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Research Article

Religiousness is positively associated with quality of life of ALS caregivers

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Pages 168-171 | Received 27 Nov 2010, Accepted 02 Feb 2011, Published online: 25 Feb 2011

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Raquel Gehrke Panzini, Bruno Paz Mosqueiro, Rogério R. Zimpel, Denise Ruschel Bandeira, Neusa S. Rocha & Marcelo P. Fleck. (2017) Quality-of-life and spirituality. International Review of Psychiatry 29:3, pages 263-282.
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Kristen Qutub, David Lacomis, Stephen M. Albert & Eleanor Feingold. (2014) Life factors affecting depression and burden in amyotrophic lateral sclerosis caregivers. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 15:3-4, pages 292-297.
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Articles from other publishers (21)

Bethany Faith Leidl, Debbi Fox-Davis, Francis O. Walker, Jennifer Gabbard & Buddy Marterre. (2023) Layers of Loss: A Scoping Review and Taxonomy of HD Caregivers’ Spiritual Suffering, Grief/Loss and Coping Strategies. Journal of Pain and Symptom Management 65:1, pages e29-e50.
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In Seo La, Meg Johantgen, Carla L. Storr, John G. Cagle, Shijun Zhu & Alyson Ross. (2020) Spirituality among family caregivers of cancer patients: The Spiritual Perspective Scale. Research in Nursing & Health 43:4, pages 407-418.
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Klaudia Kukulka, Karla T. Washington, Raghav Govindarajan & David R. Mehr. (2019) Stakeholder Perspectives on the Biopsychosocial and Spiritual Realities of Living With ALS: Implications for Palliative Care Teams. American Journal of Hospice and Palliative Medicine® 36:10, pages 851-857.
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Victor Counted, Adam Possamai & Tanya Meade. (2018) Relational spirituality and quality of life 2007 to 2017: an integrative research review. Health and Quality of Life Outcomes 16:1.
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Morten Magelssen, Trygve Holmøy, Morten Andreas Horn, Ove Arne Fondenæs, Knut Dybwik & Reidun Førde. (2018) Ethical challenges in tracheostomy-assisted ventilation in amyotrophic lateral sclerosis. Journal of Neurology 265:11, pages 2730-2736.
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Augusta Silveira, Sara Amaral, Ana Rosa Castro, Eurico Monteiro, Francisco Pimentel & Teresa Sequeira. (2018) Cancer Palliative Care: Technology Support for Quality of Life Assessment of Family Caregivers. Procedia Computer Science 138, pages 294-302.
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Cathy Gluyas, Susan Mathers, Nicole Hennessy Anderson & Anna Ugalde. (2016) Factors to consider for motor neurone disease carer intervention research: A narrative literature review. Palliative and Supportive Care 15:5, pages 600-608.
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Stephanie Johnson, Bryant Alonso, Katie Faulkner, Haley Roberts, Britton Monroe, Leigh Lehman & Pamalyn Kearney. (2017) Quality of Life Perspectives of People With Amyotrophic Lateral Sclerosis and Their Caregivers. The American Journal of Occupational Therapy 71:3, pages 7103190010p1-7103190010p7.
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Susan Bergin & Carole Mockford. (2016) Recommendations to support informal carers of people living with motor neurone disease. British Journal of Community Nursing 21:10, pages 518-524.
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Mary R. O'brien & David Clark. (2015) Spirituality and/or religious faith: A means for coping with the effects of amyotrophic lateral sclerosis/motor neuron disease?. Palliative and Supportive Care 13:6, pages 1603-1614.
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Fabia B Weisser, Katherine Bristowe & Diana Jackson. (2015) Experiences of burden, needs, rewards and resilience in family caregivers of people living with Motor Neurone Disease/Amyotrophic Lateral Sclerosis: A secondary thematic analysis of qualitative interviews. Palliative Medicine 29:8, pages 737-745.
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Sabrina Paganoni, Chafic Karam, Nanette Joyce, Richard Bedlack & Gregory T. Carter. (2015) Comprehensive rehabilitative care across the spectrum of amyotrophic lateral sclerosis. NeuroRehabilitation 37:1, pages 53-68.
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Gabriela Romano de Oliveira, José Fittipaldi Neto, Sthephanie Marques de Camargo, Alessandra Lamas Granero Lucchetti, Daniele Corcioli Mendes Espinha & Giancarlo Lucchetti. (2015) Caregiving across the lifespan: comparing caregiver burden, mental health, and quality of life. Psychogeriatrics 15:2, pages 123-132.
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Dezhi Chen, Xiaoyan Guo, Zhenzhen Zheng, Qianqian Wei, Wei Song, Bei Cao, Rui Huang, Rong Yang & Huifang Shang. (2015) Depression and anxiety in amyotrophic lateral sclerosis: Correlations between the distress of patients and caregivers. Muscle & Nerve 51:3, pages 353-357.
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Takamura Nagasaka & Yoshihisa Takiyama. 2015. Neurodegenerative Disorders as Systemic Diseases. Neurodegenerative Disorders as Systemic Diseases 237 275 .
Janusz Surzykiewicz. 2015. Dem Gutes tun, der leidet. Dem Gutes tun, der leidet 101 125 .
G. Lucchetti, A. L. G. Lucchetti, G. R. Oliveira, D. Crispim, S. L. Pires, M. L. Gorzoni, C. R. G. Panicio & H. G. Koenig. (2014) Nursing home care: exploring the role of religiousness in the mental health, quality of life and stress of formal caregivers. Journal of Psychiatric and Mental Health Nursing 21:5, pages 403-413.
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Samar M Aoun, Brenda Bentley, Laura Funk, Chris Toye, Gunn Grande & Kelli J Stajduhar. (2012) A 10-year literature review of family caregiving for motor neurone disease: Moving from caregiver burden studies to palliative care interventions. Palliative Medicine 27:5, pages 437-446.
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. (2012) Current World Literature. Current Opinion in Supportive & Palliative Care 6:3, pages 402-416.
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Orla Hardiman, Leonard H. van den Berg & Matthew C. Kiernan. (2011) Clinical diagnosis and management of amyotrophic lateral sclerosis. Nature Reviews Neurology 7:11, pages 639-649.
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Myoung Soo KimHyung-Ik ShinYusun MinJung Yoon KimJung Soon Kim. (2011) Correlation between Severe ALS Patient-Caregiver Couples' Characteristics and Caregivers' Health Related Quality of Life. Journal of Korean Academy of Nursing 41:3, pages 354.
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