Social media and online health services: A health empowerment perspective to online health information

2014 ◽  
Vol 39 ◽  
pp. 404-412 ◽  
Author(s):  
Rita S. Mano
2013 ◽  
Vol 411-414 ◽  
pp. 110-114 ◽  
Author(s):  
Dan Dumbrell ◽  
Robert Steele

Traditional forms of health information dissemination have previously involved a few key organizations originating health-related information and disseminating this to clinicians and the community. This information was typically disseminated via private, formalized and non-digital interactions between health information sources (HIS) and clinicians and consumers. With the introduction of the Internet, Web-based health information dissemination led to some changes with greater availability of online health information. However the recent adoption and uptake of social media has led to many more parties, both organizations of varying types, and individuals, participating in public health information dissemination; and this has also led to new forms of sharing health-related information, particularly involving a greater role for individuals. In this paper we introduce empirical findings in relation to how organizations and individuals are now using social media for sharing health information, and from this suggest themes to describe the changes from traditional to contemporary health information dissemination, as well as the new emerging roles and forms of interaction for health information dissemination.


2019 ◽  
Author(s):  
Anne Helen Hansen ◽  
Tor Claudi ◽  
Eirik Årsand

BACKGROUND Despite the increasing prevalence of diabetes and the increasing use of eHealth, little is known about the association between provider-based health services and eHealth among people with diabetes. This is the second study in a project exploring the associations between the use of eHealth and the use of provider-based health services. OBJECTIVE The objective of this study was to investigate which eHealth services are used among out-of-hours (OOH) visitors with type 1 diabetes (T1D), and whether the use of eHealth (eg, apps, search engines, video services, and social media) was associated with the use of OOH services. We also wanted to investigate associations between anxiety, reassurance, and change in doctor-seeking behavior because of health information acquired from the Internet, and the use of OOH services. METHODS We used data from a 2018 email survey of members of the Norwegian Diabetes Association (18-89 years old). Respondents with T1D were eligible for analyses. Using descriptive statistics, we estimated the use of OOH services and eHealth. Using logistic regressions, we studied the associations between the use of OOH services and the use of eHealth, as well as associations between the use of OOH services and reported consequences of using Internet-based health information. RESULTS In the sample of 523 people with T1D (mean age 47 years), 26.7% (129/484) visited OOH services once or more during the previous year. Among the OOH visitors, search engines were used for health purposes by 86.7% (111/128), apps (health apps in general) by 63.6% (82/129), social media by 45.3% (58/128), and video services by 28.4% (36/127). The use of OOH services was positively associated with self-reported anxiety/depression (odds ratio [OR] 4.53, 95% CI 1.43-14.32) and with the use of apps (OR 1.73, 95% CI 1.05-2.85), but not with other types of eHealth. Those who had felt anxious based on information from the Internet were more likely to visit OOH services compared with those who had not felt anxious (OR 2.38, 95% CI 1.50-3.78). People who had decided to consult a doctor based on information from the Internet were more likely to visit OOH services (OR 2.76, 95% CI 1.64-4.66), compared to those who had not made such an Internet-based decision. CONCLUSIONS People with T1D were frequent users of OOH services, and the OOH visitors were frequent users of eHealth. The use of OOH services was positively associated with the use of health apps, with self-reported anxiety/depression, and with feeling anxious based on information from the Internet. Likewise, deciding to consult a doctor based on information from the Internet was positively associated with OOH visits. The use of eHealth seems to have a significant impact on people with T1D.


2016 ◽  
Vol 5 (4) ◽  
pp. 55
Author(s):  
Rita S. Mano

This study examines the factors associated with computer use for the self-management of health among individuals diagnosed with chronic diseases (CD) in Israel. We distinguish between: (1) access to online health information, and (2) use of online health services (OHS). A geographic representative sample comprising 2008 individuals was contacted. 1406 individuals (67.6%) reported using the computer for health concerns. Four conditions – heart, cancer, diabetes and hypertension – were identified (N = 225). Using a series of logit regression models it is shown that CD increases access to online health information (OHI) but its effect of use of OHS is specific to: (1) type of CD, i.e., heart condition, and (2) type of provided service, i.e., medical updates. These results indicate that while computer use increases the odds for higher empowerment this may not necessarily lead to higher use of OHS provided by the healthcare provider among individuals diagnosed with CD decreasing the likelihood for better self-management. Implications for health policy are discussed.


2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Seth C. Kalichman ◽  
Bruno Shkembi ◽  
Moira O. Kalichman ◽  
Lisa A. Eaton

Abstract Background SARS-CoV-2 infection (COVID-19) is potentially severe for individuals with compromised immune systems, including people living with HIV. Along with the direct health threats of COVID-19, there are disruptions to social relationships and health services resulting from mitigation efforts instituted by public health authorities. This study examined the relationship between trust in the government and trust in COVID-19 health information from the US CDC, state health departments, and social media on the experience of COVID-19 social and health services-related disruptions. Methods People living with HIV (N = 459) recruited through social media advertisements and chain referrals completed confidential surveys delivered through an online platform. Results Participants experienced high-levels of disruptions to social relationships and health services attributable to COVID-19 mitigation efforts. We also observed high-rates of inaccurate information and low-levels of trust in government and sources of COVID-19 information. Greater disruptions to social relationships were predicted by more concern about oneself and others contracting COVID-19, whereas disruptions to health services were predicted by greater concern for oneself contracting COVID-19, greater general medical mistrust, and less trust in information from the CDC. Conclusions Findings have implications for the necessity of rebuilding public trust in credible sources of health information and stepping up efforts to counter sources of inaccurate information.


2021 ◽  
Vol 5 (Supplement_1) ◽  
pp. 643-643
Author(s):  
Alison Tang ◽  
Jung Kwak ◽  
Bo Xie ◽  
Lu Xiao ◽  
Sucheta Lahiri ◽  
...  

Abstract Family caregivers of persons with dementia (PWDs) use social media to obtain and share health information. Yet relatively little is known about the types of information that these caregivers share. We address this gap by analyzing caregivers’ posts (N = 401) in two subreddits, r/Alzheimers and r/dementia, which represent two subgroups on the social media platform Reddit. Our research questions were as follows: (1) What are these caregivers’ main purposes in posting? (2) What types of health information do the caregivers exchange online? (3) What are the characteristics of online posts that receive the caregivers’ greatest attention? Content and correlational analyses revealed that over half of users (57%) posted regarding specific types of health information that they desired to seek and share, whereas the remaining users posted information for sharing only. The health information most commonly posted fell into the following three categories: psychosocial health information, information about patients’ daily care, and characteristics of health conditions. The more health information types that a post contained, the greater the number of people who participated in the subreddit discussions. Further research should examine how social media meet PWD caregivers’ needs for information support.


Author(s):  
Christopher C. Hood ◽  
Sarah Bougourd

Some online health information and services have the potential to mislead, confuse or create unnecessary anxiety and more should be done to help people find trustworthy health websites and use online health services safely and effectively, says a new report on the ethics of ‘personalised healthcare’ (Nuffield Council on Bioethics, 2010). In September 2008, the UK Nuffield Council on Bioethics established a Working Party to consider the ethical issues raised by developments in medical profiling and online medicine that promise more ‘personalised healthcare’. The resulting report, published in October 2010, makes a number of policy and practice recommendations for providers and users of e-health services. This article highlights the recommendations made in three of the report’s e-health case studies: online health information, online personal health records, and telemedicine.


2013 ◽  
Vol 12 (04) ◽  
pp. 1350032 ◽  
Author(s):  
Yong-Mi Kim

A growing number of people are seeking health information on the Internet. To meet demands, healthcare providers are increasingly disseminating information online. While online health information has enhanced the dissemination of health information and improved people's health-related knowledge, critics posit that such dissemination has widened knowledge disparities in health information and health benefits as a result. Drawing on existing studies, this study identified the main causes of such disparity, namely education, health literacy, computer self-efficacy (CSE) and usage of health-related social media. The finding showed that education resided at the centre of the disparity and impacted other elements. An interesting finding is although individuals possess high levels of CSE, the efficacy does not highly impact their health benefits, meaning that computer does not directly cause health information disparity but is the tool to promote health-related knowledge disparity.


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