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Evaluation of a psychoeducational intervention compared with education in people with Parkinson's disease and their informal caregivers: a quasi-experimental study.
Navarta-Sánchez, María Victoria; Ambrosio, Leire; Portillo, Mari Carmen; Ursúa, Maria Eugenia; Senosiain, Juana M; Riverol, Mario.
Afiliação
  • Navarta-Sánchez MV; Department of Nursing, Faculty of Medicine, Autonomous University of Madrid, Madrid, Spain.
  • Ambrosio L; Faculty of Nursing, University of Navarre, Pamplona, Navarre, Spain.
  • Portillo MC; Faculty of Health Sciences, University of Southampton, Southampton, Hampshire, UK.
  • Ursúa ME; Primary Health Care Center of San Juan, Navarre Health Service, Pamplona, Navarre, Spain.
  • Senosiain JM; Faculty of Nursing, University of Navarre, Pamplona, Navarre, Spain.
  • Riverol M; Department of Neurology, University of Navarra Clinic, Pamplona, Navarre, Spain.
J Adv Nurs ; 76(10): 2719-2732, 2020 Oct.
Article em En | MEDLINE | ID: mdl-32798329
AIM: To evaluate the effects of a psychoeducational intervention compared with an education programme to strengthen quality of life, psychosocial adjustment, and coping in people with Parkinson's disease and their informal caregivers. DESIGN: A quasi-experimental study was performed with repeated measures at baseline, after the intervention and 6 months post-intervention. METHODS: The study was carried out at seven primary care centres from 2015-2017. A total of 140 people with Parkinson's and 127 informal caregivers were allocated to the experimental and the control groups. The experimental group received a 9-week psychoeducational intervention, whereas the control group received a 5-week education programme. Repeated measures ANOVA were used to test differences in quality of life, psychosocial adjustment, and coping between the experimental and control groups and over time. RESULTS: Patients and informal caregivers in both the experimental and control groups showed significantly better psychosocial adjustment at the post-intervention measurement compared with baseline data. We also found significantly greater quality of life in patients and coping skills in caregivers after the end of the interventions in the experimental and control groups. Nevertheless, no significant differences were identified on the outcomes at the 6-month post-intervention measurement. CONCLUSION: The effect of the psychoeducational intervention was not different from the effect of the education programme. The strategies applied in both interventions followed a group approach led by a multidisciplinary team covering information about PD, healthy lifestyles, and social resources. They might be easily sustained in Primary Care to improve care for people with Parkinson's and informal caregivers.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson Idioma: En Ano de publicação: 2020 Tipo de documento: Article