To Convince Patients to Share Data, Engage them in the Process (Essay Sample)

To Convince Patients to Share Data, Engage them in the Process Name Institutional Affiliation To Convince Patients to Share Data, Engage them in the Process The process of transforming care and service delivery in health care is a significant approach and is achievable through engaging patients. It is imperative to note that patient engagement entails tools, activities, and relationships by both patients and clinicians towards promoting the aspect of decision-making. Patients feel empowered when they are engaged in the process of clinical procedures and will be willing to share data that is essential in decision-making. As a result, this will enhance the quality of care, promote patient empowerment, and ease improved health care outcomes for patients since they are empowered. In addition, empowering patients is a valuable tool for providers to improve health care quality because patients readily share data and information about various aspects that is important to the entire process. Moreover, researchers should approach establishing patient engagement strategy in order to get data that is considerable to initiatives such as Cancer Moonshot. The patient engagement process entails the application ofpatient surveys to benchmark provider and patient readiness. Survey results are significant because they enhance the patient`s readiness to provide data that is critical in addressing various health conditions across the globe. Researchers play a critical role in promoting health care through analysis of data collected in relation to various issues within the health care system. Involving them on aspects such as previous researches and the significance of the research to be conducted is essential. Majority of researchers fail to collect adequate data from patientsregarding various health conditions because they do not involve patients in the research process.  Releasing control of the individuals who will get access to study information is another essential aspect. This is because research is a process that requires participation from all participants, and moderation at all times. For instance, M-CEITA has played a big role in helping providers and researchers get the most out of patient engagement. This implies that once patients are engaged in the activities of the providers or researchers, they develop the sense of readiness and value of the process. For instance, cancer research is essential towards creating awareness and medical innovations. However, this faces obstacles because patients are not involved in the process of research. Releasing control to get access of information from patients may not be followed by the expectations of a researcher if there is little engagement with the patient. Currently, there are little incentives for cancer patients to share their data because they are less engaged in the processes of research. It is imperative to note that incentives that promote patient participation will convince them to share information and data regarding various health conditions. These incentives include participating in health-related online social networks that offers a platform for patients to feel free and share dataregarding health conditions. Online social networks provide a conducive space that allows patients from various regions to adequately collect data from patients suffering from various health conditions. It is imperative to note that patients should be given the greenlight by researchers to approach aspects such as their experiences with the health conditions and how they are coping with medical interventions. In most cases, patients do not share dataregarding these conditions because they are limited to the findings of a researcher and their confidentiality. Markman stipulates that "patients should have the right to access and evaluate the results whether or notthey contribute their health information to a repository" (Dvorak 2016). Patient should have the right or opportunity to access and evaluate the results as it is a key aspect in their engagement and ensures they are fully engaged not only in the process of data sharing, but also the outcomes of the data collected. This is a critical aspect because most the patients will not share information, unless assured that the end results will be sharedwith them. The notion of patient engagement with the researcher is to make sure that the empowerment process is adequately implemented on the patients. When empowerment is highly approached, the end results will be high response and sharing information about health conditions such as cancer by patients.  Convincing patients about the benefits of data sharing is another important aspect. For instance, patientscan be informed on the benefits they are likely to make as a result of sharing data about various health conditions they are suffering from. Informing patients about the benefits of sharing data may include the value of developing more superior antibiotics and other medications. Through this, patients find the value of sharing information because it will benefit them. In addition, the researcher has to outline other benefits such as creating awareness in the society through various initiatives that will make sure cancer patients receive desirable care. This will help others in the community understand the significance of undertaking screening for cancer before the condition developes into fatal stages. Receiving decision support for healthcare and health management decisions is another aspect that researchers in the health care sector can u...