Sociodemographic reporting and sample composition over 3 decades of psychopathology research: A systematic review and quantitative synthesis.

IF 3.1 Q2 PSYCHIATRY
Sylia Wilson
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Abstract

Although researchers seek to understand psychological phenomena in a population, quantitative research studies are conducted in smaller samples meant to represent the larger population of interest. This systematic review and quantitative synthesis considers reporting of sociodemographic characteristics and sample composition in the Journal of Abnormal Psychology (now the Journal of Psychopathology and Clinical Science) over the past 3 decades. Across k = 1,244 empirical studies, there were high and increasing rates of reporting of participant age/developmental stage and sex/gender, low but increasing reporting of socioeconomic status/income, and moderate and stable reporting of educational attainment. Rates of reporting of sexual orientation remained low and reporting of gender identity was essentially nonexistent. There were low to moderate but increasing rates of reporting of participant race and ethnicity. Approximately three-quarters of participants in studies over the past 3 decades were White, while the proportion of participants who were Asian, Black or African American, American Indian or Alaska Native, Native Hawaiian or Other Pacific Islander, or Hispanic/Latino was much lower. Approximately two-thirds of participants were female, with this proportion increasing over time. There were also notable differences in the proportion of study participants as a function of race and sex/gender for different forms of psychopathology. Basic science and theoretical psychopathology research must include sociodemographically diverse samples that are representative of and generalizable to the larger human population, while seeking to decrease stigma of psychopathology and increase mental health equity. Recommendations are made to increase sociodemographic diversity in psychopathology research and the scientific review/publication process. (PsycInfo Database Record (c) 2023 APA, all rights reserved).

心理病理学研究三十年来的社会人口报告和样本组成:系统回顾与定量综合。
尽管研究人员试图了解群体中的心理现象,但定量研究是在较小的样本中进行的,目的是代表更大的相关群体。这篇系统性综述和定量综述研究了过去 30 年来《变态心理学杂志》(现为《精神病理学与临床科学杂志》)中有关社会人口特征和样本组成的报道。在 k = 1,244 项实证研究中,对参与者年龄/发育阶段和性别/性取向的报告率较高且呈上升趋势,对社会经济地位/收入的报告率较低但呈上升趋势,对教育程度的报告率适中且稳定。性取向的报告率仍然较低,性别认同的报告率基本为零。对参与者种族和民族的报告率从低到中度不等,但呈上升趋势。在过去 30 年的研究中,大约四分之三的参与者是白人,而亚裔、黑人或非裔美国人、美国印第安人或阿拉斯加原住民、夏威夷原住民或其他太平洋岛民、西班牙裔/拉丁美洲人的比例要低得多。约三分之二的参与者为女性,这一比例随着时间的推移而增加。就不同形式的精神病理学而言,研究参与者的种族和性别比例也存在明显差异。基础科学和理论性精神病理学研究必须包括具有社会人口统计学意义的多样化样本,这些样本应能代表更广泛的人类群体并具有普遍性,同时寻求减少精神病理学的污名化并提高心理健康的公平性。本文提出了在精神病理学研究和科学审查/出版过程中增加社会人口多样性的建议。(PsycInfo Database Record (c) 2023 APA,保留所有权利)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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