Evaluation of an educational program for the caregivers of persons diagnosed with a malignant glioma

Background: Caring for a loved one with a malignant glioma can be a formidable responsibility. The guarded prognosis, side effects of treatments, and changes in brain function, personality and behaviour pose unique challenges in care provision by family members. It is rare that institutions provide...

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Main Authors: Rosemary Cashman, Lori J. Bernstein, Denise Bilodeau, Geoff Bowet, Barbara Jackson, Masoud Yousefi, Anca Prica, James Perry
Format: Article
Language:English
Published: Pappin Communications 2007-01-01
Series:Canadian Oncology Nursing Journal
Online Access:http://www.canadianoncologynursingjournal.com/index.php/conj/article/view/274/277
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spelling doaj-2f8d4e0921914c75845000a63f292b872020-11-24T23:48:14ZengPappin CommunicationsCanadian Oncology Nursing Journal2368-80762007-01-0117161010.5737/1181912x171610Evaluation of an educational program for the caregivers of persons diagnosed with a malignant gliomaRosemary Cashman0Lori J. Bernstein1Denise Bilodeau2Geoff Bowet3Barbara Jackson4Masoud Yousefi5Anca Prica6James Perry7At the time of writing, Rosemary Cashman, RN, MA, MSc(A), ACNP, was an Advanced Practice Nurse, Neuro-oncology, Crolla Family Brain Tumour Research Unit, Sunnybrook Health Sciences Centre, Toronto, ON.PhD, Psychologist, Crolla Family Brain Tumour Research Unit, Sunnybrook Health Sciences Centre, Toronto, ON.BSW, MSW, RSW, Social Worker, Sunnybrook Health Sciences Centre, Toronto, ON. MD, Palliative Physician, Sunnybrook Health Sciences Centre, Toronto, ON.BScOT, OTReg(Ont), Occupational Therapist, Sunnybrook Health Sciences Centre, Toronto, ON.MSc, Statistician, Brain Research Centre, University of British Columbia, Vancouver, BC.MD, University of Toronto School of Medicine, Toronto, ON.MD, Neuro-oncologist, Crolla Family Brain Tumour Research Unit, Sunnybrook Health Sciences Centre, Toronto, ON.Background: Caring for a loved one with a malignant glioma can be a formidable responsibility. The guarded prognosis, side effects of treatments, and changes in brain function, personality and behaviour pose unique challenges in care provision by family members. It is rare that institutions provide educational programs for caregivers. Purpose: To evaluate the impact of providing information in an educational program to caregivers of patients diagnosed with a malignant glioma. Methods: A structured educational program for caregivers of brain tumour patients was developed based upon multidisciplinary expert opinion and caregiver feedback. Twenty-four caregiver participants were enrolled in the program. Knowledge was assessed before, immediately following, and four to six weeks following the program. Open-ended questions were used to explore the caregivers’ experiences, as well as additional benefits derived from the program. Results: Knowledge scores on testing immediately after the program and four to six weeks following the program were statistically significantly improved from baseline testing, although there was a decline in scores four to six weeks after the program. These findings demonstrate effective knowledge transfer (recall of the information) immediately after the education program and four to six weeks later. Specific qualitative and quantitative data serve as a basis for understanding caregivers’ needs and experiences.http://www.canadianoncologynursingjournal.com/index.php/conj/article/view/274/277
collection DOAJ
language English
format Article
sources DOAJ
author Rosemary Cashman
Lori J. Bernstein
Denise Bilodeau
Geoff Bowet
Barbara Jackson
Masoud Yousefi
Anca Prica
James Perry
spellingShingle Rosemary Cashman
Lori J. Bernstein
Denise Bilodeau
Geoff Bowet
Barbara Jackson
Masoud Yousefi
Anca Prica
James Perry
Evaluation of an educational program for the caregivers of persons diagnosed with a malignant glioma
Canadian Oncology Nursing Journal
author_facet Rosemary Cashman
Lori J. Bernstein
Denise Bilodeau
Geoff Bowet
Barbara Jackson
Masoud Yousefi
Anca Prica
James Perry
author_sort Rosemary Cashman
title Evaluation of an educational program for the caregivers of persons diagnosed with a malignant glioma
title_short Evaluation of an educational program for the caregivers of persons diagnosed with a malignant glioma
title_full Evaluation of an educational program for the caregivers of persons diagnosed with a malignant glioma
title_fullStr Evaluation of an educational program for the caregivers of persons diagnosed with a malignant glioma
title_full_unstemmed Evaluation of an educational program for the caregivers of persons diagnosed with a malignant glioma
title_sort evaluation of an educational program for the caregivers of persons diagnosed with a malignant glioma
publisher Pappin Communications
series Canadian Oncology Nursing Journal
issn 2368-8076
publishDate 2007-01-01
description Background: Caring for a loved one with a malignant glioma can be a formidable responsibility. The guarded prognosis, side effects of treatments, and changes in brain function, personality and behaviour pose unique challenges in care provision by family members. It is rare that institutions provide educational programs for caregivers. Purpose: To evaluate the impact of providing information in an educational program to caregivers of patients diagnosed with a malignant glioma. Methods: A structured educational program for caregivers of brain tumour patients was developed based upon multidisciplinary expert opinion and caregiver feedback. Twenty-four caregiver participants were enrolled in the program. Knowledge was assessed before, immediately following, and four to six weeks following the program. Open-ended questions were used to explore the caregivers’ experiences, as well as additional benefits derived from the program. Results: Knowledge scores on testing immediately after the program and four to six weeks following the program were statistically significantly improved from baseline testing, although there was a decline in scores four to six weeks after the program. These findings demonstrate effective knowledge transfer (recall of the information) immediately after the education program and four to six weeks later. Specific qualitative and quantitative data serve as a basis for understanding caregivers’ needs and experiences.
url http://www.canadianoncologynursingjournal.com/index.php/conj/article/view/274/277
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