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The burden in family caregivers of people living with dementia: prevalence and predictors.

Ma'en AljezawiRaid KofahiAbdallah Abu KhaitAsem AbdalrahimOmar Al OmariAbdullah AlkhawaldehMohammed ALBashtawyMohammad SulimanImad Abu KhaderMohammed JalladJamal A S QaddumiZaid ALBashtawySalam Bani Hani
Published in: Psychogeriatrics : the official journal of the Japanese Psychogeriatric Society (2024)
Caregivers in the current study reported no burden to a minimum burden. This result does not mean that these caregivers have no or minimal stress or that they do not have psychological needs; on the contrary, these results call for more attention to providing extra psychological and emotional support to caregivers of patients with dementia in order to decrease the burden level and maintain their efforts in caregiving. Future studies are required to discern the shape and context of unmet caregiver needs, assessment, and support.
Keyphrases
  • palliative care
  • risk factors
  • mild cognitive impairment
  • cognitive impairment
  • current status
  • sleep quality
  • quality improvement
  • depressive symptoms
  • stress induced