SAGE Journals Online
Advertisement
Sign In to gain access to subscriptions and/or personal tools.

 

Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Advertisement

Sign In to gain access to subscriptions and/or personal tools.
American Journal of Alzheimer's Disease and Other Dementias®
This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Ready, R. E.
Right arrow Articles by Grace, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ready, R. E.
Right arrow Articles by Grace, J.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Insight and Cognitive Impairment

Effects on Quality-of-Life Reports From Mild Cognitive Impairment and Alzheimer's Disease Patients

Rebecca E. Ready

University of Massachusetts, Department of Psychology, 135 Hicks Way, Tobin Hall 609, Amherst, MA 01003; ready{at}psych.umass.edu

Brian R. Ott

Janet Grace

This study follows previous work to determine the effect of patient insight and cognitive impairment on the reliability and validity of self-reported quality of life (QOL) from patients diagnosed with Alzheimer's disease (AD) and mild cognitive impairment (MCI). AD and MCI patients (N = 68) and their caregivers participated. Patients with impaired insight provided QOL ratings that were less reliable than those provided by patients with better insight. Patient-caregiver agreement for QOL reports was used as an index of validity. Neither better insight nor lesser cognitive impairment suggested better agreement. Thus, even when patient insight is intact, patient reports are unlikely to agree with caregiver reports. Patient and caregiver reports about patient QOL may represent 2 unique, yet potentially valid, perspectives.

Key Words: mild cognitive impairment • Alzheimer's disease • quality of life • caregiver • insight • reliability • validity • self-report

American Journal of Alzheimer's Disease and Other Dementias®, Vol. 21, No. 4, 242-248 (2006)
DOI: 10.1177/1533317506290589


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
AM J ALZHEIMERS DIS OTHER DEMENHome page
E. Londos, K. Boschian, A. Linden, C. Persson, L. Minthon, and J. Lexell
Effects of a Goal-Oriented Rehabilitation Program in Mild Cognitive Impairment: A Pilot Study
American Journal of Alzheimer's Disease and Other Dementias, May 1, 2008; 23(2): 177 - 183.
[Abstract] [PDF]


Home page
AM J ALZHEIMERS DIS OTHER DEMENHome page
R. E. Ready and B. R. Ott
Integrating Patient and Informant Reports on the Cornell-Brown Quality-of-Life Scale
American Journal of Alzheimer's Disease and Other Dementias, January 1, 2008; 22(6): 528 - 534.
[Abstract] [PDF]



Advertisement