Cultural Health Moments: A Search Analysis During Times of Heightened Awareness to Identify Potential Interception Points with Digital Health Consumers

Year after year whenever someone who is considered “high profile” discovers that they have some sort of sickness or if they pass away due to a sickness, there seems to be a heightened interest in that person. At the same time however, there is a heightened awareness of the type of sickness that the person had. Finding the moments in which there is a heightened sense of awareness towards a specific topic can be something of high value to various agencies and organizations. The objective of this study was to explore the moments in which people start to do some initial search queries when there is a high-profile health moment. Once it is understood when this moment occurs, further research can be done to understand where the search behavior shifts to searches of awareness, signs, symptoms, and introspection over time.

The Place of Psychiatric Rehabilitation in New Zealand Communities

<p>Supported Residential Care Facilities (SRCF's) play a distinctive role in the integration of mental health consumers within host communities. Despite the vast quantity of research on the sociological impacts of discrimination against mental health consumers, such as societal and self stigmatisation, little to no research is conducted on the effects that the built environment have upon mental health consumers in SRCF's in New Zealand post deinstitutionalisation. This study examines the 23 existing SRCF's within the Wellington region, examining their socioeconomic context, city planning context, physical environment context and the built typology of these facilities. Each of these research subjects are examined to identify and understand the implications they have on the integration of mental health consumers within their host communities at three scales; host community, location and facility design. The findings and insight drawn from sociological literature and empirical research are summarised within the design guideline and tested through a design based case study. The conclusions of this research can be summarised as follows: 1. It is desirable for host communities to be socioeconomically diverse with an appropriate level of public and mental health amenities 2. It is advantageous for SRCF's to be located within the 'inner edge context,' promoting a diverse urban context, socioeconomic context, diverse planning context and safe pedestrian access to public amenities. 3.The facility design of SRCF's should promote a 'recovery oriented practice,' achieved partially through context specific 'integration programs'. The majority of SRCF's within the research sample are located within residential suburbs. This research identifies that SRCF's and facilities alike must be located within the 'inner edge context'. The findings are of particular usefulness to Wellington's SRCF's yet are also helpful in understanding and improving the built environment of SRCF's within New Zealand communities.</p>

The Place of Psychiatric Rehabilitation in New Zealand Communities

<p>Supported Residential Care Facilities (SRCF's) play a distinctive role in the integration of mental health consumers within host communities. Despite the vast quantity of research on the sociological impacts of discrimination against mental health consumers, such as societal and self stigmatisation, little to no research is conducted on the effects that the built environment have upon mental health consumers in SRCF's in New Zealand post deinstitutionalisation. This study examines the 23 existing SRCF's within the Wellington region, examining their socioeconomic context, city planning context, physical environment context and the built typology of these facilities. Each of these research subjects are examined to identify and understand the implications they have on the integration of mental health consumers within their host communities at three scales; host community, location and facility design. The findings and insight drawn from sociological literature and empirical research are summarised within the design guideline and tested through a design based case study. The conclusions of this research can be summarised as follows: 1. It is desirable for host communities to be socioeconomically diverse with an appropriate level of public and mental health amenities 2. It is advantageous for SRCF's to be located within the 'inner edge context,' promoting a diverse urban context, socioeconomic context, diverse planning context and safe pedestrian access to public amenities. 3.The facility design of SRCF's should promote a 'recovery oriented practice,' achieved partially through context specific 'integration programs'. The majority of SRCF's within the research sample are located within residential suburbs. This research identifies that SRCF's and facilities alike must be located within the 'inner edge context'. The findings are of particular usefulness to Wellington's SRCF's yet are also helpful in understanding and improving the built environment of SRCF's within New Zealand communities.</p>

Role of Diffusion and Socio-cognitive towards Intention to use Health Portal among Health Consumers in Malaysia

The paper aims to examine the critical success factors that influence the attitude of health consumers and their intention to use the national health portal (MyHEALTH Portal). The study was constructed from two behavioral models; Diffusion of Innovation and Theory of Reasoned Action. It utilized an online survey hosted on the official portal website with a convenience sampling technique of 223 respondents. Results showed complexity did not significantly contribute towards attitude, while trialability and relative advantage showed significant contributions. Meanwhile, attitude influenced health consumers' intention to use the portal, while subjective norms indicated otherwise. Keywords: Diffusion; socio-cognitive; health portal, health consumer eISSN: 2398-4287© 2021. The Authors. Published for AMER ABRA cE-Bs by e-International Publishing House, Ltd., UK. This is an open access article under the CC BYNC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). Peer–review under responsibility of AMER (Association of Malaysian Environment-Behaviour Researchers), ABRA (Association of Behavioural Researchers on Asians/Africans/Arabians) and cE-Bs (Centre for Environment-Behaviour Studies), Faculty of Architecture, Planning & Surveying, Universiti Teknologi MARA, Malaysia. DOI: https://doi.org/10.21834/ebpj.v6i17.2809

Developing resilience and promoting positive mental health strategies in university students

AimsSuicide is one of the leading causes of death in young people living in Australia, accounting for 7.3% of all deaths among individuals aged 15–19 years. Historically, high levels of suicide have been recorded in Australian university students. This project aims to develop and test a massive online course-program (MOOC) for university students, underpinned by literature and strength-based suicide prevention principles, building resilience and awareness of mental health promoting activities.MethodA scoping review of the literature was undertaken to explore the effectiveness of current suicide prevention programs for undergraduate university students, and the effective elements contributing to the success of these programs. Six electronic databases were searched to identify relevant literature. Further, mental health consumers and university students were involved in co-producing the content of the six modules of the ‘Talk-to-me' MOOC.ResultNine articles were included in the review, discussing four types of programs including; gatekeeping, education, promotional messaging and online consultation. It was apparent from this review that there is a significant dearth of interventions and programs currently available to reduce the risk of suicide among undergraduate students, with many of the programs having limited efficacy. Despite this, a number of program elements were identified as beneficial to preventing suicide among post-secondary students including upskilling of students, and improving resilience, and self-management. These findings and further consultation with mental health consumers and undergraduate university students underpinned the development of the content of the ‘Talk-to-me' MOOC which is tailored to meet the needs of university students. The MOOC contains six modules: Mental fitness; strategies to increase mental fitness; self-harm; suicidal behaviour in young adults; interventions for suicidal behaviour; and, gatekeeper interventions. Two case study senarios depicting mental health challenges commonly experienced by yound adults portraying appropriate crisis communication skills were developed and filmed complementing the six ‘Talk-to-me' modules.ConclusionOverall, studies included in the review provide evidence to suggest that preventative programs, incorporating an educational component may be effective to be used in the MOOC to improving help-seeking behaviours among post-secondary education students. Findings from this review have underpinned the development of the ‘Talk-to-Me' MOOC which was launched in March 2020. To date this MOOC has enrolled over 45,000 participants from over 150 countries, with the average age of users being 24 years. Collectively, this line of work highlights that MOOCs are an effective means of mental health promotion to young adults.

The Patient as a Mobile Health Care Consumer

Many believe that digital health will be a catalyst to enable health care to become more market-centric and consumer-driven. Indeed, the Covid-19 pandemic has essentially redefined the concept of “elective” procedures based almost entirely on patient preference and behaviors, much of which was unexpected. Although the concept of educated and empowered patient consumers paints a compelling vision, many fear the unintended consequences of removing or minimizing trusted caregiver guidance from the equation. What are the risks and unintended consequences of self-managed care? Will patients properly prioritize? Will the benefits, risks, and potential trade-offs be understood? How will fact be separated from hype, misinformation and confirmation bias? In this chapter the opportunities and hazards of patients as mobile health consumers are detailed with a specific focus on potential harms and corresponding mitigations.

Health Information Seeking Behaviors on Social Media During the COVID-19 Pandemic Among American Social Networking Site Users: Survey Study (Preprint)

BACKGROUND In recent years, medical journals have emphasized the increasingly critical role that social media plays in the dissemination of public health information and disease prevention guidelines. However, platforms such as Facebook and Twitter continue to pose unique challenges for clinical health care providers and public health officials alike. In order to effectively communicate during public health emergencies, such as the COVID-19 pandemic, it is increasingly critical for health care providers and public health officials to understand how patients gather health-related information on the internet and adjudicate the merits of such information. OBJECTIVE With that goal in mind, we conducted a survey of 1003 US-based adults to better understand how health consumers have used social media to learn and stay informed about the COVID-19 pandemic, the extent to which they have relied on credible scientific information sources, and how they have gone about fact-checking pandemic-related information. METHODS A web-based survey was conducted with a sample that was purchased through an industry-leading market research provider. The results were reported with a 95% confidence level and a margin of error of 3. Participants included 1003 US-based adults (aged ≥18 years). Participants were selected via a stratified quota sampling approach to ensure that the sample was representative of the US population. Balanced quotas were determined (by region of the country) for gender, age, race, and ethnicity. RESULTS The results showed a heavy reliance on social media during the COVID-19 pandemic; more than three-quarters of respondents (762/1003, 76%) reported that they have relied on social media at least “a little,” and 59.2% (594/1003) of respondents indicated that they read information about COVID-19 on social media at least once per week. According to the findings, most social media users (638/1003, 63.6%) were unlikely to fact-check what they see on the internet with a health professional, despite the high levels of mistrust in the accuracy of COVID-19–related information on social media. We also found a greater likelihood of undergoing vaccination among those following more credible scientific sources on social media during the pandemic (<i>χ</i>²₁₆=50.790; <i>φ</i>=0.258; <i>P</i><.001). CONCLUSIONS The findings suggest that health professionals will need to be both strategic and proactive when engaging with health consumers on social media if they hope to counteract the deleterious effects of misinformation and disinformation. Effective training, institutional support, and proactive collaboration can help health professionals adapt to the evolving patterns of health information seeking.