Literature DB >> 23212677

Enhancing quality of life and mastery of informal caregivers of high-grade glioma patients: a randomized controlled trial.

Florien W Boele1, Wopke Hoeben, Karen Hilverda, Jeroen Lenting, Anne-Lucia Calis, Eefje M Sizoo, Emma H Collette, Jan J Heimans, Martin J B Taphoorn, Jaap C Reijneveld, Martin Klein.   

Abstract

High-grade gliomas (HGG) are serious primary brain tumors that may prevent the patient from functioning normally in social, emotional and cognitive respect. Often the partner's role will convert to that of informal caregiver. Consequently, they may experience significant stress and reductions in caregiver mastery, negatively affecting their health-related quality of life (HRQOL). We aimed at (1) determining factors that impact HRQOL and mastery of caregivers of HGG patients, and (2) investigate if a structured intervention consisting of psychoeducation and cognitive behavioral therapy leads to improvements in the mental component of HRQOL and mastery of caregivers. Fifty-six patient-caregiver dyads were randomly assigned to the intervention group or the care as usual group. The intervention program consisted of six one-hour sessions with a psychologist. Participants completed questionnaires concerning their perceptions of the patients' HRQOL (SF-36), neurological functioning (BN20), and cognitive functioning (MOS), and concerning their own HRQOL (SF-36) and feelings of caregiver mastery (CMS) both at baseline (i.e. before randomization) and every 2 months thereafter until 8 months later, five times in total. Patients' HRQOL and neurological functioning were found to be related to HRQOL and feelings of mastery of the informal caregiver at baseline. The intervention helped caregivers in maintaining a stable level of HRQOL and improved feelings of mastery over an 8 month period. Our findings suggest that informal caregivers can benefit from a psychological intervention as it is a helpful tool in maintaining a stable level of mental functioning and caregiver mastery.

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Year:  2012        PMID: 23212677     DOI: 10.1007/s11060-012-1012-3

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  36 in total

Review 1.  Psychosocial and neuropsychiatric aspects of patients with primary brain tumors.

Authors:  M A Weitzner
Journal:  Cancer Invest       Date:  1999       Impact factor: 2.176

Review 2.  Family and caregiver needs over the course of the cancer trajectory.

Authors:  Barbara A Given; Charles W Given; Paula R Sherwood
Journal:  J Support Oncol       Date:  2012-01-04

3.  The development and psychometric validation of a brain cancer quality-of-life questionnaire for use in combination with general cancer-specific questionnaires.

Authors:  D Osoba; N K Aaronson; M Muller; K Sneeuw; M A Hsu; W K Yung; M Brada; E Newlands
Journal:  Qual Life Res       Date:  1996-02       Impact factor: 4.147

Review 4.  How can informal caregivers in cancer and palliative care be supported? An updated systematic literature review of interventions and their effectiveness.

Authors:  Richard Harding; Sally List; Eleni Epiphaniou; Hannah Jones
Journal:  Palliat Med       Date:  2011-07-07       Impact factor: 4.762

5.  A psycho-educational intervention for family caregivers of patients receiving palliative care: a randomized controlled trial.

Authors:  Peter L Hudson; Sanchia Aranda; Karla Hayman-White
Journal:  J Pain Symptom Manage       Date:  2005-10       Impact factor: 3.612

6.  The structure of coping.

Authors:  L I Pearlin; C Schooler
Journal:  J Health Soc Behav       Date:  1978-03

7.  Reducing emotional distress in people caring for patients receiving specialist palliative care. Randomised trial.

Authors:  Kiri Walsh; Louise Jones; Adrian Tookman; Christina Mason; Joanne McLoughlin; Robert Blizard; Michael King
Journal:  Br J Psychiatry       Date:  2007-02       Impact factor: 9.319

8.  Caring for someone with high-grade glioma: a time of rapid change for caregivers.

Authors:  Ruth McConigley; Georgia Halkett; Elizabeth Lobb; Anna Nowak
Journal:  Palliat Med       Date:  2010-02-01       Impact factor: 4.762

9.  End-of-life care and the effects of bereavement on family caregivers of persons with dementia.

Authors:  Richard Schulz; Aaron B Mendelsohn; William E Haley; Diane Mahoney; Rebecca S Allen; Song Zhang; Larry Thompson; Steven H Belle
Journal:  N Engl J Med       Date:  2003-11-13       Impact factor: 91.245

10.  Improving depression and enhancing resilience in family dementia caregivers: a pilot randomized placebo-controlled trial of escitalopram.

Authors:  Helen Lavretsky; Prabha Siddarth; Michael R Irwin
Journal:  Am J Geriatr Psychiatry       Date:  2010-02       Impact factor: 4.105

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  39 in total

Review 1.  Neuro-oncology family caregiving: review and directions for future research.

Authors:  Paula R Sherwood; Maureen Cwiklik; Heidi S Donovan
Journal:  CNS Oncol       Date:  2015-12-17

2.  Interventions to help support caregivers of people with a brain or spinal cord tumour.

Authors:  Florien W Boele; Alasdair G Rooney; Helen Bulbeck; Paula Sherwood
Journal:  Cochrane Database Syst Rev       Date:  2019-07-02

3.  Feasibility Testing and Refinement of a Supportive Educational Intervention for Carers of Patients with High-Grade Glioma - a Pilot Study.

Authors:  Georgia K B Halkett; Elizabeth A Lobb; Lisa Miller; Thérèse Shaw; Rachael Moorin; Anne Long; Anne King; Jenny Clarke; Stephanie Fewster; Anna K Nowak
Journal:  J Cancer Educ       Date:  2018-10       Impact factor: 2.037

4.  Concordance of patient and caregiver reports in evaluating quality of life in patients with malignant gliomas and an assessment of caregiver burden.

Authors:  Daniel I Jacobs; Priya Kumthekar; Becky V Stell; Sean A Grimm; Alfred W Rademaker; Laurie Rice; James P Chandler; Kenji Muro; MaryAnne Marymont; Irene B Helenowski; Lynne I Wagner; Jeffrey J Raizer
Journal:  Neurooncol Pract       Date:  2014-05-05

5.  Do carer's levels of unmet needs change over time when caring for patients diagnosed with high-grade glioma and how are these needs correlated with distress?

Authors:  G K B Halkett; E A Lobb; T Shaw; M M Sinclair; L Miller; E Hovey; A K Nowak
Journal:  Support Care Cancer       Date:  2017-08-14       Impact factor: 3.603

6.  Exploring the cancer caregiver's journey through web-based Meaning-Centered Psychotherapy.

Authors:  A J Applebaum; K L Buda; E Schofield; M Farberov; N D Teitelbaum; K Evans; R Cowens-Alvarado; R S Cannady
Journal:  Psychooncology       Date:  2017-12-19       Impact factor: 3.894

7.  Survivorship care planning and implementation in neuro-oncology.

Authors:  Heather Leeper; Kathrin Milbury
Journal:  Neuro Oncol       Date:  2018-11-09       Impact factor: 12.300

8.  Interaction of quality of life, mood and depression of patients and their informal caregivers after surgical treatment of high-grade glioma: a prospective study.

Authors:  Maxi Sacher; Jürgen Meixensberger; Wolfgang Krupp
Journal:  J Neurooncol       Date:  2018-08-02       Impact factor: 4.130

9.  Predicting distress among people who care for patients living longer with high-grade malignant glioma.

Authors:  B Russell; A Collins; A Dowling; M Dally; M Gold; M Murphy; J Burchell; J Philip
Journal:  Support Care Cancer       Date:  2015-04-25       Impact factor: 3.603

10.  The multidimensional burden of informal caregivers in primary malignant brain tumor.

Authors:  Eléonore Bayen; Florence Laigle-Donadey; Myrtille Prouté; Khê Hoang-Xuan; Marie-Eve Joël; Jean-Yves Delattre
Journal:  Support Care Cancer       Date:  2016-09-13       Impact factor: 3.603

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