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Problem-focused coping underlying lower caregiver burden in ALS-FTD: implications for caregiver intervention
Jashelle Caga1,2, Margaret C Zoing1, David Foxe1,3
1Brain & Mind Centre, The University of Sydney, Camperdown, Australia.
Caregiver support for amyotrophic lateral sclerosis (ALS) patients, especially those with ALS-frontotemporal dementia (ALS-FTD), should focus on problem-solving coping strategies to reduce caregiver burden. This approach is more effective than addressing anxiety, depression, or stress alone.
Area of Science:
- Neuroscience
- Psychology
- Gerontology
Background:
- Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease impacting multiple systems, often presenting with cognitive and behavioral symptoms similar to frontotemporal dementia (FTD).
- Caregiver support is crucial for managing these cognitive and behavioral symptoms in ALS, yet research in this area remains limited.
- Understanding caregiver coping mechanisms is vital for developing effective interventions within ALS care.
Purpose of the Study:
- To investigate the associations between caregiver coping strategies, psychological distress, and the burden experienced by caregivers of individuals with ALS.
- To specifically examine these relationships within the context of ALS patients exhibiting cognitive and behavioral symptoms characteristic of FTD.
- To identify key factors that predict caregiver burden in ALS patient-caregiver dyads.
Main Methods:
- Fifty-five patient-caregiver dyads were recruited from specialized ALS and FTD clinics.
- Coping strategies were assessed using the COPE Inventory/Brief COPE.
- Psychological morbidity and burden were measured using the Depression, Anxiety, and Stress Scale-21 and Zarit Burden Interview, with data analyzed using univariate and multivariate statistics.
Main Results:
- Caregivers of patients diagnosed with ALS-FTD reported significantly higher burden (p=.0001).
- Problem-focused coping strategies, particularly planning, were utilized more frequently than emotion-focused or dysfunctional strategies.
- ALS-FTD diagnosis (p=.0001) and the use of problem-focused coping strategies (p=.024) were significant predictors of caregiver burden, whereas anxiety, depression, and stress were not (p=.151).
Conclusions:
- Multidisciplinary ALS care should incorporate timely caregiver support that emphasizes problem-focused coping strategies.
- This approach is particularly important for caregivers of patients with ALS-FTD to help mitigate their burden.
- Interventions should aim to enhance problem-focused coping to effectively manage the challenges associated with caring for individuals with ALS.
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