Evaluation of Healthcare Avoidance Behavior Using the Healthcare National Trends Survey

2020 ◽  
Vol 30 (1) ◽  
Author(s):  
Yiu Ming Chan ◽  
Clauda Laster

As online search engines have become increasingly popular for people to use to locate necessary health information, the number of individuals choosing to avoid visiting a doctor is dramatically increasing. This study analyzed 2007 Health Information National Trends Survey (HINTS) data and found that people who avoid visiting a doctor were more likely to be male, younger, and less educated than those who do not avoid seeing a doctor. Also, individuals who have less health insurance coverage, have serious psychological distress (SPD), and suffered cancer information overload were more likely to report psychosocial barriers to care. Furthermore, the levels of trust of doctors and visiting a social networking site were significant predictors of “doctor avoidance.” In addition, individuals who felt their personal health information was not being safely guarded by doctors were more likely to avoid visiting a doctor. These findings can help healthcare professionals better understand the characteristics of persons who avoid visiting a doctor and professionals can use these conclusions to provide more effective ways to deliver health information to change healthcare behavior.

2009 ◽  
Vol 15 (1_suppl) ◽  
pp. 16-29
Author(s):  
Jiali Ye ◽  
Zhiheng Xu ◽  
Bamidele Adesunloye

Information seeking has significant impact on improving cancer preventive activities and health decision making. This study sought to compare Black and White adults on cancer information seeking and the choice of primary information sources. Non-Hispanic Black and non-Hispanic White adults completed Health Information National Trends Surveys (HINTS) collected in 2003 and in 2005. The results of bivariate analyses showed that Whites were more likely than Blacks to be cancer information seekers for both years (2003: 49.0% vs. 40.8%, p < .001; 2005: 54.6% vs. 46.9%, p = .008). However, after controlling for sociodemographic variables, race was not significantly associated with cancer information seeking. Both racial groups increased their likelihood of cancer information seeking from 2003 to 2005, although the increase was only statistically significant for Whites ( p < .001). Health providers and the Internet were the top two most selected primary cancer information sources for both racial groups. These findings indicate that sociodemographic factors, such as gender, education, and cancer history, may shape the racial difference in health information seeking among the general population. Among all the information sources, health care providers and the Internet play the most important role in providing cancer-related information.


2017 ◽  
Vol 76 (7) ◽  
pp. 853-868 ◽  
Author(s):  
Laura LB Barnes ◽  
Jam J Khojasteh ◽  
Denna Wheeler

Objective: This study aimed to identify predominant search patterns in a recent search for health information and a potential search for strongly needed cancer information, to identify the commonly scanned sources of information that may represent stable elements of the information fields characteristic of these patterns, and to evaluate whether search patterns are the same for cancer patients and non-patients. Design: Analysis of Health Information National Trends Survey 4 Cycle 2 (HINTS 4.2) data, a nationally representative survey administered by the US National Cancer Institute. Methods: The search patterns of individuals responding to survey questions about a recent search for health information and a hypothetical search for strongly needed cancer information were identified by cross-classifying the first source of information to be consulted in both search contexts. Using a mixed-model repeated-measures analysis of variance (ANOVA), we evaluated the relationship between search patterns and scanned sources of cancer information. Results: Five predominant search patterns or groups were evident: Internet–doctor (29%), Internet–Internet (25%), doctor–doctor (16%), Internet–cancer organisation (6%) and print–doctor (6%) for recent search and for the hypothetical search for strongly needed information, respectively. Patterns did not vary by presence/absence of cancer diagnosis. Information search groups differed both demographically and in the sources of information scanned. Patterns were replicated in data from two additional HINTS surveys which differed in the wording of the focal questions. Conclusion: Differences among the patterns in various health-related attitudes and behaviours are identified. Implications for patient engagement in shared decision-making, particularly in the presence of rapid developments in health information technology, are discussed.


Author(s):  
Sara R. Collins Collins ◽  
Cathy Schoen Schoen ◽  
David C. Radley Radley ◽  
Sophie Beutel Beutel

1994 ◽  
Vol 8 (3) ◽  
pp. 67-73 ◽  
Author(s):  
James M Poterba

This brief paper explores the likely effects of government-imposed global budget caps, such as those in the Clinton administration proposal, on health care spending. It argues that health reform proposals that guarantee universal access to a basic package of medical benefits create a substantial new constituency for higher health care outlays. Political and potential legal pressures to expand rather than limit the set of guaranteed benefits, coupled with an expansion of the number of individuals with health insurance coverage, make it unlikely that global budget targets will succeed in reducing the rate of health care spending growth.


2020 ◽  
Vol 29 (7) ◽  
pp. 1348-1356 ◽  
Author(s):  
Marlene Camacho-Rivera ◽  
Christopher J. Gonzalez ◽  
Jason Amilcar Morency ◽  
Kelly D. Blake ◽  
Rose Calixte

2006 ◽  
Vol 11 (sup001) ◽  
pp. 117-133 ◽  
Author(s):  
Linda Squiers ◽  
Mary Anne Bright ◽  
Lila J. Finney Rutten ◽  
Audie A. Atienza ◽  
Katherine Treiman ◽  
...  

2017 ◽  
Author(s):  
Onur Asan ◽  
Farion Cooper II ◽  
Sneha Nagavally ◽  
Rebekah J Walker ◽  
Joni S Williams ◽  
...  

BACKGROUND Emerging health technologies are increasingly being used in health care for communication, data collection, patient monitoring, education, and facilitating adherence to chronic disease management. However, there is a lack of studies on differences in the preference for using information exchange technologies between patients with chronic and nonchronic diseases and factors affecting these differences. OBJECTIVE The purpose of this paper is to understand the preferences and use of information technology for information exchange among a nationally representative sample of adults with and without 3 chronic disease conditions (ie, cardiovascular disease [CVD], diabetes, and hypertension) and to assess whether these preferences differ according to varying demographic variables. METHODS We utilized data from the 2012 and 2014 iteration of the Health Information National Trends Survey (N=7307). We used multiple logistic regressions, adjusting for relevant demographic covariates, to identify the independent factors associated with lower odds of using health information technology (HIT), thus, identifying targets for awareness. Analyses were weighted for the US population and adjusted for the sociodemographic variables of age, gender, race, and US census region. RESULTS Of 7307 participants, 3529 reported CVD, diabetes, or hypertension. In the unadjusted models, individuals with diabetes, CVD, or hypertension were more likely to report using email to exchange medical information with their provider and less likely to not use any of the technology in health information exchange, as well as more likely to say it was not important for them to access personal medical information electronically. In the unadjusted model, additional significant odds ratio (OR) values were observed. However, after adjustment, most relationships regarding the use and interest in exchanging information with the provider were no longer significant. In the adjusted model, individuals with CVD, diabetes, or hypertension were more likely to access Web-based personal health information through a website or app. Furthermore, we assessed adjusted ORs for demographic variables. Those aged >65 years and Hispanic people were more likely to report no use of email to exchange medical information with their provider. Minorities (Hispanic, non-Hispanic black, and Asian people) were less likely to indicate they had no interest in exchanging general health tips with a provider electronically. CONCLUSIONS The analysis did not show any significant association among those with comorbidities and their proclivity toward health information, possibly implying that HIT-related interventions, particularly design of information technologies, should focus more on demographic factors, including race, age, and region, than on comorbidities or chronic disease status to increase the likelihood of use. Future research is needed to understand and explore more patient-friendly use and design of information technologies, which can be utilized by diverse age, race, and education or health literacy groups efficiently to further bridge the patient-provider communication gap.


Sign in / Sign up

Export Citation Format

Share Document