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A changing and aging population contributes to an increase of Alzheimer-type or related dementia. Encouraged by health policies, home care for patients suffering from these conditions is often dependent on their caregivers' contribution. The demands of such a role may weaken the caregivers and cause them a feeling of burden requiring the recourse to periods of respite. An ancillary study of a research program carried out in the Geneva agglomeration, our study aims to characterize, for the caregivers of patients with dementia, the determinants of a recourse to the devices of respite.

Déterminants du recours au répit pour les proches aidants de malades atteints de démence