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| dc.contributor.author | Martín‐Carrasco, Manuel | |
| dc.contributor.author | Valero, Carmelo Pelegrín | |
| dc.contributor.author | Millán, Pedro Roy | |
| dc.contributor.author | García, Celso Iglesias | |
| dc.contributor.author | Montalbán, Salvador Ros | |
| dc.contributor.author | Vázquez, Ana Luisa Gobartt | |
| dc.contributor.author | Piris, Sonia Pons | |
| dc.contributor.author | Vilanova, Montserrat Balañá | |
| dc.contributor.author | Franco Martín, Manuel Ángel | |
| dc.date.accessioned | 2024-02-08T09:39:31Z | |
| dc.date.available | 2024-02-08T09:39:31Z | |
| dc.date.issued | 2008 | |
| dc.identifier.issn | 0885-6230 | |
| dc.identifier.uri | http://hdl.handle.net/10366/155531 | |
| dc.description.abstract | [EN] Objectives Caregivers of patients with Alzheimer’s disease (AD) experience physical and psychological stress due to the caring experience. This study evaluated the benefits of a Psychoeducational Intervention Program (PIP) on caregiver burden in southern Europe. Methods A multicentre, prospective, randomised study was conducted. One hundred and fifteen caregivers of patients with clinical diagnosis of AD (DSM-IV-TR criteria, mini-mental score¼10–26) and functional impairment (Lawton and Brody Scale and Katz Index) were recruited. Caregivers were randomised to receive either PIP (IG: intervention group, n¼60) or standard care (CG: control group, n¼55). PIP consisted of eight individual sessions over 4 months for teaching strategies for confronting problems of AD patient care. Caregivers’ stress, quality of life and perceived health were measured using validated scales (Zarit, SF-36, GHQ-28, respectively) at baseline and after 4 and 10-months follow-up. Results Mean change in caregiver burden (Zarit baseline–Zarit final scores) was statistically significant (p¼0.0083) showing an improvement in the IG ( 8.09 points) and a worsening in the CG (2.08 points). The IG showed significant improvements in all the well-being perception areas measured by the SF-36 and a significantly lower score in the GHQ-28 (p¼0.0004). 97.7% of caregivers and 88.6% of therapists considered PIP ‘useful/very useful’ at 4 months (the end of PIP) whereas at 10 months the estimates were 93.2% and 86.3%, respectively. Conclusions Psychosocial training of caregivers can minimise caregiver distress and help them to develop problemsolving strategies. A PIP improves quality of life and the perceived health of caregivers of patients with AD. | es_ES |
| dc.language.iso | eng | es_ES |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 Internacional | * |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
| dc.subject | Caregiver | es_ES |
| dc.subject | Burden | es_ES |
| dc.subject | Alzheimer’s disease | es_ES |
| dc.subject | Psychoeducational program | es_ES |
| dc.subject | Southern Europe | es_ES |
| dc.subject | Dementia | es_ES |
| dc.title | Effectiveness of a psychoeducational intervention program in the reduction of caregiver burden in alzheimer's disease patients' caregivers | es_ES |
| dc.type | info:eu-repo/semantics/article | es_ES |
| dc.identifier.doi | 10.1002/gps.2142 | |
| dc.rights.accessRights | info:eu-repo/semantics/openAccess | es_ES |
| dc.identifier.essn | 1099-1166 | |
| dc.journal.title | International Journal of Geriatric Psychiatry | es_ES |
| dc.volume.number | 24 | es_ES |
| dc.issue.number | 5 | es_ES |
| dc.page.initial | 489 | es_ES |
| dc.page.final | 499 | es_ES |
| dc.type.hasVersion | info:eu-repo/semantics/publishedVersion | es_ES |








