Nicolson [ ]
25 randomised trials (involving 4788 participants) | Written material significantly improved knowledge of medicines in six of twelve trials. In three of these six trials recall of side effects also improved, but medicines recall significantly improved in only a minority of trials (one of four). | | | The results for attitudinal and behavioural outcomes were mixed. |
| | Comment: Overall, the authors concluded the combined evidence from this review is not sufficient to say whether written medicines information is effective in changing behaviours related to medicine taking. |
Foster [ ] | 17 randomised trials (involving 7442 participants) | Small (clinically insignificant) short-term improvements in pain, disability, fatigue and depression were found. |
| (Self management programmes run by lay people) | Positive effects on confidence to manage and self- rated health were also found. |
| | There was no effect on quality of life or use of health services. |
Interventions to facilitate communication and/or decision-making
Three interventions to facilitate communication and/or decision making that have been the focus of Cochrane systematic reviews are decision aids, personalised risk communication, and communication before consultations. Decision aids are a type of decision support intervention designed to help people make choices about health treatment options. Stacey (following O’Connor, who prepared the first Cochrane review), defines them as interventions containing ‘detailed, specific, and personalized information to help people focus on options and outcomes for the purpose of decision making’ [ 55 ]. They are important for decisions where there is uncertainty about a specific course of action. Personalised risk communication refers to the provision of information to consumers that is personally relevant to them. It is sometimes used to present and discuss the risks and benefits of healthcare in general, and of screening in particular, to consumers. As Edwards and colleagues outline, it can be based on a consumer’s own risk factors for a condition ( e.g. , their age) or calculated from their risk factors using epidemiological formulas. In the latter, the information is often presented as an absolute risk or as a risk score, or categorised into, for example, high-, medium-, or low-risk groups. Personalised risk communication may also be less detailed, for example, a listing of a consumer’s risk factors to guide discussion and intervention [ 56 ]. In their Cochrane review, Kinnersley and colleagues operationalise communication before consultations to include any intervention delivered before consultations, and which has been designed to help consumers (and/or their representatives) address their information needs within consultations [ 57 ].
Interventions to support behaviour change
One area that continues to challenge the Cochrane Consumers and Communication Review Group is the identification of effective interventions that support behaviour change. Four interventions which have been the focus of Cochrane reviews in this area are: interactive health communication applications; interventions to enhance medication adherence; contracts; and new methods of communication. Interactive health communication applications, defined by Murray and colleagues, are computer-based (usually web-based) information packages for patients that combine health information with at least one of: social support, decision support, or behaviour change support [ 58 ]. Interventions to enhance medication adherence include a wide range of single and multifaceted interventions; Haynes and colleagues identified: instruction, counseling, automated telephone monitoring and counseling, manual telephone follow-up, family intervention, increasing the convenience of care, simplified dosing, self-monitoring, reminders, special ‘reminder’ pill packaging, dose-dispensing units and medication charts, appointment and prescription refill reminders, reinforcement/rewards, medication formulations, crisis intervention, direct observation of treatments, lay health mentoring, comprehensive pharmaceutical care services, and psychological therapy in their Cochrane review [ 60 ]. Contracts refer to formalised (written or verbal) mutual agreements between two or more parties [ 61 ]. New methods of communication to date have included communicating DNA-based disease risk estimates to change health behaviours on lifestyle ( e.g. , smoking, physical activity, diet) [ 62 ] and providing consumers with a visual presentation ( i.e. , the source images) of their medical imaging ( i.e. , of magnetic resonance imaging, tomography, radiography, and/or ultrasonography) results to increase consumers’ engagement in health-related behaviours [ 63 ].
Interventions to inform and educate
Two interventions which have been the focus of Cochrane reviews to ‘inform and educate’ consumers are written information and self-management programmes. Written information is one of the most ubiquitous interventions targeting consumers [ 64 ].
Self management programmes have become a major initiative of government and community organizations in the area of chronic illness [ 65 ]. They promote various strategies for people to take an active approach to managing their health.
Effectiveness of knowledge translation strategies focusing on policy makers and senior health service managers
In contrast to the substantial evidence base on the effectiveness of knowledge translation strategies targeting healthcare professionals and consumers, few systematic reviews exist of interventions evaluating the effects of knowledge translation strategies for policy makers or senior health service managers. One review, conducted by Perrier and colleagues, evaluated interventions to increase the use of systematic reviews by health policy makers and managers [ 66 ]. Two studies were included in the review. The first study utilized a non-experimental design to report an intervention where public health policy makers were offered the opportunity to receive five relevant reviews. At three months and two years, respectively, 23% and 63% of respondents reported using at least one of the systematic reviews to make a policy decision. The second study was a randomised trial where health departments received one of three interventions: access to an online registry of systematic reviews, tailored messages plus access to the online registry of systematic reviews, or tailored messages plus access to the registry along with a knowledge broker who worked one-on-one with decision makers over a period of one year. While none of the interventions showed a significant effect on global evidence-informed decision making, tailored messages plus access to the online registry of systematic reviews showed a positive significant effect on public health policies and programs [ 66 ].
Lavis and colleagues conducted a systematic review of factors that influence the use of research evidence in public policy making [ 67 ]. Five criteria were used to assess validity of the included studies: the use of two or more data collection methods; a random or purposive sampling strategy; response rate >60%; two or more types of research use are examined; and two or more competing variables are examined.
A total of 16 studies met the criteria of using two or more data collection methods. These studies were conducted across a variety of jurisdictions, policy domains, content areas, and time periods. There was relatively little consistency in findings. However, two factors emerged with some frequency as being important to policy makers’ use of research evidence: interactions between researchers and policy makers in the context of policy networks such as formal advisory committees and in the context of informal relationships; and research that matched the beliefs, values, interests, or political goals and strategies of elected officials, social interest groups, and others. Both factors increased the prospects for research use by policy makers [ 67 ].
The findings from these reviews and other findings have led to the development of a number of knowledge translation approaches targeting policy makers and senior health services managers [ 28 , 68 , 69 ]. For example, a series of tools called SUPPORT Tools for evidence-informed health policy making (STP) were developed to assist policy makers in using research evidence. These tools were developed by members of the SUPporting POlicy relevant Reviews and Trials (SUPPORT) project, an international collaboration funded by the European Commission’s 6th Framework [ 70 ] ( http://www.supportcollaboration.org ). The SUPPORT tools describe a series of processes to help ensure that relevant research is identified, appraised and used appropriately by policy makers. The tools address four broad areas of interest related to policymaking: supporting evidence-informed policymaking [ 71 - 73 ]; identifying needs for research evidence in relation to clarifying problems, framing options, and planning implementation [ 74 - 76 ]; finding and assessing evidence from systematic reviews [ 77 - 79 ] and other kinds of evidence [ 80 , 81 ]; and moving from research evidence to decisions. The focus in this final area is on engaging stakeholders in evidence-informed policymaking [ 21 , 82 , 83 ] and on addressing how to use research evidence in decisions [ 84 - 86 ]. By focusing on how to ‘support’ the use of research evidence in health policymaking, the SUPPORT tools should increase the use of research evidence by policy makers [ 87 ] .
The SUPPORT tools describe a variety of packaging and push, facilitating pull, and exchange activities. Packaging and push activities focus on the activities of researchers to disseminate their research findings to a broad audience above and beyond traditional routes of dissemination such as publication in peer reviewed journals [ 11 ]. Examples of packaging and push activities include: increased emphasis on knowledge syntheses as the unit for knowledge translation; actionable messages; graded entry formats to allow the research user to access the level of detail that he or she requires (for example, the Canadian Health Services Research Foundation requires research reports to have one page of main messages, a three-page executive summary, and then no more than 25 pages for the complete project); using multiple communication channels tailored to the target audience; targeted electronic push of information relevant to the specific needs of research users—examples include the Contacts, Help, Advice and Information Network (C.H.A.I.N.) ([ 88 ], http://chain.ulcc.ac.uk/chain/ accessed 5 July 2011) and E-watch bulletin on Innovation in Health Services ( http://www.ohpe.ca/node/2740 accessed 5 July 2011); workshops and seminars with target audiences; and development of tools to help research users apply research findings in their own settings.
Facilitating pull activities focus on the needs of users, and creating an appetite for research results [ 11 ]. Pull activities include various training activities to improve policy makers’ and senior managers’ research literacy and interest. For example, the Canadian Health Services Research Foundation provides the EXTRA program to train senior healthcare executives in research application ( http://www.chsrf.ca/Programs/EXTRA.aspx accessed 5 July 2011). ‘One stop’ initiatives such as Health Systems Evidence also facilitate pull.
Exchange activities focus on building and maintaining new relationships between researchers and policy makers and senior managers to exchange knowledge and ideas [ 69 , 89 ]. For example, several research-funding programs require active participation of decision makers (sometimes including co-funding by healthcare organisations) in research teams. The rationale is that decision makers are more likely to consider research findings if they are actively involved in the research conducted in their settings to answer specific contextualized questions. These approaches legitimately focus on local knowledge translation of individual studies. However, the results of these studies should still be incorporated into systematic reviews to judge whether additional knowledge translation activities should be undertaken outside the context and relationships of the original study. Other exchange approaches include deliberative dialogues and the use of knowledge brokers to act as ‘human intermediaries’ between the world of research and action [ 69 , 82 , 90 ].
This profusion of approaches to improving knowledge translation to policy makers and senior healthcare managers highlights the increased recognition of the failure of traditional diffusion approaches to knowledge translation for this target group ( e.g. , [ 90 ]). Most of these approaches have a strong theoretical basis and face validity. However, it will be important to evaluate their benefits, harms and costs fully.
With what effect should research knowledge be transferred?
Appropriate endpoints of knowledge translation may vary across different stakeholder groups. For example, knowledge translation targeting policy makers and consumers should ensure that consideration of research evidence is a key component of their decision making, but recognize that there are other legitimate factors (for example, the policy context for policy makers, values and preferences of individual patients) that need to considered [ 91 - 93 ]. Thus, the resulting decision is likely to be evidence-informed but may not be particularly evidence-based. However, knowledge translation targeting professionals should result in practice that is more evidence-based and is likely to be observable as reflected in changes in professional behaviours and quality indicators.
In this paper, we have attempted to briefly summarise some of the key concepts and evidence about the effectiveness of knowledge translation activities targeting different stakeholder groups. We particularly recommend the five key questions developed by Lavis and colleagues as an aide for researchers and others involved in knowledge translation when developing knowledge translation activities [ 11 ]. There is a substantial (if incomplete) evidence base to guide choice of knowledge translation activities targeting healthcare professionals and patients. The evidence base on the effects of different knowledge translation approaches targeting healthcare policy makers and senior managers is much weaker but there are a profusion of innovative approaches that warrant further evaluation.
Grol observed that many current knowledge translation activities are based on participants’ beliefs, rather than evidence about the likely effectiveness of different approaches [ 94 ]. Grol challenged healthcare systems to develop and use a robust evidence base to support the choice of knowledge translation strategies, arguing, ‘evidence-based medicine should be complemented by evidence-based implementation.’ While we are some way from achieving this goal, there are grounds for optimism. Over the past twenty-five years, healthcare systems have invested heavily in knowledge synthesis activities that facilitate timely access of evidence. Further, it is possible to achieve clinically important practice changes by healthcare professionals and improved patient decision making with current knowledge translation activities.
Competing interests
MPE is Co-Editor in Chief and JMG and JNL are Editorial Board members of Implementation Science. All editorial decisions on this manuscript were made by another editor.
Authors’ contributions
JMG conceived of the idea of the paper. All authors contributed to writing the manuscript and approved the final version.
Acknowledgements
We are grateful to Egon Jonson for agreeing that we could use the chapter Grimshaw J, Eccles MP (2008). Knowledge Translation of Research Findings. In IHE Report June 2008: Effective Dissemination of Findings from Research. Institute of Health Economics, Alberta, Canada (2008) as the basis for this paper. JMG holds a Canada Research Chair. JES is a Postdoctoral Fellow funded by Canadian Institutes for Health Research. JMG and JNL are members and MPE is a member of the Scientific Advisory Board of KT Canada. Sophie Hill’s role as Coordinating Editor of Cochrane Consumers and Communication Review Group is supported by funding from the Quality, Safety and Patient Experience Branch, Department of Health Victoria, Australia and the National Health and Medical Research Council Funding for Australian-based Cochrane Collaboration Activities.
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This Biden Administration Proposal Just Might Salvage Your Credit Report
Published on Aug. 13, 2024
By: Dana George
- The Biden administration wants medical bills removed from credit reports to prevent lenders from making decisions based on medical information.
- Medical bills do not serve as a fair indicator of how likely someone is to pay their bills.
- Medical debt is the top reason for bankruptcies in the U.S.
Medical debt is no joke. Not only does the U.S. have the most expensive healthcare of any country, but medical debt is the No. 1 reason Americans file for bankruptcy, according to the American Medical Association (AMA).
Medical debt can also play havoc on a person's budget and personal finances, causing their credit score to plummet and making it harder for them to get credit when it's needed.
A step in the right direction
Two years ago, Experian, Equifax, and TransUnion -- the big three national credit reporting agencies -- announced that they were removing medical debts under $500 from credit reports. Removing relatively small medical debts certainly represented a step in the right direction for many U.S. consumers. Still, 15 million Americans were left with $49 billion worth of medical bills on their credit reports.
The Biden administration plan would force credit reporting agencies to go much further.
What this could mean for you
What matters is how erasing medical debt from credit reports will impact the everyday American. If your credit report currently lists medical expenses among your unpaid debts, here's how this change may benefit you.
Your credit score will get a boost
The Consumer Financial Protection Bureau (CFPB) estimates that Americans with medical debt on their credit reports will see their credit scores rise by an average of 20 points once medical debt is removed. A sudden 20-point boost may be just what some households need to qualify for a loan or open a credit card.
Your medical issues won't be public knowledge
While credit reports only show that you have outstanding medical debt and don't spell out the specifics, anyone who sees a copy of your report can tell that you (or someone in your household) have been ill.
That may not matter if you're applying for a car loan, but it could impact whether a potential employer checking your credit report decides to take a chance on you or a landlord believes you can pay your rent every month. In other words, it raises questions that should never be raised.
Your medical equipment cannot be repossessed
The proposed rule would prevent lenders from repossessing medical equipment like wheelchairs if you can't repay a loan.
Bill collectors can no longer use medical debt as a weapon
According to the CFPB, under the current system, medical debt collectors use the credit reporting system to force people to pay debts -- some of which they may not owe. CFPB reports that many debt collectors use a practice known as "debt parking."
Here's how it works: Debt collectors purchase medical debt at a discount. They then place the debt on your credit report, typically without your knowledge. It's only when you apply for credit that you discover that medical debt is holding you back from loan approval.
If you really need that loan, you may feel forced to pay the medical bill just to get it off your credit report and improve your credit score. Once medical debt no longer shows up on credit reports, bill collectors can no longer use this manipulative tactic.
This doesn't mean debt will be erased
There are undoubtedly benefits associated with having medical debts removed from your credit report, but you will still be responsible for repaying the debt . The point of removing the debt from your report is to make it easier for you to carry on with your financial responsibilities and get back on your financial feet.
The CFPB will continue to accept comments and feedback on the Biden administration proposal through Aug. 12, 2024. If all goes well, the rule will be finalized early next year.
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Our Research Expert
Dana is a full-time personal finance writer, with more than two decades of experience. Her focus is on helping readers feel less alone as they navigate their personal finances and offering actionable insights.
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This suggests a relatively recent increase in interest in the issue of knowledge transfer in health research. In the 79 articles were references to 88 models or frameworks (including multiple occurrences across articles), with 49 unique models/frameworks named and 13 models not explicitly named. ... BMC Medical Research Methodology, 6, 35 10. ...
Despite increasing interest in research on how to translate knowledge into practice and improve healthcare, the accumulation of scientific knowledge in this field is slow. Few substantial new insights have become available in the last decade. Various problems hinder development in this field. There is a frequent misfit between problems and approaches to implementation, resulting in the use of ...
Introduction. Failing to translate research knowledge into action in health care contributes to health inequities and wastes costly and time-consuming research 1-3.The gap between what is known and what is done leads not only to the under-use of effective treatments, but also to the incorrect use of treatments and the over-use of unhelpful or unproven treatments, all of which lead to negative ...
In this context, different terms are mainly used interchangeably. However, some studies used the terms knowledge transfer and knowledge diffusion to refer to the passive, untargeted, and unplanned spread of research findings, and the term knowledge dissemination for a more active spread, based on planned strategies (Graham et al. 2006; Nilsen ...
Some other commonly used terms are: knowledge translation, knowledge exchange, knowledge sharing, research utilization, implementation, dissemination, diffusion, continuing education, or continuing professional development (Graham et al. 2006). In the case of healthcare the term knowledge transfer is preferred because it indicates that the ...
One of the most consistent findings from clinical and health services research is the failure to translate research into practice and policy. For example, McGlynn and colleagues observed that patients in the USA received 55% of recommended care, and that quality varied by medical condition ranging from 79% of recommended care for senile ...
Knowledge translation (KT) is "the synthesis, exchange, and application of knowledge by relevant stakeholders to accelerate the benefits of global and local innovation in strengthening health systems and improving people's health" [].The process of KT ensures that evidence from research is used by relevant stakeholders, including healthcare providers, managers, policy-makers, informal ...
Empowering Knowledge Transfer in Healthcare. A Framework of Knowledge Transfer M ethods. Paul Kruse, Christian Kummer, Anja Jannack. 1 Knowledge Research Center e.V. 2 TU Dresden, Chair of ...
This collection aims to challenge so-called knowledge translation (hereinafter KT) in medicine and healthcare. The abbreviation 'KT' refers to a variety of scientific practices and research ...
Knowledge translation (KT) is a concept first used in 2000 by the Canadian Institute of Health Research (CIHR) ( 1 - 7) to address the gap between research knowledge and its application in clinical practice in health ( 1, 2, 4, 5 ). Since that time, use of the term has grown dramatically, with a tenfold increase revealed by a search of Medline ...
From Research to Practice: A Knowledge Transfer Planning Guide (2006) About this report: Authors: Rhoda Reardon, John Lavis, Jane Gibson. If you would like to receive a copy of this or any other of our reports, please contact us at: Institute for Work & Health 481 University Avenue, 8th Floor Toronto, Ontario M5G 2E9 416-927-2027 extension 2173.
Effective research transfer will ensure patients and populations benefit from evidence-based best practice. While there is an increasing rigor with which to approach research transfer in health care settings, greater demand among those responsible for research transfer for a more scientifically sound knowledge base will accelerate development of the discipline.
2.2 Medical knowledge transfer in OHCs. Knowledge transfer is the process of sharing or disseminating knowledge between two or more parties through a medium . Extant research classifies this knowledge transfer into explicit and tacit knowledge transfer and validates it on a variety of information system media .
explore possibilities to study knowledge transfer between disciplines by analysing cross-disciplinary citations in research literature. Part of this project was a comparison of age distributions of mono- and cross disciplinary citations, in which field specific differences were found between the speed of knowledge transfer within a discipline and
Background: Universities, public institutions, and the transfer of knowledge to the private sector play a major role in the development of medical technologies. The decisions of universities and public institutions regarding the transfer of knowledge impact the accessibility of the final product, making it easier or more difficult for consumers to access these products.
There is recognition in the CIHR definition that KT stages must consider coordinated communication, marketing, and training to facilitate KT. The seven stages are the following: Research priority setting. Research. Knowledge priority setting. Knowledge synthesis. Knowledge distribution and application. Use. Evaluation of uptake.
Knowledge transfer and exchange (KTE) is an interactive interchange of knowledge between research users and researcher producers (Kiefer et al. 2005).The primary purposes of KTE are to increase the likelihood that research evidence will be used in policy and practice decisions and to enable researchers to identify practice and policy-relevant research questions.
Pull activities and training: Such strategies can create an appetite for medical research and knowledge uptake. ... Closing the know-do gap in medical research is essential as failure to transfer research findings into practice contributes to more than $200 billion of wasted funding and poor health outcomes (Graham, Kothari & McCutcheon, 2018).
EVALUATING KNOWLEDGE TRANSFER IN NEURAL NETWORK FOR MEDICAL IMAGES Sina Akbarian, Laleh Seyyed-kalantari, Farzad Khalvati, and Elham Dolatabadi Abstract—Deep learning and knowledge transfer techniques have permeated the field of medical imaging and are consid-ered as key approaches for revolutionizing diagnostic imaging practices.
Background: With the rise of artificial intelligence (AI) in the field of dementia biomarker research, exploring its current developmental trends and research focuses has become increasingly important. This study, using literature data mining, analyzes and assesses the key contributions and development scale of AI in dementia biomarker research.
Sampling. This study aims to explore knowledge management practices within the research and development (R&D) sector of the information service industry, with a keen focus on companies operating ...
The search strategy included four search terms and their variations (knowledge (evidence, research, information, data), transfer (exchange, generation, translation, uptake, mobilization, dissemination, implementation), framework (model, concept) and health care (health system, health service, healthcare provider)) and was designed to be as ...
Background Patients from the lesbian, gay, bisexual, transgender, queer plus (LGBTQ +) community face various health inequalities and report poor healthcare experiences. Little is known about how knowledgeable and confident UK doctors are around LGBTQ + health, and previous research demonstrates that UK medical schools rarely deliver teaching in this area. This research evaluated the level of ...
In medical research, two types of knowledge transfer can be discerned. The first consists of the utilization of basic medical research for the "development of new methods for diagnosis, therapy, and prevention and their first testing in humans", while the second describes the "translation of results from clinical studies into everyday ...
The research methodology employed in this paper was limited to a case study, and the data utilized are not empirical data. ... Since the amount of knowledge transfer is an important aspect of the effectiveness of knowledge transfer, this paper constructs a Stackelberg game model with an innovation-quality-oriented threshold of the knowledge ...
Background Universities, public institutions, and the transfer of knowledge to the private sector play a major role in the development of medical technologies. The decisions of universities and public institutions regarding the transfer of knowledge impact the accessibility of the final product, making it easier or more difficult for consumers to access these products. In the case of medical ...
Muscle-specific kinase (MuSK) orchestrates establishment and maintenance of neuromuscular synapses, which enable muscle contraction. Autoantibodies targeting MuSK cause myasthenia gravis (MG), a disease characterized by fatigable skeletal muscle weakness which requires chronic immunosuppressive treatment and ventilatory support at some point in ~30% of patients. MuSK autoantibodies are ...
One of the most consistent findings from clinical and health services research is the failure to translate research into practice and policy. For example, McGlynn and colleagues observed that patients in the USA received 55% of recommended care, and that quality varied by medical condition ranging from 79% of recommended care for senile ...
Medical debt is no joke. Not only does the U.S. have the most expensive healthcare of any country, but medical debt is the No. 1 reason Americans file for bankruptcy, according to the American ...
To assess frequency, knowledge, attitude health behavior toward the risks and complication of cigarettes smoking and hookah in particular of Al-Kindy medical students. Materials and methods A cross-sectional study was conducted from December 2022 to April 2023 to assess frequency of Hookah smoking among 507 medical students at Al-Kindy Medical ...