Problem-Focused Coping Underlying Lower Caregiver Burden in ALS-FTD: Implications for Caregiver Intervention

Caga, Jashelle, Zoing, Margaret, Foxe, David, Ramsey, Eleanor, D’Mello, Mirelle, Mioshi, Eneida, Ahmed, Rebekah M., Kiernan, Matthew C. and Piguet, Olivier (2020) Problem-Focused Coping Underlying Lower Caregiver Burden in ALS-FTD: Implications for Caregiver Intervention. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. ISSN 2167-8421 (In Press)

[img] PDF (Accepted_Manuscript) - Submitted Version
Restricted to Repository staff only until 31 December 2099.

Download (308kB) | Request a copy

Abstract

Objective: Amyotrophic lateral sclerosis (ALS) is a multisystem neurodegenerative disorder which includes cognitive and behavioural symptoms akin to frontotemporal dementia (FTD). Despite the necessity of caregiver intervention to assist with the management of cognitive and behavioural symptoms, there has been a lack of research on the topic. A focus on caregiver coping may offer a promising foundation to guide the development of interventions as part of ALS care. Accordingly, the aim of the present study was to examine the relationships between caregiver coping, psychological morbidity and burden of care in the context of ALS cognitive and behavioural symptoms. Methods: Fifty-five patient-caregiver dyads were recruited from specialised ALS and FTD clinics. Specific coping strategies were examined using the COPE Inventory/Brief COPE and psychological morbidity and burden were assessed using the Depression, Anxiety, and Stress Scale–21 and Zarit Burden Interview. The relationship between coping, psychological morbidity and burden of care were analysed using univariate and multivariate methods. Results: High-burden caregivers were more likely to be caring for patients with a diagnosis of ALS-FTD (p =.0001). Caregivers used problem-focused strategies (particularly planning) more frequently (M=71.4, SD=15.3) compared to emotion-focused (M=60.8, SD=12.3) and dysfunctional coping strategies (M=42.2, SD=8.6). A diagnosis of ALS-FTD (p=.0001) and problem-focused strategies (p=.024) emerged as significant predictors of caregiver burden. Caregiver anxiety, depression and stress were not predictive of caregiver burden (p=.151). Conclusions: Timely provision of caregiver support optimising problem-focused coping strategies as part of multidisciplinary ALS care, particularly for caregivers of ALS-FTD patients may mitigate caregiver burden.

Item Type: Article
Faculty \ School: Faculty of Medicine and Health Sciences > School of Health Sciences
Depositing User: LivePure Connector
Date Deposited: 11 Dec 2020 00:49
Last Modified: 11 Dec 2020 00:49
URI: https://ueaeprints.uea.ac.uk/id/eprint/77958
DOI:

Actions (login required)

View Item View Item