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Volumn 24, Issue SUPPL. 1, 2010, Pages

A Collaborative Alzheimer disease research exchange: Using a community-based helpline as a recruitment tool

Author keywords

Alzheimer disease research; recruitment and retention issues

Indexed keywords

ALZHEIMER DISEASE; ARTICLE; CAREGIVER; CLINICAL RESEARCH; COOPERATION; HUMAN; PARTICIPATORY RESEARCH; PATIENT PARTICIPATION; PRIORITY JOURNAL; TELEPHONE; UNITED STATES;

EID: 77956442528     PISSN: 08930341     EISSN: None     Source Type: Journal    
DOI: 10.1097/WAD.0b013e3181f11f8d     Document Type: Article
Times cited : (9)

References (14)
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  • 2
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  • 4
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    • Barriers to obtaining consent in dementia research: Implications for surrogate decision-making
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  • 5
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  • 6
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    • Lingler JH, Parker LS, DeKosky ST, et al. Caregivers as subjects of clinical drug trials: a review of human subjects protection practices in published studies of Alzheimer disease pharmacotherapies. IRB Ethics Hum Res. 2006;28: 11-18.
    • (2006) IRB Ethics Hum Res , vol.28 , pp. 11-18
    • Lingler, J.H.1    Parker, L.S.2    Dekosky, S.T.3
  • 7
    • 60549105569 scopus 로고    scopus 로고
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    • Kim SYH, Kim HM, Langa KM, et al. Surrogate consent for dementia research: a national survey of older Americans. Neurology. 2009;72:149-155.
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  • 8
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    • Caregivers attitudes toward their family members participation in Alzheimer disease research: Implications for recruitment and retention
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    • Connell, C.M.1    Shaw, B.A.2    Holmes, S.B.3
  • 9
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    • July 11-16 Vienna, Austria
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  • 10
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.