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Williams 综合征干预研究参与者的多样性。

Diversity of Participants in Williams Syndrome Intervention Studies.

机构信息

Lurie Center for Autism, 1 Maguire Road, Lexington, MA, 02421, USA.

Haverford College, Haverford, PA, USA.

出版信息

J Autism Dev Disord. 2024 Oct;54(10):3888-3898. doi: 10.1007/s10803-023-06088-2. Epub 2023 Aug 16.

Abstract

PURPOSE

This study describes participant diversity in Williams syndrome (WS) intervention studies.

METHODS

A literature search was conducted to identify prospective treatment studies including participants with WS. Data was extracted on the reporting of and information provided on age, sex, cognitive ability, socioeconomic status, race, and ethnicity.

RESULTS

Eleven eligible articles were identified. Reporting rates of demographic factors varied considerably, with the highest rates for age and sex (100%) and the lowest reporting rates for race (18%) and ethnicity (9%). Combining demographic data from the two studies that reported on race and/or ethnicity (n = 33), 88% of participants were White. The combined participant mean age was 20.9 years.

CONCLUSION

There is a low frequency of reporting on several demographic factors including socioeconomic status, race, and ethnicity in WS intervention studies. There is a need for increased representation of racial and ethnic minority groups, older participants, and more cognitively impaired patients in WS research.

摘要

目的

本研究描述了威廉姆斯综合征(WS)干预研究中的参与者多样性。

方法

进行了文献检索,以确定包括 WS 患者在内的前瞻性治疗研究。提取了关于年龄、性别、认知能力、社会经济地位、种族和民族的报告和信息。

结果

确定了 11 篇符合条件的文章。人口统计学因素的报告率差异很大,年龄和性别(100%)的报告率最高,种族(18%)和民族(9%)的报告率最低。将报告种族和/或民族的两项研究中的人口统计学数据合并(n=33),88%的参与者为白人。合并的参与者平均年龄为 20.9 岁。

结论

WS 干预研究中,有几个人口统计学因素(包括社会经济地位、种族和民族)的报告频率较低。需要增加 WS 研究中少数族裔、年龄较大的参与者和认知障碍更严重的患者的代表性。

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