138 research outputs found

    Resilience to change: understanding social-ecological dynamics in reef-dependent fishing communities in Madagascar

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    Coral reefs are located across the tropics, predominantly in developing countries where reef fisheries play an important role in generating income and supporting food security. These fisheries are increasingly governed in co-management arrangements, which typically involve a form of shared management authority between local resource users and a government or non-governmental partner. As coral ecosystems rapidly degrade, driven by climate change, overfishing and other anthropogenic impacts, effective co-management will be a critical pathway to secure a sustainable future for reef-dependant coastal communities. To support locally-relevant co-management strategies, a comprehensive understanding of the local social-ecological context is required – including the environmental conditions, resource dynamics and the social and cultural setting. In this context, co-management stakeholders are increasingly investigating how different types of data, including scientific monitoring, local ecological knowledge, and citizen-science data can be used to inform management decisions. However, this remains under investigated in the context of reef fisheries co-management. This thesis addresses this gap by studying the social and ecological dynamics of traditional Vezo fishing communities and coral reef fisheries in the Velondriake Locally Managed Marine Area (LMMA) in southwest Madagascar. The research draws on data collected over two decades including citizen science reef monitoring data (2012 -2018), social surveys conducted in 11 villages in 2016 and 2021, semi-structured and key informant interviews, participatory video and climate reanalysis data. The thesis contains four research chapters structured as research articles. The first chapter assesses the impact and recovery of the coral ecosystem following the damage caused by Cyclone Haruna in 2013. Using generalized linear model analysis, we found the damage was spatially heterogeneous throughout the study region and that the coral reef sites showed positive signs of recovery in the two years following the cyclone. However, a shift in dominant coral species from fragile to more resilient morphologies following the cyclone indicates that an increased frequency of destructive cyclones could cause a shift in the coral assemblage. The second chapter examines the dynamics of adaptive capacity— the capacity of individuals or groups to cope with change— in the communities of Velondriake. Adaptive capacity is found to be differentiated between social groups but relatively stable over time. The findings suggest that co-management interventions, such as livelihood programmes could improve adaptive capacity. However, findings indicate that only certain adaptive capacity indicators were significantly associated with impact and response from disturbance events, and these indicators differed between the type of disturbance. These findings underscore that caution is required when using adaptive capacity indicators in the absence of locally derived evidence of actual adaptive behaviour. The third chapter integrates local knowledge and scientific approaches to examine catch trends and climate variability and change in the Velondriake LMMA over the past generation. The study reveals a long-term decline in fin fish and octopus fisheries that aligns with socioeconomic pressures. Shifting wind patterns were identified as a key climate variable impacting fishers’ livelihoods. This chapter underscores the unequal impacts of declining catches on male and female fishers and disparities in adaptation options. The final research chapter is an investigation of how participatory video can be used as a tool to support co-management. Participatory video is found to be a means to synthesise local knowledge concerning shifting social and ecological conditions, fostering dialogue and action towards locally relevant management interventions. Collectively, the research in this thesis underscores the climate and ecological challenges faced by reef-dependent fishing communities and their ramifications on the social-ecological system in southwest Madagascar. It reveals differentiated resilience among community members to declining marine ecosystems and elucidates potential interventions that can be undertaken within a co-management framework to bolster the resilience of reef-dependent communities in the face of shifting conditions. Moreover, it emphasises that in data-scarce regions, local ecological knowledge and participatory research can facilitate capacity building and generate evidence to inform locally relevant marine management and governance decisions

    Functional network changes and cognitive control in schizophrenia

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    Cognitive control is a cognitive and neural mechanism that contributes to managing the complex demands of day-to-day life. Studies have suggested that functional impairments in cognitive control associated brain circuitry contribute to a broad range of higher cognitive deficits in schizophrenia. To examine this issue, we assessed functional connectivity networks in healthy adults and individuals with schizophrenia performing tasks from two distinct cognitive domains that varied in demands for cognitive control, the RiSE episodic memory task and DPX goal maintenance task. We characterized general and cognitive control-specific effects of schizophrenia on functional connectivity within an expanded frontal parietal network (FPN) and quantified network topology properties using graph analysis. Using the network based statistic (NBS), we observed greater network functional connectivity in cognitive control demanding conditions during both tasks in both groups in the FPN, and demonstrated cognitive control FPN specificity against a task independent auditory network. NBS analyses also revealed widespread connectivity deficits in schizophrenia patients across all tasks. Furthermore, quantitative changes in network topology associated with diagnostic status and task demand were observed. The present findings, in an analysis that was limited to correct trials only, ensuring that subjects are on task, provide critical insights into network connections crucial for cognitive control and the manner in which brain networks reorganize to support such control. Impairments in this mechanism are present in schizophrenia and these results highlight how cognitive control deficits contribute to the pathophysiology of this illness

    Behavioral Health Integration in Primary Care

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    Behavioral Health Integration in Primary Care Casey Zapata, Depts. of Psychology and English, Demetrius Carter, & MaryKate Crawford, and Samantha Mladen, Emily Donovan, Amber Fox, & Kristen O’Loughlin, Dept. of Psychology Graduate Students, with Dr. Bruce Rybarczyk, Dept. of Psychology Background/Aims: Due to limited access to mental health care, many patients present to primary care with mental health concerns, such as depression and anxiety. Integrated primary care (IPC), an emerging practice model that integrates behavioral health providers with medical providers in primary care, has been demonstrated to improve patient outcomes. This project aims to characterize patients being seen in safety-net IPC, both demographically and clinically. Methods: The data were collected across three safety-net clinics in the Richmond area. The sample consisted of 96 adult patients: 68 female (71%), 24 male (25%), 1 non binary (1%), and 3 not collected (3%); 54 African-American (56%), 29 White (30%), 1 Asian (1%), 1 Other (1%), and 11 not collected (12%). Measures included a patient-completed checklist of patients’ behavioral health concerns, the PHQ-9 for depression, the GAD-7 for anxiety, and clinician-completed chart review for demographic factors. Results: Of the 72 patients who completed the GAD-7, patients reported 13 (18%) severe symptoms of anxiety, 11 (15%) moderate symptoms, 15 (21%) mild symptoms, and 33 (46%) subclinical symptoms. For the 37 patients who completed the PHQ-9, patients reported 7 (19%) severe depressive symptoms, 10 (27%) moderately severe symptoms, 12 (32%) moderate symptoms, 6 (16%) mild symptoms, and 2 (5%) subclinical symptoms. The six most commonly patient-reported problems were stress (n= 73), anxiety (n= 70), depression (n= 65), sleep (n = 55), grief (n = 53), and irritability (n= 53). When asked to rank their top three concerning problems, the five concerns most commonly ranked as top problems were: : (1) anxiety (n = 29), (2) stress (n = 28), (3) depression (n = 27), (4) sleep (n=16), and (5) weight (n=15). Further, 56 (58%) participants reported both depression and anxiety as among their top three concerns. Discussion: Anxiety and depression were reported by the majority of patients, with 33% experiencing at least moderate anxiety and 78% experiencing at least moderate depression. Additionally, anxiety and depression were cited as the third most commonly reported concerns, respectively, as well as ranked within the top three most concerning problems for most participants. Stress, anxiety, depression, and sleep were included in both the most commonly reported problems and the most common top three concerns of participants, suggesting that these concerns are both pervasive and troublesome for participants. Over time, this project will prioritize increasing sample size and tracking longitudinal trends. The continued study of safety-net IPC may allow for increasing access to behavioral health, identifying common behavioral health concerns in primary care, and meeting unmet patient needs.https://scholarscompass.vcu.edu/uresposters/1340/thumbnail.jp

    Should there be a female age limit on public funding for Assisted Reproductive Technology? Differing conceptions of justice in resource allocation

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    Should there be a female age limit on public funding for assisted reproductive technology (ART)? The question bears significant economic and sociopolitical implications and has been contentious in many countries. We conceptualise the question as one of justice in resource allocation, using three much-debated substantive principles of justice—the capacity to benefit, personal responsibility, and need—to structure and then explore a complex of arguments. Capacity-to-benefit arguments are not decisive: There are no clear cost-effectiveness grounds to restrict funding to those older women who still bear some capacity to benefit from ART. Personal responsibility arguments are challenged by structural determinants of delayed motherhood. Nor are need arguments decisive: They can speak either for or against a female age limit, depending on the conception of need used. We demonstrate how these principles can differ not only in content but also in the relative importance they are accorded by governments. Wide variation in ART public funding policy might be better understood in this light. We conclude with some inter-country comparison. New Zealand and Swedish policies are uncommonly transparent and thus demonstrate particularly well how the arguments we explore have been put into practice

    MORe PREcISE: a multicentre prospective study of patient reported outcome measures in stroke morbidity: a cross sectional study

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    Background and Purpose The use of patient reported outcomes measures (PROMs) may offer utility that are important for stroke survivors. This study assessed the PROMIS-10, which contains Mental health (MH) and Physical Health (PH) domains, with an additional five stroke specific questions. The aim of this study was to evaluate the association between the MH and PH measures following a stroke and pre-existing health conditions. Methods A multicentre prospective cohort study at 19 hospital sites across England and Wales during 2019 was conducted. The association between each PROMIS-10 domain and demographic and health conditions were calculated using a multilevel multivariable linear and present the adjusted mean difference (aMD). Results The study enrolled 549 stroke survivors within 14 days of the index event, 232 were women (42.3%) and with a mean age of 72.7 years (SD = 12.9, range 25 to 97). The MH domain was scored as poor in 3.9% of participants, and very good or excellent in almost a half (48.4%). In contrast the PH domain was scored as poor in 39.9%, compared to very good or excellent in 8.5%. The MH domain was associated with pre-existing diabetes (aMD = − 2.01; 95%CI -3.91, − 0.12; p = 0.04), previous stroke (aMD = − 3.62; 95%CI -5.86, − 1.39; p = 0.001), age (aMD = 0.07; 95%CI: 0.01, 0.14; p = 0.037), and female sex (aMD = 1.91; 95%CI 0.28, 3.54; p = 0.022). The PH domain was found to be associated with sex (female) (aMD = 2.09; 95%CI 0.54, 3.65; p = 0.008) and previous stroke (aMD = − 3.05; 95%CI -5.17, − 0.93; p = 0.005). Conclusions Almost half of stroke survivors reported poor PH using a PROM with less reporting poor MH. age, and sex were associated with both MH and PH domains, and additionally pre-exising diabetes and stroke were associated with poorer MH. Clinical management offers an opportunity to investigate and intervene to prevent long term poorer health in stroke survivors

    Parents’/caregivers’ fears and concerns about their child’s epilepsy: A scoping review

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    Background: Childhood epilepsy is a serious and common neurological condition and can have life-long consequences and its impact can pervade all aspects of family life. Whilst the medical management of seizures is important, much of the day-to-day home management of epilepsy is invisible to people external to the family, including health care professionals, and parents’/caregivers’ fears and concerns can go unacknowledged and unaddressed by health care professionals. Objective: This objective of this review was to examine parents’/caregivers’ fears and concerns regarding their child’s epilepsy, the impact of these fears and concerns on family life, the social and emotional well-being of parents/caregivers and any factors which mitigate these fears and concerns. Design: Scoping review using a modified version of Arksey and O’Malley’s framework. Data sources: Relevant studies were identified using key search terms in Scopus, Medline, CINAHL and PsychInfo databases in March 2021 with hand checking of reference lists. Search terms were developed using population (parents/caregivers of children aged ≤ 18 years with epilepsy, families); concept (parents’/caregivers’ fears, concerns, anxiety about their child’s epilepsy); and context (any setting). A further search was run in April 2022. Other inclusion criteria: English language empirical studies, 2010–2021. Study appraisal methods: A minimum of two reviewers independently screened articles and undertook data extraction and decisions were consensually made. Methodological quality appraisal was undertaken using the Mixed Methods Appraisal Tool v2018. A data extraction table was created to chart all studies. The conduct and reporting of this study followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidance for Systematic reviews and Meta-Analyses extension for Scoping Reviews (PRISMA-ScR) (S1 Table). There is no published copy of the review protocol. Main findings: The search identified a total of 4077 papers (after duplicates were removed) of which 110 were assessed for eligibility. Twenty-four papers published between 2010–2021 were included in the review and each paper was treated as a separate study. The review findings indicate that parents’/caregivers’ fears and concerns stem from more than their child’s seizures and relate to many wider aspects of family life. These fears and concerns had far-reaching influences on their parenting/caregiving, and on the lifestyle and activities of their child and their family. What was less evident was what parents/caregivers wanted in terms of support or how they thought health professionals could acknowledge and/or allay their fears and concerns. The discussion is framed within the compassion-focused therapy model as a basis for generating new thinking about the impact of these fears and concerns and the need for a new agenda for clinical consultations in childhood epilepsy. Conclusions: The review concludes with a proposal that a more compassionate agenda underpins the dialogue between parents/caregivers and clinicians to encompass and mitigate the wider emotional, psychosocial, and societal threats that impact on the parent/caregivers of children with epilepsy

    Valley View Farm: Main House

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    Prepared by the Fall 2011 Conservation of Historic Building Materials class. This historic structure report provided an assessment of present conditions, historic context, and recommendations for on going preservation of the main house located at Valley View Farm in Cartersville, Georgia. The purpose of this HSR is to provide the owners of the main house with a holistic examination of the structure and integrity of the house. Recommendations made are based on the Secretary of Interior’s Standards for Treatment of Historic Properties to maximize optimal long term preservation of this National Register property.https://scholarworks.gsu.edu/history_heritagepreservation/1041/thumbnail.jp

    Hands Up, Now What?: Black Families’ Reactions to Racial Socialization Interventions

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    Given the heightened national attention to negative race-related issues and the subsequent community solution-oriented outcry (e.g., Black Lives Matter movement), it is crucial to address healing from racial discrimination for Black Americans. Clinical and community psychologists have responded by developing and implementing programs that focus on racial socialization and psychological wellness, particularly given disproportionate issues with utilization, access, and the provision of quality services within urban and predominantly Black communities. The aim of this article is to describe 2 applied programs (Engaging, Managing, and Bonding through Race and Family Learning Villages), which seek to address and heal racial stress through crucial proximal systems—families and schools—and to highlight participant reactions. These programs offer solutions through strengths-based and participatory approaches which draw from Black Americans’ own protective mechanisms related to improved mental health. We conclude with a discussion on practice, assessments, and models specific to racial stress for researchers, practitioners, and consumers of mental health services
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