Informatics Institute Editorial Reviewers For More Information Public Health Informatics Institute Visit www.phii.org Call toll-free (866)815-9704 E-mail [email protected] Minnesota Department of Health Visit www.health.state.mn.us/ehealth Call Priya Rajamani @ 651-201-4119 E-mail [email protected] Call Jennifer Ellsworth Fritz @ 651-201-3662 E-mail -
Benefits and Barriers for Adoption of Personal Health Records Brittany Vance Marshall University, [email protected]
Marshall University Marshall Digital Scholar Management Faculty Research Management, Marketing and MIS Spring 3-2015 Benefits and Barriers for Adoption of Personal Health Records Brittany Vance Marshall University, [email protected] Brent Tomblin Marshall University, [email protected] Jena Studney Marshall University Alberto Coustasse Marshall University, [email protected] Follow this and additional works at: http://mds.marshall.edu/mgmt_faculty Part of the Health and Medical Administration Commons, Health Information Technology Commons, and the Management Information Systems Commons Recommended Citation Vance, B., Tomblin, B., Studeny, J., & Coustasse A., (2015, March). Benefits nda barriers for adoption of personal health records. Paper presented at the 2015 Business and Health Administration Association Annual Conference, at the 51st Annual Midwest Business Administration Association International Conference, Chicago, IL. This Article is brought to you for free and open access by the Management, Marketing and MIS at Marshall Digital Scholar. It has been accepted for inclusion in Management Faculty Research by an authorized administrator of Marshall Digital Scholar. For more information, please contact [email protected]. BENEFITS AND BARRIERS FOR ADOPTION OF PERSONAL HEALTH RECORDS Brittany Vance, MS Alumni College of Business Marshall University Graduate College 100 Angus E. Peyton Drive South Charleston, WV 25303 Brent Tomblin, MS Alumni College of Business Marshall University Graduate College 100 Angus E. Peyton Drive South Charleston, WV 25303 Jana Studeny, RN-BC, MSHI, Alumni Healthcare Informatics Program College of Health Professions Marshall University One John Marshall Drive Huntington, WV 25755 [email protected] Alberto Coustasse, DrPH, MD, MBA, MPH – CONTACT AUTHOR Associate Professor College of Business Marshall University Graduate College 100 Angus E. -
Office for Research Procedure
OFFICE FOR RESEARCH PROCEDURE INFORMED CONSENT PROCEDURES & WRITING PARTICIPANT INFORMATION AND CONSENT FORMS FOR RESEARCH Purpose: To describe the procedures related to informed consent procedures and writing patient information consent forms (PICF). To ensure that Austin Health adheres to the legal and ethical responsibility of obtaining a valid and informed consent for research participants. Scope: All phases of clinical investigation of medicinal products, medical devices, diagnostics and therapeutic interventions and research studies. Staff this document applies to: Principal Investigators, Associate Investigators, Clinical Research Coordinators, other staff involved in research-related activities. State any related Austin Health policies, procedures or guidelines: Austin Health Clinical Policy – (Informed) Consent (To Diagnosis & Treatment) Policy Document No: 2179 Policy Overview: A valid and informed consent will be obtained and documented prior to Austin Health research commencing. Emergency research procedures will be undertaken in compliance with the Guardianship and Administration Act 1986. Summary: For consent to be valid, it must be: freely given; specific to the proposed research and/or intervention; given by a person who is legally able to consent. 1. Elements of Consent: A consent is valid if it is: a) Freely given. b) Specific to the proposed research and/or intervention; c) Given by a person who is legally able to consent. AH VMIA SOP No. 006 Disclaimer: This Document has been developed for Austin Health use and has been specifically designed for Austin Health circumstances. Printed versions can only be considered up-to-date for a period of one month from the printing date after which, the latest version should be downloaded from ePPIC. -
Health Data As a Global Public Good
Health Data Governance Summit Pre-read: Health Data as a Global Public Good 30 June 2021 Global public goods Health Data Governance Summit Pre-read: Health Data as a Global Public Good Health data as a global public good The ODI has been working with WHO for the past month, holding discussions with 23 stakeholders and analysing 56 documents "Starkly and powerfully, the COVID-19 pandemic illustrates how critical "Despite progress in recent years, high-quality data are not routinely data use, with a human face, is to protecting lives & livelihoods. The collected in all settings, major health challenges are not adequately crisis is a wake-up call. We must accelerate a shift in our data and monitored, and effective interventions are not directed to the right analytics abilities: To respond to COVID-19 and build back better, to people, at the right time and at the right place. This impacts policies drive the Decade of Action for the SDGs, to amplify climate action, to and programmes and consequently, the health of entire populations. promote gender equality, to protect human rights, to advance peace Similarly, in order to meet the shared SDG commitment to “leave no-one and security, and to accelerate UN Reform – for greater impact on the behind”, we need disaggregated data to ensure equitable health ground." outcomes. This means we must strengthen comprehensive data systems, UN Secretary-General collaborate with other sectors, and apply innovative digital technologies to collect, analyse and use data to make informed decisions and deliver impact." WHO Director-General 2 Global public goods Health Data Governance Summit Pre-read: Health Data as a Global Public Good What are global public goods? "Global public goods are goods… whose benefits cross borders and are global in scope." - WHO Bulletin 2003 In traditional economic terms, public goods are have two key attributes: "Global public goods (GPGs) provide benefits to people in both rich and ● They are non-exclusionary: No one can be excluded from using poor countries. -
Big Data in Health Care
A Series by 2016 From predicting disease and identifying targeted therapies and cures, to improving our overall quality of life, big data is transforming the way health care decisions are made and care is delivered. Big Data in Health Care is a recently published series of articles that brings you the stories behind the research and celebrates researchers and organizations for their commitment to improving health care. Please accept this complimentary copy as our way of thanking you for your commitment to advancing medicine and improving patients’ lives. founding sponsor co-sponsor www.RealWorldHealthCare.org CONTENTS Big Data in Health Care Is Big Data Good for our Health? You Bet. Here’s Why. 3 Speaking with Dr. Phillip Bourne, National Institutes of Health. 8 Speaking with Dr. Hallie Prescott . 11 Closing the Healthcare Gap: The Critical Role of Non-Identified Information . 14 Real World Health Care Interview with Dr. Bonnie Westra. 17 Big Data Declares a War on Cancer . 21 Speaking with Dr. Clifford Hudis. 25 Is Big Data Good for our Health? You Bet. Here’s Why. By Cameron Warren and Merav Yuravlivker The term “Big Data” is increasingly used in our everyday lives. But each mention of it means something different, unique to what we use it for and how we interact with it. Big Data is not information. It’s the raw resource that people can use to discover new insights. Just as raw crude needs to be refined to run a car, Big Data needs to be refined to provide useful insights. In 2001, Doug Laney, who currently works for the analyst firm Gartner, defined this raw resource in terms of its three ubiquitous attributes, “the 3 V’s” – Volume, Velocity, and Variety. -
Informed Consent, AI Technologies, and Public Health Emergencies
future internet Review Trust, but Verify: Informed Consent, AI Technologies, and Public Health Emergencies Brian Pickering IT Innovation, Electronics and Computing, University of Southampton, University Road, Southampton SO17 1BJ, UK; [email protected] Abstract: To use technology or engage with research or medical treatment typically requires user consent: agreeing to terms of use with technology or services, or providing informed consent for research participation, for clinical trials and medical intervention, or as one legal basis for processing personal data. Introducing AI technologies, where explainability and trustworthiness are focus items for both government guidelines and responsible technologists, imposes additional challenges. Understanding enough of the technology to be able to make an informed decision, or consent, is essential but involves an acceptance of uncertain outcomes. Further, the contribution of AI- enabled technologies not least during the COVID-19 pandemic raises ethical concerns about the governance associated with their development and deployment. Using three typical scenarios— contact tracing, big data analytics and research during public emergencies—this paper explores a trust- based alternative to consent. Unlike existing consent-based mechanisms, this approach sees consent as a typical behavioural response to perceived contextual characteristics. Decisions to engage derive from the assumption that all relevant stakeholders including research participants will negotiate on an ongoing basis. Accepting dynamic negotiation between the main stakeholders as proposed here introduces a specifically socio–psychological perspective into the debate about human responses Citation: Pickering, B. Trust, but to artificial intelligence. This trust-based consent process leads to a set of recommendations for the Verify: Informed Consent, AI ethical use of advanced technologies as well as for the ethical review of applied research projects. -
RESEARCH STANDARD OPERATING PROCEDURES Documentation of Research Study Procedures in the Patients' Health Record
DEPARTMENT OF VETERANS AFFAIRS Research Service Policy Memorandum 11-42 South Texas Veterans Health Care System San Antonio, Texas 78229-4404 October 18, 2011 RESEARCH STANDARD OPERATING PROCEDURES Documentation of Research Study Procedures in the Patients' Health Record 1. PURPOSE: To describe the policies and procedures for the documentation of human research activities conducted at STVHCS in a patient's health record when a participant (research subject) is involved in a human research study. 2. POLICY: A research participant's health record includes the electronic medical record and any hard copy documentation located in Medical Records, combined, and is also known as the legal health record. Research files maintained by the Principle Investigators (PIs) and/or research staff are not part of the legal health record. A research record must be created or updated, and a progress note created, in the legal medical record when informed consent is obtained, a research visit has the potential to impact medical care (i.e. the research intervention may lead to physical or psychological adverse events), when the research requires use of any clinical resources (i.e. radiology, cardiology, pharmacy), or when a participant is disenrolled or terminated from a study. 3. ACTION: a. Documentation of the informed consent process (1) The PI or designated, trained study staff initiates the informed consent process with the use of the VA Form 10-1086 (lC document). (2) The IC document must be signed by (a) The participant or the participant's legally authorized representative (b) The person obtaining the informed consent (3) The PI or designated, trained study staff must enter a "Research ConsentiEnrollment Note" in the computerized patient record system (CPRS) after informed consent is obtained. -
Get the Facts About Telehealth
Get the Facts About Telehealth The COVID-19 pandemic has demonstrated that telehealth is a viable option for providing convenient, accessible and seamless care for patients. Myth #1: FACT: Data shows older patients are very comfortable with telehealth. Telehealth is In a survey conducted by Sutter Health, disease. More than 20% of Tera patients less feasible 52% of people aged 65 and older are aged 65 and above, allowing us reported having used telehealth during to quickly learn that telemedicine is for senior the pandemic and 93% of these patients welcome across any age range, disease citizens. reported having a positive experience. state and socioeconomic group. The key In addition, Sutter’s Tera Practice, factor for acceptance came down to a virtual-first medical practice that individuals experiencing firsthand Tera’s offers a whole ecosystem of healthcare convenience and responsiveness, and the support, has purposefully enrolled rapport they were able to build with their seniors who have at least one chronic personal care team virtually. OF SENIORS WHO USED TELEHEALTH 93% REPORTED A POSITIVE EXPERIENCE FACT: While more work needs to be done, Myth #2: telehealth is already improving critical access to care in rural and underserved communities. Telehealth Additional investments in technology, broadband and access are will amplify necessary to prevent the deepening of inequities and ensuring health widespread availability. Providers and policymakers must continue to work together to ensure the benefits of virtual care extend to our inequities. most vulnerable patients and that no community is left behind. Sutter serves millions of Medi-Cal patients in Northern California so this is a priority for our system. -
METHODS for REMOTE CLINICAL TRIALS Authors: Jennifer Dahne, Phd and Matthew J
METHODS FOR REMOTE CLINICAL TRIALS https://www.hrsa.gov/library/telehealth-coe-musc Authors: Jennifer Dahne, PhD and Matthew J. Carpenter, PhD Background Nearly all clinical trials are conducted locally, with recruitment limited to those who live proximal to a clinical trial site. These local trials struggle to recruit large, diverse, representative study samples. Consequently, many fail to meet their target enrollment and/or have unrepresentative samples. Trials that target specific subgroups of participants (e.g., low socioeconomic status, rural) or that address rare clinical conditions face even greater challenges, to the point where local trials may not even be feasible. Multi-site clinical trials can overcome some of these hurdles but incur their own unique challenges, most notably the need for sizable and costly infrastructure. With recent advances in telehealth and mobile health technologies, there is now a promising alternative: Remote clinical trials. Remote clinical trials (sometimes referred to as “decentralized clinical trials”) are led and coordinated by a local investigative team, but are based remotely, within a community, state, or nation. Such trials rely on remote methods to recruit participants into trials, consent study participants, deliver interventions, and maintain all follow-up assessments from a distance. Because participants are not required to attend in-person visits, remote trials improve sample representativeness, expand trial access, and enhance study feasibility[1, 2]. Remote clinical trials are now timelier in light of the Coronavirus Disease 2019 (COVID-19) global health pandemic, which has resulted in rapid requirements to shift ongoing clinical trials to remote delivery and assessment platforms. Indeed, guidance from numerous global health agencies now highlights that clinical trials procedures should shift, where possible, to alternative remote methods of delivery[3-5]. -
Perspectives on the Future of Personal Health Records
Perspectives on the Future of Personal Health Records June 2007 Perspectives on the Future of Personal Health Records Prepared for California HealthCare Foundation by Christopher J. Gearon Contributing Writers Michael Barrett, J.D. Patricia Flatley Brennan, R.N., Ph.D. David Kibbe, M.D., M.B.A. David Lansky, Ph.D. Jeremy Nobel, M.D., M.P.H. Daniel Sands, M.D., M.P.H. June 2007 About the Author Christopher J. Gearon is a freelance health and business writer in Silver Spring, Maryland. About the Foundation The California HealthCare Foundation, based in Oakland, is an independent philanthropy committed to improving California’s health care delivery and financing systems. Formed in 1996, our goal is to ensure that all Californians have access to affordable, quality health care. For more information about CHCF, visit us online at www.chcf.org. ISBN 1-933795-28-X ©2007 California HealthCare Foundation Contents 2 I Introduction 3 II. Background The PHR Market Business Models 6 III. Six Perspectives The Big-Picture Perspective The Consumer Perspective The Physician Perspective The Clinical Technology Perspective The Employer Perspective The Public Health Perspective 25 Endnotes I. Introduction The Internet and other information technologies have transformed American life in the last decade, empowering consumers and the way they work, bank, shop, and travel. However, a similar, long-anticipated transformation in health care has been elusive. Recent interest in a new kind of computerized medical record designed for consumers rather than health care providers could help speed this transformation. As a patient-centric hub of information and tools, personal health records (PHRs) have the potential to make the delivery of health care services more efficient and accessible, less costly, and safer. -
Security and Privacy for Mhealth and Uhealth Systems: a Systematic Mapping Study
Preprint submitted to IEEE Access. Date of current version June 22, 2020. Digital Object Identifier 10.1109/ACCESS.2017.DOI Security and Privacy for mHealth and uHealth Systems: a Systematic Mapping Study LEONARDO HORN IWAYA1,2, AAKASH AHMAD3, AND M. ALI BABAR.1,2 1Centre for Research on Engineering Software Technologies, The University of Adelaide, Adelaide, SA, Australia 2Cyber Security Cooperative Research Centre (CSCRC), Australia 3College of Computer Science and Engineering, University of Ha’il, Saudi Arabia Corresponding author: Leonardo Horn Iwaya (e-mail: [email protected]). The work has been supported by the Cyber Security Cooperative Research Centre (CSCRC) whose activities are partially funded by the Australian Government’s Cooperative Research Centres Programme. ABSTRACT An increased adoption of mobile health (mHealth) and ubiquitous health (uHealth) systems empower users with handheld devices and embedded sensors for a broad range of healthcare services. However, m/uHealth systems face significant challenges related to data security and privacy that must be addressed to increase the pervasiveness of such systems. This study aims to systematically identify, classify, compare, and evaluate state-of-the-art on security and privacy of m/uHealth systems. We conducted a systematic mapping study (SMS) based on 365 qualitatively selected studies to (i) classify the types, frequency, and demography of published research and (ii) synthesize and categorize research themes, (iii) recurring challenges, (iv) prominent solutions (i.e., research outcomes) and their (v) reported evaluations (i.e., practical validations). Results suggest that the existing research on security and privacy of m/uHealth systems primarily focuses on select group of control families (compliant with NIST800-53), protection of systems and information, access control, authentication, individual participation, and privacy authorisation. -
Dear Potential Research Participant, Thank You for Your Interest in This
Child Study Lab / Courtney A. Lewis UF-HSC PO Box 100165 Gainesville, FL 32610-016 Voice: (352) 273-5238 Dear Potential Research Participant, Thank you for your interest in this research study. This project is studying a brief format of Parent Child Interaction Therapy or PCIT. PCIT has been used for over 20 years and is a well established treatment for parents with young children who display problem behaviors such as aggression, disobedience, and hyperactivity. Traditionally parents work with their PCIT therapist for an average of 15 weeks. This study is examining a shorter version of PCIT. Parents who participate will be involved in the project for approximately 3 months. Below are brief descriptions of the screening, treatment, and follow-up phases included in this project. Screening Phase: The screening phase is a one week period where we collect information from you to see if our program would be a good fit for your family. During this phase you will answer questions about your child’s behavior, observe your child’s behavior at home, and come to the Child Study Lab located at UF/Shands for a 1.5 hour assessment. During this appointment you will review and complete a full informed consent. Treatment Phase: The treatment phase is divided into two parts. During the first part you and your child will attend five, two- hour therapy sessions. These will occur during a week-long period. During these sessions you will learn and practice skills to help playtime with your child be more calm and fun. We also will teach you effective discipline strategies.