Literature DB >> 35796675

"Living Well" Trajectories Among Family Caregivers of People With Mild-to-Moderate Dementia in the IDEAL Cohort.

Linda Clare1,2, Laura D Gamble3, Anthony Martyr1, Serena Sabatini1, Sharon M Nelis1, Catherine Quinn4,5, Claire Pentecost1, Christina Victor6, Roy W Jones7, Ian R Jones8, Martin Knapp9, Rachael Litherland10, Robin G Morris11, Jennifer M Rusted12, Jeanette M Thom13, Rachel Collins1, Catherine Henderson9, Fiona E Matthews3.   

Abstract

OBJECTIVES: Understanding whether and how caregivers' capability to "live well" changes over time, and the factors associated with change, could help target effective caregiver support.
METHODS: We analyzed 3 time points (12 months apart) of Improving the experience of Dementia and Enhancing Active Life (IDEAL) cohort data from coresident spouse caregivers of community-dwelling individuals who had mild-to-moderate dementia at baseline, using latent growth and growth mixture models. Capability to "live well" was derived from measures of quality of life, well-being, and satisfaction with life.
RESULTS: Data from 995 spouse caregivers at Time 1, 780 at Time 2, and 601 at Time 3 were included. The mean "living well" score decreased slightly over time. We identified 3 classes of caregivers: one with higher baseline scores declining slightly over time (Stable; 66.8%), one with low baseline scores remaining stable (Lower Stable; 26.0%), and one with higher baseline scores showing marked decline (Declining; 7.2%). Scores on baseline measures differentiated the Lower Stable, but not the Declining, from the Stable class. Longitudinally, the Declining class was associated with care recipient cognitive decline and increasing hours providing care, as well as caregiver stress and depression. Findings were similar when caregivers with other kin relationships were included. DISCUSSION: The findings indicate the importance of prompt identification of, and support for, caregivers at risk of the declining capability to "live well" and may assist in identifying those caregivers who could benefit most from targeted support.
© The Author(s) 2022. Published by Oxford University Press on behalf of The Gerontological Society of America.

Entities:  

Keywords:  Alzheimer’s; Longitudinal; Quality of life; Satisfaction with life; Well-being

Mesh:

Year:  2022        PMID: 35796675      PMCID: PMC9535787          DOI: 10.1093/geronb/gbac090

Source DB:  PubMed          Journal:  J Gerontol B Psychol Sci Soc Sci        ISSN: 1079-5014            Impact factor:   4.942


  39 in total

1.  Caregiving and the stress process: an overview of concepts and their measures.

Authors:  L I Pearlin; J T Mullan; S J Semple; M M Skaff
Journal:  Gerontologist       Date:  1990-10

2.  Just one question: If one question works, why ask several?

Authors:  Ann Bowling
Journal:  J Epidemiol Community Health       Date:  2005-05       Impact factor: 3.710

3.  Negative impact and positive value in caregiving: validation of the COPE index in a six-country sample of carers.

Authors:  Cristian Balducci; Eva Mnich; Kevin J McKee; Giovanni Lamura; Anke Beckmann; Barbro Krevers; Z Beata Wojszel; Mike Nolan; Constantinos Prouskas; Barbara Bien; Birgitta Oberg
Journal:  Gerontologist       Date:  2008-06

4.  Changes in the balance between formal and informal care supply in England between 2001 and 2011: evidence from census data.

Authors:  Valentina Zigante; Jose-Luis Fernandez; Fernanda Mazzotta
Journal:  Health Econ Policy Law       Date:  2020-07-02

5.  Distinguishing optimism from neuroticism (and trait anxiety, self-mastery, and self-esteem): a reevaluation of the Life Orientation Test.

Authors:  M F Scheier; C S Carver; M W Bridges
Journal:  J Pers Soc Psychol       Date:  1994-12

6.  Caregivers' relationship closeness with the person with dementia predicts both positive and negative outcomes for caregivers' physical health and psychological well-being.

Authors:  Elizabeth Fauth; Kyle Hess; Kathy Piercy; Maria Norton; Chris Corcoran; Peter Rabins; Constantine Lyketsos; JoAnn Tschanz
Journal:  Aging Ment Health       Date:  2012       Impact factor: 3.658

7.  Influence of Positive and Negative Dimensions of Dementia Caregiving on Caregiver Well-Being and Satisfaction With Life: Findings From the IDEAL Study.

Authors:  Catherine Quinn; Sharon M Nelis; Anthony Martyr; Christina Victor; Robin G Morris; Linda Clare
Journal:  Am J Geriatr Psychiatry       Date:  2019-02-11       Impact factor: 4.105

8.  A Comprehensive Model of Factors Associated With Capability to "Live Well" for Family Caregivers of People Living With Mild-to-Moderate Dementia: Findings From the IDEAL Study.

Authors:  Linda Clare; Yu-Tzu Wu; Catherine Quinn; Ian R Jones; Christina R Victor; Sharon M Nelis; Anthony Martyr; Rachael Litherland; James A Pickett; John V Hindle; Roy W Jones; Martin Knapp; Michael D Kopelman; Robin G Morris; Jennifer M Rusted; Jeanette M Thom; Ruth A Lamont; Catherine Henderson; Isla Rippon; Alexandra Hillman; Fiona E Matthews
Journal:  Alzheimer Dis Assoc Disord       Date:  2019 Jan-Mar       Impact factor: 2.703

9.  Predictors of the one-year-change in depressiveness in informal caregivers of community-dwelling people with dementia.

Authors:  Lara Kürten; Nikolas Dietzel; Peter L Kolominsky-Rabas; Elmar Graessel
Journal:  BMC Psychiatry       Date:  2021-04-03       Impact factor: 3.630

10.  Determinants of overburdening among informal carers: a systematic review.

Authors:  Nienke Lindt; Jantien van Berkel; Bob C Mulder
Journal:  BMC Geriatr       Date:  2020-08-26       Impact factor: 3.921

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