Pub Date : 2021-01-13eCollection Date: 2021-01-01DOI: 10.1177/2055102920987462
Håvard R Karlsen, Florian Matejschek, Ingvild Saksvik-Lehouillier, Eva Langvik
The aim of this paper is to summarise and evaluate the empirical support for the association between anxiety and cardiovascular disease (CVD) and to address challenges related to method and study design. We review results from meta-analyses and more recent findings on the association of anxiety and the risk of CVD. Depression and anxiety are often listed as psychosocial risk markers of CVD, but the role of anxiety as a risk factor for CVD has not received the same evidential support as the effects of depression. Through a narrative review we identified six meta-analyses as well as 15 recent large studies of anxiety and CVD that we summarise. Some of the conflicting findings may be artefacts of study design or population the sample is drawn from. Researchers should take care to be population specific, measurement specific and outcome specific, and to control for comorbid depression.
{"title":"Anxiety as a risk factor for cardiovascular disease independent of depression: A narrative review of current status and conflicting findings.","authors":"Håvard R Karlsen, Florian Matejschek, Ingvild Saksvik-Lehouillier, Eva Langvik","doi":"10.1177/2055102920987462","DOIUrl":"10.1177/2055102920987462","url":null,"abstract":"<p><p>The aim of this paper is to summarise and evaluate the empirical support for the association between anxiety and cardiovascular disease (CVD) and to address challenges related to method and study design. We review results from meta-analyses and more recent findings on the association of anxiety and the risk of CVD. Depression and anxiety are often listed as psychosocial risk markers of CVD, but the role of anxiety as a risk factor for CVD has not received the same evidential support as the effects of depression. Through a narrative review we identified six meta-analyses as well as 15 recent large studies of anxiety and CVD that we summarise. Some of the conflicting findings may be artefacts of study design or population the sample is drawn from. Researchers should take care to be population specific, measurement specific and outcome specific, and to control for comorbid depression.</p>","PeriodicalId":55856,"journal":{"name":"Health Psychology Open","volume":"8 1","pages":"2055102920987462"},"PeriodicalIF":1.7,"publicationDate":"2021-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809320/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38854669","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
This review examines the factors that affect the decision-making process of parental couples evaluating prenatal screening and diagnostic tests. A systematic search was performed using PubMed and PsycInfo databases. The 46 included studies had to: investigate the decision-making process about prenatal testing; focus on tests detecting trisomy 21, 18, 13, and abnormalities of sex chromosomes; be published in English peer-reviewed journals. The decision-making process seems composed of different levels: an individual level with demographic, clinical, and psychological aspects; a contextual level related to the technical features of the test and the information received; a relational level involving family and society.
{"title":"Decision-making factors in prenatal testing: A systematic review.","authors":"Valentina Di Mattei, Federica Ferrari, Gaia Perego, Valentina Tobia, Fabio Mauro, Massimo Candiani","doi":"10.1177/2055102920987455","DOIUrl":"https://doi.org/10.1177/2055102920987455","url":null,"abstract":"<p><p>This review examines the factors that affect the decision-making process of parental couples evaluating prenatal screening and diagnostic tests. A systematic search was performed using PubMed and PsycInfo databases. The 46 included studies had to: investigate the decision-making process about prenatal testing; focus on tests detecting trisomy 21, 18, 13, and abnormalities of sex chromosomes; be published in English peer-reviewed journals. The decision-making process seems composed of different levels: an individual level with demographic, clinical, and psychological aspects; a contextual level related to the technical features of the test and the information received; a relational level involving family and society.</p>","PeriodicalId":55856,"journal":{"name":"Health Psychology Open","volume":"8 1","pages":"2055102920987455"},"PeriodicalIF":2.9,"publicationDate":"2021-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/2055102920987455","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38854670","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-10-20eCollection Date: 2020-07-01DOI: 10.1177/2055102920967236
Nguyen Hoang Lan, Nguyen Thi Thu Thuy
This cross-sectional study is to examine the prevalence of depression and associated factors among 110 ethnic minority elderly in Kon Tum city, Vietnam. Depression was assessed using 30-items Geriatric Depression Scale. Multivariate linear regression analysis was employed to identify factors associated with depression. The prevalence of depression among participants was 25.5%. All were classified as mild depression level. Depression was significantly associated with age, gender, educational level, chronic diseases, stressful life events in the past 12 months, and family history of depression. These risk factors can help formulate effective public health programs to improve mental health among ethnic minority elderly.
{"title":"Depression among ethnic minority elderly in the Central Highlands, Vietnam.","authors":"Nguyen Hoang Lan, Nguyen Thi Thu Thuy","doi":"10.1177/2055102920967236","DOIUrl":"10.1177/2055102920967236","url":null,"abstract":"<p><p>This cross-sectional study is to examine the prevalence of depression and associated factors among 110 ethnic minority elderly in Kon Tum city, Vietnam. Depression was assessed using 30-items Geriatric Depression Scale. Multivariate linear regression analysis was employed to identify factors associated with depression. The prevalence of depression among participants was 25.5%. All were classified as mild depression level. Depression was significantly associated with age, gender, educational level, chronic diseases, stressful life events in the past 12 months, and family history of depression. These risk factors can help formulate effective public health programs to improve mental health among ethnic minority elderly.</p>","PeriodicalId":55856,"journal":{"name":"Health Psychology Open","volume":"7 2","pages":"2055102920967236"},"PeriodicalIF":1.7,"publicationDate":"2020-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/35/65/10.1177_2055102920967236.PMC8851141.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10265427","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-06-30eCollection Date: 2020-01-01DOI: 10.1177/2055102920935747
Pham Thi Lan Chi, Vu Thi Hoang Lan, Nguyen Hanh Ngan, Nguyen Thuy Linh
This study is conducted to learn about experiences and practices to cope with cyberbullying among high school students in Hanoi and to explore the association between the average time of Internet used per day among high school students in Hanoi, Vietnam, and the risk of being cyberbullied. A total of 215 students aged 13-18 years completed an online survey using respondent-driven sampling method. The experience of being cyberbullied was examined using the modified Patchin and Hinduja's scale. The prevalence of experiencing at least one type of cyberbullying was 45.1%. The most common type of cyberbullying was being called by names/made fun of. The average daily time spent on Internet showed dose-response association with the risk of being cyberbullied. The prevalence of having experienced cyberbullying was 54% among subjects who used Internet >3 hours/day compared to 39% among those who used 1-3 hours and 30% among those who used <1 hour. In terms of practices to cope with this, most students chose to ignore it and not share information with their family or teacher. The most frequent method to overcome this problem was talking with friends (60.8%). Research shows that the prevalence of cyberbullying victimization in Hanoi was high, and student's practices to cope with this new form of bullying were not efficient. Online time had dose-response association with risk of cyberbullying. More attention is needed to increase level of society/school awareness to prevent cyberbullying in Hanoi.
{"title":"Online time, experience of cyber bullying and practices to cope with it among high school students in Hanoi.","authors":"Pham Thi Lan Chi, Vu Thi Hoang Lan, Nguyen Hanh Ngan, Nguyen Thuy Linh","doi":"10.1177/2055102920935747","DOIUrl":"https://doi.org/10.1177/2055102920935747","url":null,"abstract":"<p><p>This study is conducted to learn about experiences and practices to cope with cyberbullying among high school students in Hanoi and to explore the association between the average time of Internet used per day among high school students in Hanoi, Vietnam, and the risk of being cyberbullied. A total of 215 students aged 13-18 years completed an online survey using respondent-driven sampling method. The experience of being cyberbullied was examined using the modified Patchin and Hinduja's scale. The prevalence of experiencing at least one type of cyberbullying was 45.1%. The most common type of cyberbullying was being called by names/made fun of. The average daily time spent on Internet showed dose-response association with the risk of being cyberbullied. The prevalence of having experienced cyberbullying was 54% among subjects who used Internet >3 hours/day compared to 39% among those who used 1-3 hours and 30% among those who used <1 hour. In terms of practices to cope with this, most students chose to ignore it and not share information with their family or teacher. The most frequent method to overcome this problem was talking with friends (60.8%). Research shows that the prevalence of cyberbullying victimization in Hanoi was high, and student's practices to cope with this new form of bullying were not efficient. Online time had dose-response association with risk of cyberbullying. More attention is needed to increase level of society/school awareness to prevent cyberbullying in Hanoi.</p>","PeriodicalId":55856,"journal":{"name":"Health Psychology Open","volume":"7 1","pages":"2055102920935747"},"PeriodicalIF":2.9,"publicationDate":"2020-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/2055102920935747","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38144530","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-06-26eCollection Date: 2020-01-01DOI: 10.1177/2055102920933073
Alessia Renzi, Michela Di Trani, Luigi Solano, Elisa Minutolo, Renata Tambelli
Infertility is a deeply distressing experience, which can threaten important personal and martial goals, frequently affecting the psychophysical health. A supportive relationship and a secure romantic attachment appear to reduce infertility stress, as well as play a relevant role in the success of assisted reproductive technology treatments. The principal aim of the study is to investigate the predictive effect of romantic attachment, couple characteristics, quality of life and age on assisted reproductive technology outcome. A total of 88 infertile women, enrolled in an assisted reproductive technology Centre of Rome, completed the Experience in Close Relationship-Revised, the Couple Relationship Inventory, the Fertility Quality of Life and a socio-demographic questionnaire. The participants completed the questionnaires at the beginning of the medical treatment. Data analyses showed significant associations among Experience in Close Relationship-Revised dimensions, Couple Relationship Inventory and Fertility Quality of Life Scales. Assisted reproductive technology outcome was negatively correlated to Experience in Close Relationship-Revised Avoidance and positively related to Couple Relationship Inventory Dependence. A multi-variable logistic regression revealed that Experience in Close Relationship-Revised Avoidance decreased the probability of pregnancy. The present findings partially confirmed the study hypotheses since several associations among couple characteristics, attachment anxiety and avoidance dimensions, infertility-related quality of life in infertile women were found. Furthermore, according to a definition of Avoidance, assisted reproductive technology positive outcome appears to be associated to lower levels of fear of dependence and interpersonal intimacy, and to a low need both for self-reliance and for reluctance to self-disclose within the romantic relationship. Further investigations are needed both to confirm this preliminary finding and for promoting focused therapeutic interventions for couples facing assisted reproductive technology.
{"title":"Success of assisted reproductive technology treatment and couple relationship: A pilot study on the role of romantic attachment.","authors":"Alessia Renzi, Michela Di Trani, Luigi Solano, Elisa Minutolo, Renata Tambelli","doi":"10.1177/2055102920933073","DOIUrl":"https://doi.org/10.1177/2055102920933073","url":null,"abstract":"<p><p>Infertility is a deeply distressing experience, which can threaten important personal and martial goals, frequently affecting the psychophysical health. A supportive relationship and a secure romantic attachment appear to reduce infertility stress, as well as play a relevant role in the success of assisted reproductive technology treatments. The principal aim of the study is to investigate the predictive effect of romantic attachment, couple characteristics, quality of life and age on assisted reproductive technology outcome. A total of 88 infertile women, enrolled in an assisted reproductive technology Centre of Rome, completed the Experience in Close Relationship-Revised, the Couple Relationship Inventory, the Fertility Quality of Life and a socio-demographic questionnaire. The participants completed the questionnaires at the beginning of the medical treatment. Data analyses showed significant associations among Experience in Close Relationship-Revised dimensions, Couple Relationship Inventory and Fertility Quality of Life Scales. Assisted reproductive technology outcome was negatively correlated to Experience in Close Relationship-Revised Avoidance and positively related to Couple Relationship Inventory Dependence. A multi-variable logistic regression revealed that Experience in Close Relationship-Revised Avoidance decreased the probability of pregnancy. The present findings partially confirmed the study hypotheses since several associations among couple characteristics, attachment anxiety and avoidance dimensions, infertility-related quality of life in infertile women were found. Furthermore, according to a definition of Avoidance, assisted reproductive technology positive outcome appears to be associated to lower levels of fear of dependence and interpersonal intimacy, and to a low need both for self-reliance and for reluctance to self-disclose within the romantic relationship. Further investigations are needed both to confirm this preliminary finding and for promoting focused therapeutic interventions for couples facing assisted reproductive technology.</p>","PeriodicalId":55856,"journal":{"name":"Health Psychology Open","volume":"7 1","pages":"2055102920933073"},"PeriodicalIF":2.9,"publicationDate":"2020-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/2055102920933073","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38128659","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-06-01eCollection Date: 2020-01-01DOI: 10.1177/2055102920920312
Caterina Gozzoli, Amalia De Leo
This study focuses on the experiences of professionals working with refugees and asylum seekers in the North of Italy. In the last years, professionals who work in this sector have been exposed to an increasing risk of physical and emotional malaise because of the number of challenges they daily manage. A qualitative study has been conducted with the aim of exploring the resource and the fatigue factors of professionals, in relation to their state of well-being or discomfort. Eight focus groups with multi-professional teams were held in eight refugee centres, for a total of 28 professionals involved (16 males and 12 females). The results allowed the description of three different professional profile conditions: Fatigued, Idealizing and Engaged.
{"title":"Receiving asylum seekers: Risks and resources of professionals.","authors":"Caterina Gozzoli, Amalia De Leo","doi":"10.1177/2055102920920312","DOIUrl":"https://doi.org/10.1177/2055102920920312","url":null,"abstract":"<p><p>This study focuses on the experiences of professionals working with refugees and asylum seekers in the North of Italy. In the last years, professionals who work in this sector have been exposed to an increasing risk of physical and emotional malaise because of the number of challenges they daily manage. A qualitative study has been conducted with the aim of exploring the resource and the fatigue factors of professionals, in relation to their state of well-being or discomfort. Eight focus groups with multi-professional teams were held in eight refugee centres, for a total of 28 professionals involved (16 males and 12 females). The results allowed the description of three different professional profile conditions: Fatigued, Idealizing and Engaged.</p>","PeriodicalId":55856,"journal":{"name":"Health Psychology Open","volume":"7 1","pages":"2055102920920312"},"PeriodicalIF":2.9,"publicationDate":"2020-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/2055102920920312","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38040202","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Among 170 adults with sickle cell disease, we evaluated chronic pain impact and disability prevalence, assessed age and gender differences, and identified psychosocial predictors of chronic pain intensity and disability. Most participants had a high level of disability. Chronic pain intensity and disability were significantly associated with pain catastrophizing and chronic pain self-efficacy, and worsened with age. Further research is needed to confirm study findings and develop interventions, including palliative care approaches that address catastrophizing and disability, particularly for young women and middle-aged adults with sickle cell disease. Moreover, consistent clinical assessment of chronic pain and psychosocial health should be implemented.
{"title":"Prevalence and predictors of chronic pain intensity and disability among adults with sickle cell disease.","authors":"Nadine Matthie, Coretta Jenerette, Ashley Gibson, Sudeshna Paul, Melinda Higgins, Lakshmanan Krishnamurti","doi":"10.1177/2055102920917250","DOIUrl":"https://doi.org/10.1177/2055102920917250","url":null,"abstract":"<p><p>Among 170 adults with sickle cell disease, we evaluated chronic pain impact and disability prevalence, assessed age and gender differences, and identified psychosocial predictors of chronic pain intensity and disability. Most participants had a high level of disability. Chronic pain intensity and disability were significantly associated with pain catastrophizing and chronic pain self-efficacy, and worsened with age. Further research is needed to confirm study findings and develop interventions, including palliative care approaches that address catastrophizing and disability, particularly for young women and middle-aged adults with sickle cell disease. Moreover, consistent clinical assessment of chronic pain and psychosocial health should be implemented.</p>","PeriodicalId":55856,"journal":{"name":"Health Psychology Open","volume":"7 1","pages":"2055102920917250"},"PeriodicalIF":2.9,"publicationDate":"2020-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/2055102920917250","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37950524","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-04-27eCollection Date: 2020-01-01DOI: 10.1177/2055102920913239
Ida Galli, Roberto Fasanelli
The aim of this investigation is to examine the structure and the content of different social groups' representations of the human microbiome. We employed a non-probabilistic sample comprising two groups of participants. The first group (n = 244) included university students. The second group included lay people (n = 355). We chose a mixed-method approach. The data obtained were processed using IRaMuTeQ software. The results allow us to identify the anchoring and objectification processes activated by the two different groups of interviewees. The results could be useful to those in charge of implementing campaigns aimed at promoting health literacy.
{"title":"Public understanding of science and common sense: Social representations of the human microbiome among the expert and non-expert public.","authors":"Ida Galli, Roberto Fasanelli","doi":"10.1177/2055102920913239","DOIUrl":"https://doi.org/10.1177/2055102920913239","url":null,"abstract":"<p><p>The aim of this investigation is to examine the structure and the content of different social groups' representations of the human microbiome. We employed a non-probabilistic sample comprising two groups of participants. The first group (<i>n</i> = 244) included university students. The second group included lay people (<i>n</i> = 355). We chose a mixed-method approach. The data obtained were processed using IRaMuTeQ software. The results allow us to identify the anchoring and objectification processes activated by the two different groups of interviewees. The results could be useful to those in charge of implementing campaigns aimed at promoting health literacy.</p>","PeriodicalId":55856,"journal":{"name":"Health Psychology Open","volume":"7 1","pages":"2055102920913239"},"PeriodicalIF":2.9,"publicationDate":"2020-04-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/2055102920913239","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38040200","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-04-04eCollection Date: 2020-01-01DOI: 10.1177/2055102920913235
Sarah C Griffin, Allison B Williams, Scott G Ravyts, Samantha N Mladen, Bruce D Rybarczyk
Despite the mounting evidence linking loneliness with health, the mechanisms underlying this relationship remain obscure. This systematic review and meta-analysis on the association between loneliness and one potential mechanism-sleep-identified 27 relevant articles. Loneliness correlated with self-reported sleep disturbance (r = .28, 95% confidence interval (.24, .33)) but not duration, across a diverse set of samples and measures. There was no evidence supporting age or gender as moderators or suggesting publication bias. The longitudinal relationship between loneliness and sleep remains unclear. Loneliness is related to sleep disturbance, but research is necessary to determine directionality, examine the influence of other factors, and speak to causality.
{"title":"Loneliness and sleep: A systematic review and meta-analysis.","authors":"Sarah C Griffin, Allison B Williams, Scott G Ravyts, Samantha N Mladen, Bruce D Rybarczyk","doi":"10.1177/2055102920913235","DOIUrl":"https://doi.org/10.1177/2055102920913235","url":null,"abstract":"<p><p>Despite the mounting evidence linking loneliness with health, the mechanisms underlying this relationship remain obscure. This systematic review and meta-analysis on the association between loneliness and one potential mechanism-sleep-identified 27 relevant articles. Loneliness correlated with self-reported sleep disturbance (<i>r</i> = .28, 95% confidence interval (.24, .33)) but not duration, across a diverse set of samples and measures. There was no evidence supporting age or gender as moderators or suggesting publication bias. The longitudinal relationship between loneliness and sleep remains unclear. Loneliness is related to sleep disturbance, but research is necessary to determine directionality, examine the influence of other factors, and speak to causality.</p>","PeriodicalId":55856,"journal":{"name":"Health Psychology Open","volume":"7 1","pages":"2055102920913235"},"PeriodicalIF":2.9,"publicationDate":"2020-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/2055102920913235","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37830140","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-03-30eCollection Date: 2020-01-01DOI: 10.1177/2055102920913477
Anne Geard, Marit Kirkevold, Marianne Løvstad, Anne-Kristine Schanke
This study explores the processes that promote coping with abruptive life changes, often experienced as life before and after injury. The consept of meaning making, was used as theoretical framework for analysisthr. Family members of individuals with spinal cord and acquired brain injury participated in two focus groups three to twenty years post-injury. Data was analysed using thematic analyses. Two main themes were identified: drawing upon different coping strategies and balancing family needs against personal autonomy. Making sense of an altered situation was by keeping a positive outlook, making comparisons to worst cases, engagement in activities and making room for own needs. Thus, the study illistrates that life can continue in a good manner after adversities, but requires flexibility and adjustments.
{"title":"How do family members of individuals with spinal cord and acquired brain injuries make sense of their experiences: A qualitative study of meaning making processes.","authors":"Anne Geard, Marit Kirkevold, Marianne Løvstad, Anne-Kristine Schanke","doi":"10.1177/2055102920913477","DOIUrl":"https://doi.org/10.1177/2055102920913477","url":null,"abstract":"<p><p>This study explores the processes that promote coping with abruptive life changes, often experienced as life before and after injury. The consept of meaning making, was used as theoretical framework for analysisthr. Family members of individuals with spinal cord and acquired brain injury participated in two focus groups three to twenty years post-injury. Data was analysed using thematic analyses. Two main themes were identified: drawing upon different coping strategies and balancing family needs against personal autonomy. Making sense of an altered situation was by keeping a positive outlook, making comparisons to worst cases, engagement in activities and making room for own needs. Thus, the study illistrates that life can continue in a good manner after adversities, but requires flexibility and adjustments.</p>","PeriodicalId":55856,"journal":{"name":"Health Psychology Open","volume":"7 1","pages":"2055102920913477"},"PeriodicalIF":2.9,"publicationDate":"2020-03-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/2055102920913477","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37830141","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}