Behavioural interventions for enhancing life participation in behavioural variant frontotemporal dementia and primary progressive aphasia

Kathleen B. Kortte, Emily J. Rogalski

Research output: Contribution to journalArticlepeer-review

41 Scopus citations

Abstract

Primary progressive aphasia (PPA) and behavioural-variant frontotemporal dementia (bvFTD) are clinical syndromes under the umbrella term 'frontotemporal dementia' (FTD) and are caused by a neurodegenerative disease with an onset most typically in the productive years of adulthood. The cognitive and behavioural impairments associated with FTD interfere with successful engagement in typical life roles, such as parenting, working, and maintenance of interpersonal relationships. There are currently no treatments to stop or slow the degenerative process and there are only very limited medication options for the management of the cognitive-behavioural symptoms. However, alternative, non-pharmacological interventions may offer significant benefit to the quality of life of the diagnosed individual. The goal of this paper is to provide an overview of the approaches available through neurorehabilitation and community-based services that facilitate successful engagement in life activities and promote optimal quality of life for the individuals and families living with FTD. It is hoped that as medical providers become more familiar with behavioural interventions, referrals for services will increase thereby allowing individuals with FTD and their caregivers to learn ways to adapt, adjust, and participate in life to the fullest despite the impairments from this progressive disease.

Original languageEnglish (US)
Pages (from-to)237-245
Number of pages9
JournalInternational Review of Psychiatry
Volume25
Issue number2
DOIs
StatePublished - Apr 2013
Externally publishedYes

ASJC Scopus subject areas

  • Psychiatry and Mental health

Fingerprint

Dive into the research topics of 'Behavioural interventions for enhancing life participation in behavioural variant frontotemporal dementia and primary progressive aphasia'. Together they form a unique fingerprint.

Cite this