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Factors associated with symptoms of depression among informal caregivers of people with systemic sclerosis: a cross-sectional study

Scleroderma Caregiver Advisory Com, Canedo-Ayala, M., Rice, D. B., Levis, B., Carrier, M-E., Cumin, J., Malcarne, V. L., Hagedoorn, M. & Thombs, B. D., 30-Jan-2020, In : Disability and Rehabilitation. 42, 3, p. 394-399 6 p.

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  • Factors associated with symptoms of depression among informal caregivers of people with systemic sclerosis

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DOI

  • Scleroderma Caregiver Advisory Com
  • Mara Canedo-Ayala
  • Danielle B. Rice
  • Brooke Levis
  • Marie-Eve Carrier
  • Julie Cumin
  • Vanessa L. Malcarne
  • Mariet Hagedoorn
  • Brett D. Thombs

Purpose: Our study aimed to identify caregiver characteristics (gender, age, occupational status, educational attainment, relation to care recipient), care recipient characteristics (age, disease subtype), and caregiving factors (hours of care, perceived caregiving burden) associated with symptoms of depression among informal caregivers of persons with systemic sclerosis (also known scleroderma). as Materials and methods: A questionnaire was developed and administered online from December 2016 to June 2017 to informal caregivers of people with scleroderma, including the Patient Health Questionnaire-9 to assess depressive symptoms. Multiple linear regression was used to identify factors associated with depressive symptoms. Results: Caregivers (n = 202) were 60.9% male. Average age was 57.2 years (standard deviation = 14.4 years). Most caregivers were partners (72.3%), children (11.9%), or parents (7.4%), of care recipients. Self-reported caregiving burden (standardized regression coefficient = 0.54, p <0.001) and hours of care per week ( = 0.17, p = 0.005) were significantly associated with greater symptoms of depression. Conclusions: Depressive symptoms were primarily associated with caregiving burden among a sample of scleroderma caregivers. There is need to develop interventions targeting caregivers in scleroderma. Rehabilitation professionals should consider the specific needs of scleroderma caregivers and should provide or refer to support services as appropriate.

Original languageEnglish
Pages (from-to)394-399
Number of pages6
JournalDisability and Rehabilitation
Volume42
Issue number3
Publication statusPublished - 30-Jan-2020

    Keywords

  • Caregivers, rare disease, depressive symptoms, scleroderma, systemic sclerosis, PSYCHOLOGICAL HEALTH, DISEASE, BURDEN, COMMUNITY, CARE, DEMENTIA, INTERVENTIONS, PREVALENCE, PREDICTORS, SUPPORT

ID: 132704110