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2.
Arch Womens Ment Health ; 21(2): 203-214, 2018 04.
Artigo em Inglês | MEDLINE | ID: mdl-28956168

RESUMO

Poor postnatal mental health is a major public health issue, and risk factors include experiencing adverse life events during pregnancy. We assessed whether midwifery group practice, compared to standard hospital care, would protect women from the negative impact of a sudden-onset flood on postnatal depression and anxiety. Women either received midwifery group practice care in pregnancy, in which they were allocated a primary midwife who provided continuity of care, or they received standard hospital care provided by various on-call and rostered medical staff. Women were pregnant when a sudden-onset flood severely affected Queensland, Australia, in January 2011. Women completed questionnaires on their flood-related hardship (objective stress), emotional reactions (subjective stress), and cognitive appraisal of the impact of the flood. Self-report assessments of the women's depression and anxiety were obtained during pregnancy, at 6 weeks and 6 months postnatally. Controlling for all main effects, regression analyses at 6 weeks postpartum showed a significant interaction between maternity care type and objective flood-related hardship and subjective stress, such that depression scores increased with increasing objective and subjective stress with standard care, but not with midwifery group practice (continuity), indicating a buffering effect of continuity of midwifery carer. Similar results were found for anxiety scores at 6 weeks, but only with subjective stress. The benefits of midwifery continuity of carer in pregnancy extend beyond a more positive birth experience and better birthing and infant outcomes, to mitigating the effects of high levels of stress experienced by women in the context of a natural disaster on postnatal mental health.


Assuntos
Desastres , Inundações , Tocologia , Estresse Psicológico/prevenção & controle , Adulto , Depressão Pós-Parto/epidemiologia , Depressão Pós-Parto/etiologia , Depressão Pós-Parto/prevenção & controle , Feminino , Humanos , Estudos Longitudinais , Masculino , Pessoa de Meia-Idade , Gravidez , Queensland/epidemiologia , Fatores de Risco , Apoio Social , Fatores Socioeconômicos , Estresse Psicológico/epidemiologia , Estresse Psicológico/etiologia , Adulto Jovem
3.
BMJ Open ; 6(8): e010916, 2016 08 18.
Artigo em Inglês | MEDLINE | ID: mdl-27540096

RESUMO

OBJECTIVES: (1) To test the use of best-worst scaling (BWS) experiments in valuing different types of biomedical and health research impact, and (2) to explore how different types of research impact are valued by different stakeholder groups. DESIGN: Survey-based BWS experiment and discrete choice modelling. SETTING: The UK. PARTICIPANTS: Current and recent UK Medical Research Council grant holders and a representative sample of the general public recruited from an online panel. RESULTS: In relation to the study's 2 objectives: (1) we demonstrate the application of BWS methodology in the quantitative assessment and valuation of research impact. (2) The general public and researchers provided similar valuations for research impacts such as improved life expectancy, job creation and reduced health costs, but there was less agreement between the groups on other impacts, including commercial capacity development, training and dissemination. CONCLUSIONS: This is the second time that a discrete choice experiment has been used to assess how the general public and researchers value different types of research impact, and the first time that BWS has been used to elicit these choices. While the 2 groups value different research impacts in different ways, we note that where they agree, this is generally about matters that are seemingly more important and associated with wider social benefit, rather than impacts occurring within the research system. These findings are a first step in exploring how the beneficiaries and producers of research value different kinds of impact, an important consideration given the growing emphasis on funding and assessing research on the basis of (potential) impact. Future research should refine and replicate both the current study and that of Miller et al in other countries and disciplines.


Assuntos
Pesquisa Biomédica/normas , Pesquisadores , Pesquisa Biomédica/economia , Pesquisa Biomédica/tendências , Comportamento de Escolha , Grupos Focais , Humanos , Avaliação de Resultados em Cuidados de Saúde , Inquéritos e Questionários , Reino Unido
4.
Schizophr Res ; 95(1-3): 86-95, 2007 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-17693059

RESUMO

OBJECTIVE: The aim of this study was to examine the reliability, validity and factor structure of the Community Assessment of Psychic Experiences (CAPE), a 42-item self-report questionnaire. We analyzed the internal consistency of the CAPE to determine whether the 3-factor structure (positive, negative and depressive symptoms) found by the CAPE authors would also be found in our sample. METHOD: A sample of 2275 individuals from the general community in the Montreal area completed the questionnaire in either French or English. RESULTS: The internal consistencies of the original three subscales were good and the confirmatory factor models had a good fit. The exploratory factor analysis suggested a 3-5-factor solution, without improving the alternative factor structures. The 4-factor solution separated positive symptoms into factors we called 'bizarre positive symptoms' and 'social delusions', and the 5-factor solution separated positive symptoms further and included a 'popular psychic beliefs' factor. Results suggest that the scalability might be improved by shortening the original questionnaire to 23 items with the same 3 original scales. CONCLUSION: We support the internal consistency of the CAPE. Although alternative scaling (4 and 5 factors) did not improve the model fit, researchers interested in distinguishing 3 factors of positive symptoms could find utility in these two new scales. Finally, reducing the number of CAPE items could be useful for shorter surveys. Future studies should test the implications of these suggestions.


Assuntos
Inventário de Personalidade/estatística & dados numéricos , Esquizofrenia/diagnóstico , Psicologia do Esquizofrênico , Adolescente , Adulto , Canadá , Coleta de Dados , Delusões/diagnóstico , Delusões/psicologia , Depressão/diagnóstico , Depressão/psicologia , Escolaridade , Análise Fatorial , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , América do Norte , Parapsicologia , Prognóstico , Psicometria , Reprodutibilidade dos Testes , Fatores de Risco , Comportamento Social , Inquéritos e Questionários , Traduções
5.
Psychiatry Res ; 117(3): 211-22, 2003 Mar 25.
Artigo em Inglês | MEDLINE | ID: mdl-12686364

RESUMO

Our objectives were to determine the extent to which symptoms in the schizophrenia patient and personality in the mother lead to a sense of subjective burden in the mother, and to explain variance in two components of Expressed Emotion. Data on symptom severity (PANSS), mothers' personality (NEO-PI), subjective burden (SBAS), and Expressed Emotion (CFI) were gathered from 41 schizophrenia outpatients and their mothers. Approximately one quarter of the variance in Critical Comments (CCs) and Emotional Overinvolvement (EOI) was explained using path analysis. Mothers' CCs were associated with more severe excitement in the patient, with lower Neuroticism, and greater burden in the mother. Higher EOI was explained by greater Conscientiousness and burden in the mother; patient depression had a weak indirect effect on maternal EOI. These results characterize the high EE mother as low in neuroticism and high in conscientiousness with a particular sensitivity to excitement and depression in the patient.


Assuntos
Afeto , Atitude Frente a Saúde , Mães/psicologia , Transtornos da Personalidade/psicologia , Esquizofrenia , Adulto , Efeitos Psicossociais da Doença , Feminino , Humanos , Masculino , Transtornos da Personalidade/diagnóstico , Transtornos da Personalidade/epidemiologia , Inventário de Personalidade , Psicologia do Esquizofrênico , Índice de Gravidade de Doença
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