scholarly journals Health Information–Seeking Behaviors of Family Caregivers: Analysis of the Health Information National Trends Survey (Preprint)

2018 ◽  
Author(s):  
Lauren R Bangerter ◽  
Joan Griffin ◽  
Kristin Harden ◽  
Lila J Rutten

BACKGROUND The growing population of aging adults relies on informal caregivers to help meet their health care needs, get help with decision making, and gather health information. OBJECTIVE The objective of this study was to examine health information–seeking behaviors among caregivers and to identify caregiver characteristics that contribute to difficulty in seeking health information. METHODS Data from the Health Information National Trends Survey 5, Cycle 1 (N=3181) were used to compare health information seeking of caregivers (n=391) with noncaregivers (n=2790). RESULTS Caregivers sought health information for themselves and others using computers, smartphones, or other electronic means more frequently than noncaregivers. Caregivers born outside of the United States reported greater difficulty seeking health information (beta=.42; P=.02). Nonwhite caregivers (beta =−.33; P=.03), those with less education (beta =−.35; P=.02), those with private insurance (beta =−.37; P=.01), and those without a regular health care provider (beta =−.35; P=.01) had less confidence seeking health information. Caregivers with higher income had more confidence (beta =.12; P≤.001) seeking health information. CONCLUSIONS This study highlights the prevalence of electronic means to find health information among caregivers. Notable differences in difficulty and confidence in health information seeking exist between caregivers, indicating the need for more attention to the socioeconomic status and caregivers born outside of the United States. Findings can guide efforts to optimize caregivers’ health information–seeking experiences.

2016 ◽  
Vol 12 (4) ◽  
pp. 863-876 ◽  
Author(s):  
Bradley Hiebert ◽  
Beverly Leipert ◽  
Sandra Regan ◽  
Jacquelyn Burkell

Beginning as early as 2009, recent shifts in Canadian health care delivery indicate that access to health information is essential to promote and maintain a healthy population. It is important to understand how and where various populations, such as underresourced rural populations, access health information so that public health agencies can develop and deliver appropriate information with, for, and in these contexts. There is a paucity of research that specifically examines how rural Canadian men seek health information; therefore, this review aimed to conceptualize this process based on three dynamic key constructs: health patterns of rural Canadians, health information–seeking behaviors, and rural gender identities. This conceptual theoretical literature review included 91 articles at the intersection of these three constructs. Discussion focuses on how residing in a rural region influences men’s health and health care access. Health information–seeking behaviors are discussed in terms of social networks and framed with a rural context. Connell’s theory of masculinity provides a useful approach to dissecting how rural men’s gender identities influence their health attitudes, and how such attitudes are embedded in rural social and cultural norms. Each major construct—health in rural Canada, health information seeking, and rural gender identities—is discussed to highlight how specific embodiments of masculinity may promote and inhibit men’s health information–seeking and positive health behaviors.


10.2196/15817 ◽  
2020 ◽  
Vol 22 (5) ◽  
pp. e15817 ◽  
Author(s):  
Zhaomeng Niu ◽  
Jessica Fitts Willoughby ◽  
Jing Mei ◽  
Shaochun Li ◽  
Pengwei Hu

Background Approximately 42.5 million adults have been affected by mental illness in the United States in 2013, and 173 million people have been affected by a diagnosable psychiatric disorder in China. An increasing number of people tend to seek health information on the Web, and it is important to understand the factors associated with individuals’ mental health information seeking. Identifying factors associated with mental health information seeking may influence the disease progression of potential patients. Objective This study aimed to test the planned risk information seeking model (PRISM) in China and the United States with a chronic disease, mental illness, and two additional factors, ie, media use and cultural identity, among college students. Methods Data were collected in both countries using the same online survey through a survey management program (Qualtrics). In China, college instructors distributed the survey link among university students, and it was also posted on a leading social media site called Sina Weibo. In the United States, the data were collected in a college-wide survey pool in a large Northwestern university. Results The final sample size was 235 for the Chinese sample and 241 for the US sample. Media use was significantly associated with mental health information–seeking intentions in the Chinese sample (P<.001), and cultural identity was significantly associated with intentions in both samples (China: P=.02; United States: P<.001). The extended PRISM had a better model fit than the original PRISM. Conclusions Cultural identity and media use should be considered when evaluating the process of mental health information seeking or when designing interventions to address mental health information seeking.


2018 ◽  
Vol 32 (1-2) ◽  
pp. 33-41 ◽  
Author(s):  
Takashi Yamashita ◽  
Anthony R. Bardo ◽  
Darren Liu ◽  
Phyllis A. Cummins

Objectives: Health literacy is often viewed as an essential skill set for successfully seeking health information to make health-related decisions. However, this general understanding has yet to be established with the use of nationally representative data. The objective of this study was to provide the first nationally representative empirical evidence that links health information seeking behaviors with health literacy among middle-age to older adults in the United States. Methods: Data were obtained from the 2012/2014 Program for the International Assessment of Adult Literacy (PIAAC). Our analytic sample is representative of adults age 45 to 74 years ( N = 2,989). Results: Distinct components of health literacy (i.e., literacy and numeracy) were uniquely associated with the use of different health information sources (e.g., health professionals, the Internet, television). Discussion: Findings should be useful for government agencies and health care providers interested in targeting health communications, as well as researchers who focus on health disparities.


2021 ◽  
Author(s):  
Gyeonghui Jeong ◽  
Hanna Choi

BACKGROUND The coronavirus disease (COVID-19) has also emerged as an infodemic, worsening the harm of the pandemic for people. The situation has highlighted the need for a deeply rooted understanding of health-information seeking behaviors (HISB). OBJECTIVE The aim of this paper is to review and provide insight regarding methodologies and the construct of content HISB surveys by answering the following research question: what are the characteristics of measurement tools for assessing HISBs in nationally representative surveys around the world? METHODS The Preferred Reporting Items for Systematic review and Meta-Analysis Protocols (PRISMA-P) was used as a framework for the study. A data search was performed through six international and two Korean search engines between October 22, 2017, and November 13, 2017. Initially, the studies performed among nationally representative samples within the past 10 years were included to discover HISB survey instruments. The methodologies of the studies using HISB surveys were analyzed. For content analysis, two researchers reached a consensus through discussion by scrutinizing the contents of each survey questionnaire. RESULTS A total of 10 survey tools from six countries were identified after a review of 1,476 records from the search results. Five survey tools (HINTS, HTS, ANHCS, NHIS, and HTHS) from the United States (U.S.) and each of one tool from European Union (E.U.), France, Germany, Israel, and Poland were identified. National institutes or individual researchers designed these surveys by using the items of the dichotomous or Likert scale. Telephone or online surveys were commonly used targeting the adult population (≥ 15 years of age). From the content analysis, the domains of the survey items were categorized as follows: health (overall health, lifestyle, and cancer), information (health information and patient medical records), and channel (offline and online). All categories encompassed behavioral and attitude dimensions. A theoretical framework—an Information-Channel-Health (ICH) structure—for HISB was proposed. CONCLUSIONS The results can contribute to the development and implementation of survey tools for HISB with integrated questionnaire items. This will help to understand HISB trends and enhance patient engagement in national healthcare.


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