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本文引用的文献

1
Sibling perspectives on severe mental illness: reflections on self and family.兄弟姐妹对严重精神疾病的看法:对自我和家庭的反思
Am J Orthopsychiatry. 2004 Oct;74(4):489-501. doi: 10.1037/0002-9432.74.4.489.
2
The Tuskegee Study of Untreated Syphilis and public perceptions of biomedical research: a focus group study.塔斯基吉未治疗梅毒研究与公众对生物医学研究的认知:一项焦点小组研究
J Natl Med Assoc. 2004 Aug;96(8):1051-64.
3
Public beliefs about schizophrenia and depression: similarities and differences.公众对精神分裂症和抑郁症的看法:异同点。
Soc Psychiatry Psychiatr Epidemiol. 2003 Sep;38(9):526-34. doi: 10.1007/s00127-003-0676-6.
4
Distrust, race, and research.不信任、种族与研究。
Arch Intern Med. 2002 Nov 25;162(21):2458-63. doi: 10.1001/archinte.162.21.2458.
5
Increasing participation of minorities in cancer clinical trials: summary of the "Moving Beyond the Barriers" Conference in North Carolina.少数族裔在癌症临床试验中参与度的提高:北卡罗来纳州“突破障碍”会议总结
J Natl Med Assoc. 2002 Jan;94(1):31-9.
6
African Americans' views on research and the Tuskegee Syphilis Study.非裔美国人对研究及塔斯基吉梅毒研究的看法。
Soc Sci Med. 2001 Mar;52(5):797-808. doi: 10.1016/s0277-9536(00)00178-7.
7
Knowledge of the Tuskegee study and its impact on the willingness to participate in medical research studies.对塔斯基吉研究及其对参与医学研究意愿的影响的了解。
J Natl Med Assoc. 2000 Dec;92(12):563-72.
8
Factors that influence African-Americans' willingness to participate in medical research studies.影响非裔美国人参与医学研究意愿的因素。
Cancer. 2001 Jan 1;91(1 Suppl):233-6. doi: 10.1002/1097-0142(20010101)91:1+<233::aid-cncr10>3.0.co;2-8.
9
Dispelling the stigma of schizophrenia: II. The impact of information on dangerousness.消除精神分裂症的污名:二、信息对危险性的影响。
Schizophr Bull. 1999;25(3):437-46. doi: 10.1093/oxfordjournals.schbul.a033391.
10
Public conceptions of mental illness: labels, causes, dangerousness, and social distance.公众对精神疾病的认知:标签、成因、危险性及社会距离。
Am J Public Health. 1999 Sep;89(9):1328-33. doi: 10.2105/ajph.89.9.1328.

非裔美国人社区对精神分裂症及医学研究的态度与认知:一项探索性研究。

African-American community attitudes and perceptions toward schizophrenia and medical research: an exploratory study.

作者信息

Hamilton Lynnae A, Aliyu Muktar H, Lyons Paul D, May Roberta, Swanson Charlie L, Savage Robert, Go Rodney C P

机构信息

Fielding Graduate University, Santa Barbara, CA, USA.

出版信息

J Natl Med Assoc. 2006 Jan;98(1):18-27.

PMID:16532974
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2594797/
Abstract

INTRODUCTION

Ensuring adequate representation of all demographic groups in medical research is necessary in order to ensure that the benefits associated with participation are equitably shared. Mental health research is unique in that the stigma associated with mental illness, such as schizophrenia, further hinders participation. Using focus groups, we set out to explore the attitudes and views of African Americans with regard to schizophrenia and medical research.

METHODS

Four focus group discussions were conducted, with 23 participants divided into two groups of working and retired adults, and two groups of full- and part-time students selected from inner-city residents of Birmingham, AL, and surrounding counties. Data obtained were analyzed using the content analysis method.

RESULTS

Diverse views were expressed about the cause of mental illness, and much of this was influenced by cultural beliefs. There was considerable misunderstanding of schizophrenia, and the majority of participants described the disease in terms of positive symptoms only. Whereas for older participants the Tuskegee syphilis study experience was an important factor in their reluctance to participate in medical research, younger participants expressed no knowledge of the study. Among younger participants an assumed level of social distrust was evident, with prominent fear of participating in research that employs physically intrusive methods.

CONCLUSION

The provision of accurate information through trusted community sources and open dialogue will help to dispel myths, correct faulty assumptions and increase African-American participation in schizophrenia research.

摘要

引言

为确保参与医学研究的益处能公平分配,必须保证医学研究能充分代表所有人口群体。心理健康研究具有独特性,因为与精神疾病(如精神分裂症)相关的污名进一步阻碍了人们的参与。我们通过焦点小组来探究非裔美国人对精神分裂症和医学研究的态度与看法。

方法

进行了四次焦点小组讨论,23名参与者分为两组,一组是在职和退休成年人,另一组是从阿拉巴马州伯明翰市及周边县的市中心居民中选取的全日制和非全日制学生。使用内容分析法对获得的数据进行分析。

结果

参与者对精神疾病的病因表达了多种观点,其中很多受到文化信仰的影响。对精神分裂症存在相当多的误解,大多数参与者仅从阳性症状方面描述该疾病。对于年长参与者而言,塔斯基吉梅毒研究经历是他们不愿参与医学研究的一个重要因素,而年轻参与者表示对该研究一无所知。在年轻参与者中,明显存在一种假定的社会不信任,他们极度害怕参与采用身体侵入性方法的研究。

结论

通过可靠的社区渠道提供准确信息并开展开放对话,将有助于消除误解、纠正错误假设,并提高非裔美国人参与精神分裂症研究的比例。