The relation between perceived level of the instrumental support’s exchange and the patterns of internet using in men with mental disorders

2020 ◽  
Vol LII (2) ◽  
pp. 59-62
Author(s):  
Olga M. Boyko

Relevance of this work is determined by the fact that the exchange of the instrumental social support plays an importantrole in the prevention of lowering the level of the social adaptation in people with mental illness. Aimof this work is to study the relative different types of internet using and amount of instrumental support in people with mental illness. Material and methods.84men between 16 and 32years were interviewed through the questionnaires COPE, California social networks inventory, questionnaire to the pictures of the social networks, semi-structured questionnaire for internet-using research. Results.(1)Absence of social networks (sites) usage for contacting with people can reduce intensity of exchange of instrumental social support. (2)The lack of usage internet for contact with old friends has a negative impact on the exchange quality of instrumental social support. It can contribute to atrainedhelplessness. (3)Informational internet using can reduce a frequency of use of coping strategy - recourse to instrumental support, which can be related to a stronger sense of empowerment. (4) Entertaining use of Internet technologies can reduce a number of ineffective requests for practical help. Conclusion.Therefore, using of internet technologies is related to perception of own system of exchange of instrumental social support as more effective. It must be considered in programs of social rehabilitation for people with mental illness.

2011 ◽  
Vol 21 (1) ◽  
pp. 4-14 ◽  
Author(s):  
Rachel Forrester-Jones ◽  
John Carpenter ◽  
Pauline Coolen-Schrijner ◽  
Paul Cambridge ◽  
Alison Tate ◽  
...  

2020 ◽  
Vol 5 (1) ◽  
pp. 184-194
Author(s):  
Hui Lin ◽  
Shijuan Li

AbstractWith the development of Internet technology, online health forums have become indispensable for people who seek non-professional health support. This research focuses on the content posted by cancer patients and their relatives in online health forums and social networks to raise the following research questions: What is the overall view of the social support network in the online tumor community? What are the information behaviors of the online tumor community in different identities of users? How users interact in this community and build this network of social support? What are the topics users would like to share and talk about? What kinds of users could be the key users in this community? Method: Using the post and comment data of the Oncology Forum of Tianya Hospital in 2019, combined with social network analysis and word co-occurrence network analysis, the following conclusions are obtained: (1) There are some central points in the overall social support network, and there are central users consistent with other social networks. (2) Positive users are more likely to comment on others, and it is easier to get others’ comments, while negative users are more likely to share personal information and do not want to participate more in social interaction. (3) Users focus on posting emotional and emotional content in content sharing. Information-based social support information. The social support experience that this type of information brings to users can be positive and negative. (4) The most active group in the patients’ online health community, followed by the patients’ children. (5) The relationship between users and patients is diverse and there are two types of singularity. Users with diverse relationships are more likely to be commented on, and they are more willing to comment on users who also have diverse relationships.


2017 ◽  
Vol 38 (1) ◽  
pp. 3-26 ◽  
Author(s):  
Daan Duppen ◽  
Michaël C. J. Van der Elst ◽  
Sarah Dury ◽  
Deborah Lambotte ◽  
Liesbeth De Donder ◽  
...  

Increasingly, policymakers assume that informal networks will provide care for frail older people. While the literature has mainly discussed the role of the family, broader social networks are also considered to be important. However, these social networks can diminish in later life. This systematic review investigates whether the social environment increases the risk of frailty or helps to prevent it. Findings from 15 original studies were classified using five different factors, which denoted five dimensions of the social environment: (a) social networks, (b) social support, (c) social participation, (d) subjective neighborhood experience, and (e) socioeconomic neighborhood characteristics. The discussion highlights that the social environment and frailty are indeed related, and how the neighborhood dimensions and social participation had more consistent results than social support and social networks. Conclusively, recommendations are formulated to contemplate all dimensions of the social environment for further research examining frailty and community care.


Author(s):  
Valentina Hlebec ◽  
Maja Mrzel ◽  
Tina Kogovšek

Some studies (e.g., Kogovšek & Hlebec, 2008, 2009) have shown that the name generator and the role relation approaches to measuring social networks are to some extent comparable, but less so the name generator and the event-related approaches (Hlebec, Mrzel, & Kogovšek, 2009). In this chapter, the composition of the social support network assessed by both the general social support approach and the event-related approach (support during 15 major life events) is analyzed and compared. In both cases, the role relation approach is used. In addition, in both approaches a more elaborate (16 possible categories ranging from partner, mother, father, friend to no one) and a more simple (6 possible categories ranging from family member, friend, neighbor to no one) response format is applied and compared. The aim of the chapter is to establish, in a controlled quasi-experiment setting, whether the different approaches (i.e. the general social support and the event-related approach) produce similar social networks regardless of the response format (long vs. short).


2019 ◽  
Vol 33 (6) ◽  
pp. 948-965
Author(s):  
Megan Woods ◽  
Rob Macklin ◽  
Sarah Dawkins ◽  
Angela Martin

Workplace conditions and experiences powerfully influence mental health and individuals experiencing mental illness, including the extent to which people experiencing mental ill-health are ‘disabled’ by their work environments. This article explains how examination of the social suffering experienced in workplaces by people with mental illness could enhance understanding of the inter-relationships between mental health and workplace conditions, including experiences and characteristics of the overarching labour process. It examines how workplace perceptions and narratives around mental illness act as discursive resources to influence the social realities of people with mental ill-health. It applies Labour Process Theory to highlight how such discursive resources could be used by workers and employers to influence the power, agency and control in workplace environments and the labour process, and the implications such attempts might have for social suffering. It concludes with an agenda for future research exploring these issues.


2020 ◽  
pp. 136346152095262
Author(s):  
Abner Weng Cheong Poon ◽  
Maria Cassaniti ◽  
Michele Sapucci ◽  
Rosaleen Ow

Many studies show that carers of people with mental illness experience a negative impact on their wellbeing. Given the growing number of people relocating to Australia every year, there are limited studies examining the experience of carers of people with mental illness from culturally and linguistically diverse communities in Australia. Using cultural safety as a conceptual framework, this exploratory study recruited 14 carers of Chinese and Vietnamese heritage who were attending culturally and linguistically oriented support groups in Sydney, Australia. Standardised, validated scales were administered to measure carers’ wellbeing and knowledge of recovery. Structured interviews were conducted to understand carers’ perceived needs. Descriptive statistical and qualitative thematic analysis were used. Findings show that carers experienced social isolation and psychological distress, had multiple diverse needs and had a reasonably good understanding of recovery. Six themes were identified: i) obtaining information in own language; ii) attaining emotional support from support groups; iii) needing respite services to cope with caregiving responsibilities; iv) involvement in planning of treatment and care; v) migration process influencing caregiving, and; vi) cultural and transcultural factors influencing caregiving experience. Findings indicate that some carers might be experiencing some level of culturally unsafe practices in mainstream mental health services. Implications for support groups and mental health services are discussed.


Author(s):  
Holley A. Wilkin

When it comes to health and risk, “place” matters. People who live in lower-income neighborhoods are disproportionately affected by obesity and obesity-related diseases like heart disease, hypertension, and diabetes; asthma; cancers; mental health issues; etc., compared to those that live in higher-income communities. Contributing to these disparities are individual-level factors (e.g., education level, health literacy, healthcare access) and neighborhood-level factors such as the socioeconomic characteristics of the neighborhood; crime, violence, and social disorder; the built environment; and the presence or absence of health-enhancing and health-compromising resources. Social determinants of health—for example, social support, social networks, and social capital—may improve or further complicate health outcomes in low-income neighborhoods. Social support is a type of transaction between two or more people intended to help the recipient in some fashion. For instance, a person can help provide someone who is grieving or dealing with a newly diagnosed health issue by providing emotional support. Informational support may be provided to someone trying to diagnose, manage, and/or treat a health problem. Instrumental support may come in the help of making meals for someone who is ill, running errands for them, or taking them to a doctor’s appointment. Unfortunately, those who may have chronic diseases and require a lot of support or who otherwise do not feel able to provide support may not seek it due to the expectation of reciprocity. Neighborhood features can enable or constrain people from developing social networks that can help provide social support when needed. There are different types of social networks: some can enhance health outcomes, while others may have a more limiting or even a detrimental effect on health. Social capital results in the creation of resources that may or may not improve health outcomes. Communication infrastructure theory offers an opportunity to create theoretically grounded health interventions that consider the social and neighborhood characteristics that influence health outcomes. The theory states that every neighborhood has a communication infrastructure that consists of a neighborhood storytelling network—which includes elements similar to the social determinants of health—embedded in a communication action context that enables or constrains neighborhood storytelling. People who are more engaged in their neighborhood storytelling networks are in a better position to reduce health disparities—for example, to fight to keep clinics open or to clean up environmental waste. The communication action context features are similar to the neighborhood characteristics that influence health outcomes. Communication infrastructure theory may be useful in interventions to address neighborhood health and risk.


2019 ◽  
Vol 3 (Supplement_1) ◽  
pp. S564-S564
Author(s):  
Christine Mair ◽  
Kasey Knopp

Abstract Existing literature on “aging alone” focuses on potential lack of support to “kinless” older adults who do not have traditional family ties (e.g., child, spouse; Margolis & Verdery, 2018), as well as the ways in which childless or unpartnered older adults may construct non-kin networks of support (e.g., friendship; Djundeva et al., 2018; Mair, 2019). In addition, older men’s and women’s social networks vary, with women reporting more network growth than men and potentially lower family involvement (Schwartz & Litwin, 2018). Finally, patterns of support (e.g., family care, friend interactions) differ by country context. However, it is unknown if and how the social networks of older adults who lack traditional family ties may differ by gender, as well as what forms of cross-national variation exist in these patterns. Using data from the Survey of Health, Ageing and Retirement in Europe (SHARE, N=17 nations, N=53,247 adults aged 50+), we take advantage of a unique social support network module in this cross-national dataset to compare closeness, proximity, quality, and type of ties by gender among older childless and unpartnered men and women by country. Among those without traditional family ties, we find that older women may be advantaged in terms of social support compared to older men, but that this advantage varies by nation. We discuss the details and implications of these results regarding potential policy implications about the differential risks faced by older men and women who lack traditional family ties in various country contexts.


2016 ◽  
Vol 37 (8) ◽  
pp. 990-1011 ◽  
Author(s):  
Scott R. Beach ◽  
Richard Schulz ◽  
Rodlescia Sneed

Social support and social networks are important correlates of elder mistreatment. This study tests hypothesized associations between perceived social support, social network size, and financial exploitation (FE). A population-based survey of 903 older adults (60+) in Allegheny County (Pittsburgh, Pennsylvania) found that lower perceived social support and larger social networks were simultaneously associated with higher risk for FE since age 60, controlling for known risk factors. The same associations were found for FE in the last 6 months. Older adults with larger social networks combined with lower perceived social support were most likely to report FE. When it comes to the role of social relationships and risk for FE, “more may not always be better.” Encouragement to widen the social network by “making new friends” should be stressed less than making sure these new network members will truly be supportive of the older adult.


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