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      Assessing the Validity of Self-rated Health Across Ethnic Groups: Implications for Health Disparities Research

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          Self-Rated Health and Mortality: A Review of Twenty-Seven Community Studies

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            Social conditions as fundamental causes of health inequalities: theory, evidence, and policy implications.

            Link and Phelan (1995) developed the theory of fundamental causes to explain why the association between socioeconomic status (SES) and mortality has persisted despite radical changes in the diseases and risk factors that are presumed to explain it. They proposed that the enduring association results because SES embodies an array of resources, such as money, knowledge, prestige, power, and beneficial social connections that protect health no matter what mechanisms are relevant at any given time. In this article, we explicate the theory, review key findings, discuss refinements and limits to the theory, and discuss implications for health policies that might reduce health inequalities. We advocate policies that encourage medical and other health-promoting advances while at the same time breaking or weakening the link between these advances and socioeconomic resources. This can be accomplished either by reducing disparities in socioeconomic resources themselves or by developing interventions that, by their nature, are more equally distributed across SES groups.
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              The National Survey of American Life: a study of racial, ethnic and cultural influences on mental disorders and mental health

              The objectives of the National Survey of American Life (NSAL) are to investigate the nature, severity, and impairment of mental disorders among national samples of the black and non‐Hispanic white (n = 1,006) populations in the US. Special emphasis in the study is given to the nature of race and ethnicity within the black population by selecting and interviewing national samples of African‐American (N = 3,570), and Afro‐Caribbean (N = 1,623) immigrant and second and older generation populations. National multi‐stage probability methods were used in generating the samples and race/ethnic matching of interviewers and respondents were used in the largely face‐to‐face interview, which lasted on average 2 hours and 20 minutes. The Diagnostic and Statistical Manual (DSM) IV World Mental Health Composite Interview (WHO‐CIDI) was used to assess a wide range of serious mental disorders, potential risk and resilience factors, and help seeking and service use patterns. This paper provides an overview of the design of the NSAL, sample selection procedures, recruitment and training of the national interviewing team, and some of the special problems faced in interviewing ethnically and racially diverse national samples. Unique features of sample design, including special screening and listing procedures, interviewer training and supervision, and response rate outcomes are described. Copyright © 2004 Whurr Publishers Ltd.
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                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                Journal of Racial and Ethnic Health Disparities
                J. Racial and Ethnic Health Disparities
                Springer Science and Business Media LLC
                2197-3792
                2196-8837
                February 05 2021
                Article
                10.1007/s40615-021-00977-x
                33544329
                45ee6c42-2729-4a70-8bf8-1c83d1b267ad
                © 2021

                http://www.springer.com/tdm

                http://www.springer.com/tdm

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