When others decide: Reasons for allowing patients with Alzheimer's disease to participate in nontherapeutic research

International Psychogeriatrics

Volumn 10, Issue 4, 1998, Pages 435-436

  Lynöe, Niels ^a   Sandlund, Mikael ^a   Jacobsson, Lars ^a  

^a UMEÅ UNIVERSITY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ALZHEIMER DISEASE; ARTICLE; CLINICAL RESEARCH; DECISION MAKING; FAMILY; HUMAN; INFORMED CONSENT; NORMAL HUMAN;

BIOMEDICAL AND BEHAVIORAL RESEARCH; EMPIRICAL APPROACH;

AGED; ALZHEIMER DISEASE; DECISION MAKING; FAMILY; HUMAN EXPERIMENTATION; HUMANS; MOTIVATION; THIRD-PARTY CONSENT;

EID: 0032445423     PISSN: 10416102     EISSN: None     Source Type: Journal    
DOI: 10.1017/S104161029800550X     Document Type: Article

References (1)

1. Lynöe, N., Sandlund, M., Dahlqvist, G., & Jacobsson, L. (1991). Informed consent: Study of the quality of information given to participants in a clinical trial. British Medical Journal 303, 610-613.