Literature DB >> 24588692

Correlates of psychological distress in study partners of older people with and without mild cognitive impairment (MCI) - the Sydney Memory and Ageing Study.

Katrin M Seeher1, Lee-Fay Low, Simone Reppermund, Melissa J Slavin, Brian M Draper, Kristan Kang, Nicole A Kochan, Julian N Trollor, Perminder S Sachdev, Henry Brodaty.   

Abstract

OBJECTIVES: Psychological effects of supporting someone with mild cognitive impairment (MCI) are often overlooked. We aimed to establish correlates of psychological distress in study partners of individuals with and without nonclinical MCI.
METHODS: Demographic, psychosocial and health measures were obtained cross-sectionally from 714 participants (39% MCI) and study partners of a longitudinal community-based study on cognitive aging. Study partners (i.e. family members/friends) were categorized as providing support with instrumental everyday activities or not. Psychological distress was measured by the Kessler psychological distress scale. Multiple hierarchical regressions examined determinants of psychological distress within Pearlin's stress process model.
RESULTS: Psychological distress was generally low and not associated with MCI or whether study partners provided support or not. Instead, distress was greater if participants were male irrespective of study partners' sex and if study partners reported negative reactions to participants' behavioral symptoms, felt burdened by providing support and showed worse coping abilities; overall explaining 37% variance. Self-rated disability and aspects of health-related quality of life explained additional 7%.
CONCLUSION: Objective impairment measures were not associated with distress in partners or supporters. However, study partners' appraisals of functional and behavioral symptoms were linked to increased distress even in this very mildly affected community cohort.

Entities:  

Keywords:  behavior; burden; caregiver; instrumental activities of daily living; prodromal dementia

Mesh:

Year:  2014        PMID: 24588692     DOI: 10.1080/13607863.2013.875123

Source DB:  PubMed          Journal:  Aging Ment Health        ISSN: 1360-7863            Impact factor:   3.658


  4 in total

1.  Impact of Alzheimer's disease on the family caregiver's long-term quality of life: results from an ALSOVA follow-up study.

Authors:  Tarja H Välimäki; Janne A Martikainen; Kristiina Hongisto; Saku Väätäinen; Harri Sintonen; Anne M Koivisto
Journal:  Qual Life Res       Date:  2015-09-09       Impact factor: 4.147

2.  Dyadic Analysis of Illness Perceptions Among Persons with Mild Cognitive Impairment and Their Family Members.

Authors:  Jennifer H Lingler; Lauren Terhorst; Richard Schulz; Amanda Gentry; Oscar Lopez
Journal:  Gerontologist       Date:  2015-04-15

3.  Sex, Neuropsychiatric Profiles, and Caregiver Burden in Alzheimer's Disease Dementia: A Latent Class Analysis.

Authors:  Maitée Rosende-Roca; Pilar Cañabate; Mariola Moreno; Silvia Preckler; Susana Seguer; Ester Esteban; Juan Pablo Tartari; Liliana Vargas; Leire Narvaiza; Vanesa Pytel; Urszula Bojaryn; Emilio Alarcon; Antonio González-Pérez; Miren Jone Gurruchaga; Lluís Tárraga; Agustín Ruiz; Marta Marquié; Mercè Boada; Sergi Valero
Journal:  J Alzheimers Dis       Date:  2022       Impact factor: 4.160

4.  Researchers' perspectives on the role of study partners in dementia research.

Authors:  Betty S Black; Holly Taylor; Peter V Rabins; Jason Karlawish
Journal:  Int Psychogeriatr       Date:  2014-07-03       Impact factor: 3.878

  4 in total

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