Literature DB >> 19674927

The benefits of a standardized patient education program for patients with Parkinson's disease and their caregivers.

L E I A'Campo1, E M Wekking, N G A Spliethoff-Kamminga, S Le Cessie, R A C Roos.   

Abstract

The Patient Education Program Parkinson (PEPP) is a standardized psychosocial intervention aiming at improving the health-related quality of life (Hr-Qol) of patients with Parkinson's disease (PD) and caregivers. A randomized controlled trial was performed to assess its effectiveness. Sixty-four PD patients and 46 caregivers were allocated to either the intervention group (PEPP) or the control group (usual care). The intervention consisted of eight weekly sessions of 90-minute duration. Assessments were performed on psychosocial problems (BELA-P/A-k), Hr-Qol (PDQ-39/EQ-5D) and depression (SDS) at baseline and one week after the end of the PEPP. Participants rated their mood on a visual analogue scale before and after each session. A significant effect for the caregivers on psychosocial problems and need for help was found and a trend for significance for patients' quality of life. Patients' and caregivers' mood improved significantly after each session. This study provides indications that PD patients and caregivers benefit from the PEPP. Copyright 2009 Elsevier Ltd. All rights reserved.

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Year:  2009        PMID: 19674927     DOI: 10.1016/j.parkreldis.2009.07.009

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN: 1353-8020            Impact factor:   4.891


  25 in total

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Authors:  Cornelie D Andela; Nicolasine D Niemeijer; Margreet Scharloo; Jitske Tiemensma; Shaaji Kanagasabapathy; Alberto M Pereira; Noëlle G A Kamminga; Ad A Kaptein; Nienke R Biermasz
Journal:  Pituitary       Date:  2015-02       Impact factor: 4.107

2.  Self-management program participation and social support in Parkinson's disease: Mixed methods evaluation.

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3.  Effects of Non-Pharmacological Treatments on Quality of Life in Parkinson's Disease: A Review.

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4.  The relationship between Parkinson's disease symptoms and caregiver quality of life.

Authors:  Richard S Henry; Sarah K Lageman; Paul B Perrin
Journal:  Rehabil Psychol       Date:  2020-02-17

Review 5.  Current Knowledge on the Evolution of Care Partner Burden, Needs, and Coping in Parkinson's Disease.

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6.  Health-related quality of life and strain in caregivers of Australians with Parkinson's disease: an observational study.

Authors:  David H Kelly; Jennifer L McGinley; Frances E Huxham; Hylton B Menz; Jennifer J Watts; Robert Iansek; Anna T Murphy; Mary Danoudis; Brooke Adair; Meg E Morris
Journal:  BMC Neurol       Date:  2012-07-17       Impact factor: 2.474

7.  Quality of life in Parkinson's disease caregivers: the contribution of personality traits.

Authors:  Eloise H Tew; Sharon L Naismith; Marilia Pereira; Simon J G Lewis
Journal:  Biomed Res Int       Date:  2013-08-19       Impact factor: 3.411

8.  The role of cognitive-behavioural therapy for patients with depression in Parkinson's disease.

Authors:  Andreas Charidimou; John Seamons; Caroline Selai; Anette Schrag
Journal:  Parkinsons Dis       Date:  2011-06-08

9.  Educational Needs and Considerations for a Visual Educational Tool to Discuss Parkinson's Disease.

Authors:  Sean J Udow; Douglas E Hobson; Galit Kleiner; Mario Masellis; Susan H Fox; Anthony E Lang; Connie Marras
Journal:  Mov Disord Clin Pract       Date:  2017-11-27

10.  A Patient-Based Needs Assessment for Living Well with Parkinson Disease: Implementation via Nominal Group Technique.

Authors:  Galit Kleiner-Fisman; Pearl Gryfe; Gary Naglie
Journal:  Parkinsons Dis       Date:  2013-02-17
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