Routines of organization of clinical tests and interviews in the ELSA-Brasil investigation center

被引：134

作者：

Bensenor, Isabela M. ^{[1
]}

Griep, Rosane H. ^{[2
]}

Pinto, Karina Araujo ^{[3
]}

de Faria, Carolina Perim ^{[4
]}

Felisbino-Mendes, Mariana ^{[5
]}

Caetano, Edna I. ^{[1
]}

Albuquerque, Liliane da Silva ^{[6
]}

Schmidt, Maria Ines ^{[7
]}

机构：

[1] Univ Sao Paulo, Univ Hosp, Ctr Pesquisa Clin & Epidemiol, Sao Paulo, Brazil

[2] Fundacao Oswaldo Cruz, Inst Oswaldo Cruz, Lab Educ Ambiente & Saude, Rio De Janeiro, RJ, Brazil

[3] Univ Fed Bahia, Escola Enfermagem, Dept Enfermagem Comunitaria, Salvador, BA, Brazil

[4] Univ Fed Espirito Santo, Ctr Biomed, Vitoria, ES, Brazil

[5] Univ Fed Minas Gerais, Escola Enfermagem, Dept Enfermagem Mat Infantil & Saude Publ, Belo Horizonte, MG, Brazil

[6] Fundacao Oswaldo Cruz, Escola Nacl Saude Publ, Programa Epidemiol Saude Publ, Rio De Janeiro, RJ, Brazil

[7] Univ Fed Rio Grande do Sul, Fac Med, Programa Posgrad Epidemiol, Porto Alegre, RS, Brazil

来源：

REVISTA DE SAUDE PUBLICA | 2013年 / 47卷

关键词：

Cohort Studies; Data Collection; methods; Adult; Patient Selection; Medical History Taking; Diagnostic Techniques and Procedures; Interviews as Topic; utilization; MIDDLE-AGED ADULTS; ATHEROSCLEROSIS RISK; POSTPRANDIAL HYPERGLYCEMIA; DISEASE;

D O I：

10.1590/S0034-8910.2013047003780

中图分类号：

R1 [预防医学、卫生学];

学科分类号：

1004 ; 120402 ;

摘要：

The ELSA-Brasil (Estudo Longitudinal de Sa de do Adulto - Brazilian Longitudinal Study for Adult Health) is a prospective cohort study with extensive assessments throughout time. This article describes the routine of clinical tests and interviews performed with participants and the structuring of the Research Center physical space and teams. The ELSA-Brasil assumes that participants will be present at the Research Center to have the tests and interviews performed, according to standard protocols developed by this study. Considering the multiplicity of activities involved, each with specific needs for standardization, several predetermined orders of clinical tests and interviews were created. This ensured a high standard of quality in data collection without harm to participants' comfort. Each participant was previously assigned to a specific sequence of clinical tests and interviews with a predefined arrival time, mean length of stay of five to six hours and departure time.

引用

页码：37 / 47

页数：11

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