186 research outputs found

    Help-seeking by male victims of domestic violence and abuse (DVA):a systematic review and qualitative evidence synthesis

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    ObjectivesTo understand help-seeking by male victims of domestic violence and abuse (DVA) and their experiences of support services by systematically identifying qualitative and mixed-method studies and thematically synthesising their findings.DesignSystematic review and qualitative evidence synthesis. Searches were conducted in 12 databases and the grey literature with no language or date restrictions. Quality appraisal of the studies was carried out using the Critical Appraisal Skills Programme tool. Reviewers extracted first and second order constructs related to help-seeking, identified themes and combined them by interpretative thematic synthesis.SettingDVA experienced by male victims and defined as any incident or pattern of incidents of controlling coercive or threatening behaviour, violence or abuse among people aged 18 or over who are or have been intimate partners or family members, regardless of gender or sexuality.ParticipantsMale victims of DVA.InterventionsAny intervention which provides practical and/or psychological support to male victims of DVA including but not limited to DVA-specific services, primary healthcare and sexual health clinics.Primary and secondary outcome measuresQualitative data describing help-seeking experiences and interactions with support services of male victims of domestic violenceResultsWe included twelve studies which were published between 2006 and 2017. We grouped nine themes described over two phases (a) barriers to help-seeking: fear of disclosure, challenge to masculinity, commitment to relationship, diminished confidence/despondency and invisibility/perception of services; and (b) experiences of interventions and support: initial contact, confidentiality, appropriate professional approaches and inappropriate professional approaches.ConclusionThe recent publication of the primary studies suggests a new interest in the needs of male DVA victims. We have confirmed previously identified barriers to help-seeking by male victims of DVA and provide new insight into barriers and facilitators to service provision.PROSPERO registration numberCRD42016039999

    Power and resistance: Reflections on the rhetoric and reality of using participatory methods to promote student voice and engagement in higher education

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    The focus of this article is methods for facilitating student voice and engagement in higher education, specifically participatory methods. Across the student voice and engagement literature there is a growing emphasis on promoting collaborative partnerships between staff and students. However, there is a lack of detail and criticality with regards to (1) exactly how genuine partnerships can be achieved and (2) comparing the vision for and the reality of positioning ‘students as partners’ in the current higher education climate. In this article, we evaluate the potential of participatory methods to facilitate quality partnerships between staff and students. Drawing on our experiences of being involved in a participatory project in one higher education institution, we offer reflective narratives from three different partners who participated in the project: student, lecturer and researcher. We use these narratives to explore the nature of the partnerships between lecturers and students, focusing specifically on issues of resistance and power. We conclude by considering the implications for how we conceptualise and implement student voice and engagement projects in higher education

    Making Socio-Ecological Art and Science Collaboration Work: A Guide

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    With global environmental challenges we are facing, such as the climate crisis and biodiversity loss, together with the role of ecosystems for human wellbeing, we can no longer rely on a singular disciplinary approach to address these challenges and the associated potential landscape change conflicts. In order to develop environmental strategies that encompass the social, economic and cultural, multi/ inter/trans-disciplinary approaches are required that seek inclusivity in sociocultural and intellectual terms. ‘The Arts’ is well placed to contribute to research and action that is inclusive and opens space for new imaginings and change. Artists and arts-based researchers have important knowledge and experiential contributions to make alongside those of natural and social scientists and the humanities. Research projects that include artists working alongside and in partnership with their natural and social science colleagues can build new perspectives and achieve a more holistic understanding of many socioecological issues. However, there is still a sense within the wider research community that bringing an arts perspective into applied research can be challenging, not least precisely because understanding what art is – and what art can contribute – is limited. This in turn leads to challenges when it comes to finding and commissioning artists. This guide to making socio-ecological art and science collaboration work sets out practical steps for finding and commissioning artists who have the appropriate skill sets and expertise. It has been written in response to the challenges and barriers faced by those not fully acquainted with art - its history, canons and current contemporary position - in commissioning artists to be a part of a research team. Arising through multiple conversations between researchers, artists and academics, the Guide aims to assist non-arts’ researchers incorporate arts based research and arts practice into multi and interdisciplinary research projects

    Using a socially-engaged arts approach to exploring how diverse socio-cultural groups accessed, valued, engaged with and benefited from an urban treescape during the COVID-19 Pandemic

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    This paper presents a socially-engaged arts approach to exploring the variety and specificity of cultural benefits urban park-users associated with its treescape during the COVID-19 pandemic. Drawing on the cultural ecosystem services framework, cultural benefits are understood in terms of positive impacts to ‘experiences’ (our relational interactions with the environment), ‘capabilities’ (our knowledge and abilities in relation to environmental interaction) and ‘identities’ (our perceptions of our relationship with the environment). The research captured evidence of a broad range of people’s interactions with the human and non-human world, whilst opening up an inclusive space for respondents to reflect on and share feelings about the significance of these experiences. The methods employed attracted a range of ‘quieter voices’ to participate, particularly more vulnerable park-users. They also attended to the multiple levels at which people connected with treescapes during this time, from less conscious material engagements to more emotionally and culturally driven transactions. This case study research highlights the important role of the park’s treescape in supporting people to feel better during the COVID-19 crisis and their cultural associations and ties to it. However, it also explores feelings of concern for and perceived lack of influence over this valued resource as potentially disbenefiting wellbeing. It identifies experiences of environmental anxiety, emerging from a lack of certainty over and agency within urban green spaces and treescapes and the benefits they can provide. It concludes that management of treescapes and greenspaces should be sensitive to impacts on environmental emotion

    ADHD in adults with recurrent depression

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    BACKGROUND: Depression is highly heterogeneous in its clinical presentation. Those with attention deficit/hyperactivity disorder (ADHD) may be at risk of a more chronic and impairing depression compared to those with depression alone according to studies of young people. However, no studies to date have examined ADHD in recurrently depressed adults in mid-life. METHOD: In a sample of women in mid-life (n=148) taken from a UK based prospective cohort of adults with a history of recurrent depression, we investigated the prevalence of ADHD and the association of ADHD with clinical features of depression. RESULTS: 12.8% of the recurrently depressed women had elevated ADHD symptoms and 3.4% met DSM-5 diagnostic criteria for ADHD. None of the women reported having a diagnosis of ADHD from a medical professional. ADHD symptoms were associated with earlier age of depression onset, higher depression associated impairment, a greater recurrence of depressive episodes and increased persistence of subthreshold depression symptoms over the study period, higher levels of irritability and increased risk of self-harm or suicide attempt. ADHD symptoms were associated with increased risk of hospitalisation and receiving non-first-line antidepressant medication. LIMITATIONS: ADHD was measured using a questionnaire measure. We focussed on mothers in a longitudinal study of recurrent depression, so the findings may not apply to males or other groups. CONCLUSIONS: Higher ADHD symptoms appear to index a worse clinical presentation for depression. Clinical implications include that in women with early onset, impairing and recurrent depression, the possibility of underlying ADHD masked by depression needs to be considered

    Following the children of depressed parents from childhood to adult life: A focus on mood and anxiety disorders

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    BACKGROUND: Parental depression increases risk for anxiety and depression in offspring. The transition from adolescence to adulthood is a common risk period for onset of such disorders. However, relatively few studies have considered development of these disorders from childhood to adulthood including multiple assessments during this transition period. METHOD: Offspring of depressed parents aged 9–17 years at baseline were followed prospectively for 13 years (n = 337). Average length of follow-up was 16 months between the first and second waves, 13 months between the second and third, and 8 years between the third and fourth. Current (3-month) psychopathology was assessed at each wave using diagnostic interviews. We derived estimates of 3-month prevalence, age at first diagnosis, course and comorbidity of disorders. Social functioning in adult life was assessed at the final wave and we assessed how prior and current disorder impacted adult functioning. RESULTS: A quarter of young people met criteria for a mood disorder and a third for anxiety disorder at least once. Mood and anxiety disorder prevalence increased from 4.5% and 15.8% respectively in childhood (9–11 years) to 22.3% and 20.9% respectively by age 23–28. Increased prevalence across the transition from adolescence to adulthood was particularly marked in males, while prevalence increased earlier in adolescence in females. Age at first diagnosis varied widely (mood disorder mean = 16.5 years (range 9–26); anxiety disorder mean = 14.5 years (range 9–28)). Over half (52%) reported functional impairment in early adulthood, 31% harmful alcohol use, and 10% self-harm or a suicide attempt. Both previous and current mood or anxiety disorder were associated with functional impairment in early adulthood. CONCLUSIONS: There is a prolonged risk period for mood and anxiety disorders in this group, with prevalence peaking in early adulthood. This highlights the need for prolonged vigilance and effective targeted interventions in the offspring of depressed parents

    Developing and validating a prediction model of adolescent major depressive disorder in the offspring of depressed parents

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    Background: Parental depression is common and is a major risk factor for depression in adolescents. Early identification of adolescents at elevated risk of developing major depressive disorder (MDD) in this group could improve early access to preventive interventions. Methods: Using longitudinal data from 337 adolescents at high familial risk of depression, we developed a risk prediction model for adolescent MDD. The model was externally validated in an independent cohort of 1,384 adolescents at high familial risk. We assessed predictors at baseline and MDD at follow‐up (a median of 2–3 years later). We compared the risk prediction model to a simple comparison model based on screening for depressive symptoms. Decision curve analysis was used to identify which model‐predicted risk score thresholds were associated with the greatest clinical benefit. Results: The MDD risk prediction model discriminated between those adolescents who did and did not develop MDD in the development (C‐statistic = .783, IQR (interquartile range) = .779, .778) and the validation samples (C‐statistic = .722, IQR = −.694, .741). Calibration in the validation sample was good to excellent (calibration intercept = .011, C‐slope = .851). The MDD risk prediction model was superior to the simple comparison model where discrimination was no better than chance (C‐statistic = .544, IQR = .536, .572). Decision curve analysis found that the highest clinical utility was at the lowest risk score thresholds (0.01–0.05). Conclusions: The developed risk prediction model successfully discriminated adolescents who developed MDD from those who did not. In practice, this model could be further developed with user involvement into a tool to target individuals for low‐intensity, selective preventive intervention

    Association between different methods of assessing blood pressure variability and incident cardiovascular disease, cardiovascular mortality and all-cause mortality : a systematic review

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    Dr Smith is supported by the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre (BRC). The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health. Dr Choon-Hian Goh is supported by the University of Malaya Post Doctoral Research Fellowship scheme. No funding was received to undertake the conduct of this study.Peer reviewedPostprin
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