The Impact of HIPAA Authorization on Willingness to Participate in Clinical Research

Annals of Epidemiology

Volumn 17, Issue 11, 2007, Pages 899-905

  Dunlop, Anne L ^a   Graham, Tracie ^a   Leroy, Zanie ^a   Glanz, Karen ^b   Dunlop, Boadie ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b EMORY UNIVERSITY   (United States)

Author keywords

Clinical Trial; Consent Forms; Health Insurance Portability and Accountability Act; Minority Groups; Patient Participation

Indexed keywords

ANTIHYPERTENSIVE AGENT;

ADULT; AFRICAN AMERICAN; ARTICLE; ATTITUDE TO HEALTH; CLINICAL RESEARCH; COMPREHENSION; CONTROLLED STUDY; FEAR; FEMALE; HEALTH INSURANCE; HUMAN; INFORMED CONSENT; LAW; MAJOR CLINICAL STUDY; MALE; PATIENT DECISION MAKING; PATIENT PARTICIPATION; PRIORITY JOURNAL; PRIVACY; REFUSAL TO PARTICIPATE; RESEARCH SUBJECT;

ADULT; AFRICAN AMERICANS; CLINICAL TRIALS AS TOPIC; CROSS-SECTIONAL STUDIES; EDUCATIONAL STATUS; FEMALE; HEALTH INSURANCE PORTABILITY AND ACCOUNTABILITY ACT; HUMANS; INFORMED CONSENT; MALE; PATIENT PARTICIPATION; RESEARCH SUBJECTS; UNITED STATES;

EID: 35348874824     PISSN: 10472797     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.annepidem.2007.05.006     Document Type: Article

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