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Volumn 45, Issue 1, 2007, Pages 100-103

Do characteristics of HIPAA consent forms affect the response rate?

Author keywords

Consent forms; Health protected information; HIPAA; Response rate

Indexed keywords

ADULT; AGED; ARTICLE; FEMALE; HEALTH INSURANCE; HUMAN; INFORMATION PROCESSING; INFORMED CONSENT; LEGAL ASPECT; MALE; MIDDLE AGED; STATISTICAL MODEL; STATISTICS; UNITED STATES;

EID: 33847158024     PISSN: 00257079     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.mlr.0000241062.79855.35     Document Type: Review
Times cited : (10)

References (10)
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  • 2
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  • 3
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    • Potential impact of the HIPPA privacy rule on data collection in a registry of patients with acute coronary syndrome
    • Armstrong D, Kline-Rogers E, Jani SM, et al. Potential impact of the HIPPA privacy rule on data collection in a registry of patients with acute coronary syndrome. Arch Intern Med. 2005;165:1125-1129.
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    • Armstrong, D.1    Kline-Rogers, E.2    Jani, S.M.3
  • 4
    • 0017953420 scopus 로고
    • Informed consent: Consequences for response rate and response quality in social surveys
    • Singer E. Informed consent: consequences for response rate and response quality in social surveys. Am Sociol Rev. 1978;43:144-162.
    • (1978) Am Sociol Rev , vol.43 , pp. 144-162
    • Singer, E.1
  • 5
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    • Confidentiality assurances and response: A quantitative review of the experimental literature
    • Singer E, Von Thurn DR, Miller ER. Confidentiality assurances and response: a quantitative review of the experimental literature. Public Opin Q. 1995;59:66-77.
    • (1995) Public Opin Q , vol.59 , pp. 66-77
    • Singer, E.1    Von Thurn, D.R.2    Miller, E.R.3
  • 6
    • 0036549591 scopus 로고    scopus 로고
    • Do patient consent procedures affect participation rates in health services research?
    • Nelson K, Garcia E, et al. Do patient consent procedures affect participation rates in health services research? Med Care. 2002;40:283-288.
    • (2002) Med Care , vol.40 , pp. 283-288
    • Nelson, K.1    Garcia, E.2
  • 7
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    • Results of the National Initiative for Cancer Care Quality: How can we improve the quality of cancer care in the United States
    • Malin JL, Schneider EC, Epstein AM, et al. Results of the National Initiative for Cancer Care Quality: how can we improve the quality of cancer care in the United States. J Clin Oncol. 2006;24:626-634.
    • (2006) J Clin Oncol , vol.24 , pp. 626-634
    • Malin, J.L.1    Schneider, E.C.2    Epstein, A.M.3
  • 8
    • 4644281540 scopus 로고    scopus 로고
    • Interventions to improve research participants' understanding in informed consent for research
    • Flory J, Emanuel E. Interventions to improve research participants' understanding in informed consent for research. JAMA. 2004;292:1593-1601.
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  • 9
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    • Selection bias from requiring patients to give consent to examine data for health services research
    • Woolf SH, Rothemich SF, Johnson RE, et al. Selection bias from requiring patients to give consent to examine data for health services research. Arch Fam Med. 2000;9:1111-1118.
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    • Woolf, S.H.1    Rothemich, S.F.2    Johnson, R.E.3
  • 10
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    • Development and testing of informed consent questions to link survey data with administrative records
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.