Citations (19)
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Cathryn Pinto, Adam W. A. Geraghty, Charlotte McLoughlin, Francesco Pagnini, Lucy Yardley & Laura Dennison. (2023) Experiences of psychological interventions in neurodegenerative diseases: a systematic review and thematic synthesis. Health Psychology Review 17:3, pages 416-438.
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Robert Simpson, Sharon Simpson, Marina Wasilewski, Stewart Mercer & Maggie Lawrence. (2022) Mindfulness-based interventions for people with multiple sclerosis: a systematic review and meta-aggregation of qualitative research studies. Disability and Rehabilitation 44:21, pages 6179-6193.
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Francesco Pagnini, Deborah Phillips, Anne Haulman, Matthew Bankert, Zachary Simmons & Ellen Langer. (2022) An online non-meditative mindfulness intervention for people with ALS and their caregivers: a randomized controlled trial. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 23:1-2, pages 116-127.
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Nicolò Zarotti, Emily Mayberry, Noora Ovaska-Stafford, Fiona Eccles & Jane Simpson. (2021) Psychological interventions for people with motor neuron disease: a scoping review. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 22:1-2, pages 1-11.
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Priya Treesa Thomas, Manjusha G. Warrier, Arun Sadasivan, Bhuvaneshwari Balasubramanium, Veeramani Preethish-kumar, Saraswati Nashi, Kiran Polavarapu, Gopalkrishna Krishna, Seena Vengalil, Prakashi Rajaram & Atchayaram Nalini. (2018) Caregiver burden and quality of life of patients with amyotrophic lateral sclerosis in India. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 19:7-8, pages 606-610.
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Articles from other publishers (14)
Paul Cafarella, Tanja Effing & Anna Chur-Hansen. (2022) Interventions targeting psychological well-being for motor neuron disease carers: A systematic review. Palliative and Supportive Care 21:2, pages 320-336.
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Cathryn Pinto, Adam W. A. Geraghty, Francesco Pagnini, Lucy Yardley & Laura Dennison. (2023) How do people with MND and caregivers experience a digital mental health intervention? A qualitative study. Frontiers in Psychiatry 14.
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Éilís Conroy, Polly Kennedy, Mark Heverin, Orla Hardiman & Miriam Galvin. (2023) Care, burden and self-described positive aspects of caring in amyotrophic lateral sclerosis: an exploratory, longitudinal, mixed-methods study. BMJ Open 13:1, pages e064254.
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Sandra L. Neate, Jeanette C. Reece, Craig Hassed, Richard Chambers, Sherelle Connaughton & Nupur Nag. (2022) A qualitative analysis of free text comments of participants from a massive open online mindfulness course. Frontiers in Public Health 10.
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Vittoria Anita Bilenchi, Paolo Banfi, Francesco Pagnini & Eleonora Volpato. (2022) Psychoeducational groups for people with Amyotrophic Lateral Sclerosis and their caregiver: a qualitative study. Neurological Sciences 43:7, pages 4239-4255.
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Jenny Murfield, Wendy Moyle & Analise O'Donovan. (2021) Mindfulness- and compassion-based interventions for family carers of older adults: A scoping review. International Journal of Nursing Studies 116, pages 103495.
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Nicolò Zarotti, Maria Dale, Fiona Eccles & Jane Simpson. (2020) Psychological Interventions for People with Huntington’s Disease: A Call to Arms. Journal of Huntington's Disease 9:3, pages 231-243.
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Danielle B. Rice, Andrea Carboni-Jiménez, Mara Cañedo-Ayala, Kimberly A. Turner, Matthew Chiovitti, Alexander W. Levis & Brett D. Thombs. (2020) Perceived Benefits and Facilitators and Barriers to Providing Psychosocial Interventions for Informal Caregivers of People with Rare Diseases: A Scoping Review. The Patient - Patient-Centered Outcomes Research 13:5, pages 471-519.
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Ben Parkinson, Maggie Lawrence, Evelyn McElhinney & Jo Booth. (2019) Mindfulness for people with long-term conditions and their family caregivers: A systematic review. Complementary Therapies in Clinical Practice 34, pages 76-86.
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Petter Sandstedt, Susanne Littorin, Gunilla Cröde Widsell, Sverker Johansson, Kristina Gottberg, Charlotte Ytterberg, Mariann Olsson, Lotta Widén Holmqvist & Marie Kierkegaard. (2018) Caregiver experience, health-related quality of life and life satisfaction among informal caregivers to patients with amyotrophic lateral sclerosis: A cross-sectional study. Journal of Clinical Nursing 27:23-24, pages 4321-4330.
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Tom Burke, Orla Hardiman, Marta Pinto-Grau, Katie Lonergan, Mark Heverin, Katy Tobin, Anthony Staines, Miriam Galvin & Niall Pender. (2018) Longitudinal predictors of caregiver burden in amyotrophic lateral sclerosis: a population-based cohort of patient–caregiver dyads. Journal of Neurology 265:4, pages 793-808.
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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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F. Pagnini, A. Marconi, A. Tagliaferri, G. M. Manzoni, R. Gatto, V. Fabiani, G. Gragnano, G. Rossi, E. Volpato, P. Banfi, A. Palmieri, F. Graziano, G. Castelnuovo, M. Corbo, E. Molinari, N. Riva, V. Sansone & C. Lunetta. (2017) Meditation training for people with amyotrophic lateral sclerosis: a randomized clinical trial. European Journal of Neurology 24:4, pages 578-586.
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Cesare Cavalera, Francesco Pagnini, Marco Rovaris, Laura Mendozzi, Luigi Pugnetti, Massimo Garegnani & Enrico Molinari. (2016) A telemedicine meditation intervention for people with multiple sclerosis and their caregivers: study protocol for a randomized controlled trial. Trials 17:1.
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