Using patient and proxy reports as outcome measures in Alzheimer disease research

Alzheimer Disease and Associated Disorders

Volumn 11, Issue SUPPL. 6, 1997, Pages 179-180

  Burgio, Louis ^a   Leon, Joel ^b  

^a UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^b Health Affairs   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALZHEIMER DISEASE; CAREGIVER; CONFERENCE PAPER; INFORMATION; OUTCOMES RESEARCH; PRIORITY JOURNAL; SOCIAL PSYCHOLOGY; WORKSHOP;

ALZHEIMER DISEASE; CAREGIVERS; COGNITION DISORDERS; DATA COLLECTION; HUMANS; INTERVIEWS; OUTCOME ASSESSMENT (HEALTH CARE); QUALITY OF LIFE; REPRODUCIBILITY OF RESULTS; SELF ASSESSMENT (PSYCHOLOGY);

EID: 0031458473     PISSN: 08930341     EISSN: None     Source Type: Journal    
DOI: 10.1097/00002093-199709000-00012     Document Type: Conference Paper

References (3)

1. Kane RL. Which outcomes matter in Alzheimer disease and who should define them? Alzheimer Dis Assoc Disord 1997;11(Suppl 6):12-7.
2. Magaziner J. Use of proxies to measure health and functional outcomes in effectiveness research in persons with Alzheimer disease and related disorders. Alzheimer Dis Assoc Disord 1997;11(Suppl 6):168-74.
3. Whitehouse P, Maslow K. Defining and measuring outcomes in Alzheimer disease: introduction and overview. Alzheimer Dis Assoc Disord 1997;11(Suppl 6):1-6.