𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Evaluating a model of caregiving for people with psychosis

✍ Scribed by J. Joyce; M. Leese; E. Kuipers; G. Szmukler; T. Harris; E. Staples


Publisher
Springer-Verlag
Year
2003
Tongue
English
Weight
253 KB
Volume
38
Category
Article
ISSN
1433-9285

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Intervening to reduce distress in caregi
✍ David J. Harper; Paul R. Manasse; Owen James; J. Tim Newton 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 567 KB

Data from a sample of 82 impaired elderly people and their carers were gathered before (Tl) they started to receive support from a home-based care aide service. Several variables were significantly correlated with, but only two were predictive of reported carer distress at T1. Data gathered from a s

Quasi-experimental evaluation of an educ
✍ Professor Henry Brodaty; Kate Roberts; Karin Peters 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 891 KB

Dementia caregivers are known to be distressed and may be helped by psychoeducational interventions. We investigated the effectiveness of one model of intervention comprising a structured package of six sessions of training, focusing on education, stress management and problem behaviour management i

The nature of informal caregiving for me
✍ Jane McCusker; Eric Latimer; Martin Cole; Antonio Ciampi; Maida Sewitch 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 83 KB 👁 1 views

## Abstract ## Objectives To describe patient and caregiver perceptions of the nature of informal caregiving in a sample of older medical inpatients with and without depression. ## Methods One hundred and fifty‐four patient‐caregiver pairs were recruited from a larger prospective observational s

Development of an educational programme
✍ Marcia Finlayson; Jennifer Dahl Garcia; Katharine Preissner 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 151 KB

## Abstract This article describes a three‐phase project to identify and develop an occupational therapy response to the challenges experienced by caregivers of middle‐aged and older adults with multiple sclerosis (MS). In Phase 1 302 caregivers of middle‐aged and older adults with MS were intervie