Citations (35)
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Nicola Glennie, Fiona M. Harris & Emma F. France. (2023) Perceptions and experiences of control among people living with motor neurone disease: a systematic review and thematic synthesis. Disability and Rehabilitation 45:16, pages 2554-2566.
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Nicolò Zarotti, Katherine Helen O’Leary Deane, Catherine Elaine Longworth Ford & Jane Simpson. (2023) Perceived control as a predictor of medication adherence in people with Parkinson’s: a large-scale cross-sectional study. Disability and Rehabilitation 0:0, pages 1-11.
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Nicolò Zarotti, Katherine Helen O’Leary Deane, Catherine Elaine Longworth Ford & Jane Simpson. (2023) Psychosocial interventions affecting global perceptions of control in people with Parkinson’s disease: a scoping review. Disability and Rehabilitation 0:0, pages 1-10.
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Eleftherios Anestis, Fiona J. R. Eccles, Ian Fletcher, Sofia Triliva & Jane Simpson. (2022) Healthcare professionals’ involvement in breaking bad news to newly diagnosed patients with motor neurodegenerative conditions: a qualitative study. Disability and Rehabilitation 44:25, pages 7877-7890.
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Gina Wieringa, Maria Dale & Fiona J. R. Eccles. (2022) Adjusting to living with Parkinson’s disease; a meta-ethnography of qualitative research. Disability and Rehabilitation 44:23, pages 6949-6968.
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Dagmar Amtmann, Alyssa M. Bamer, Mara B. Nery-Hurwit, Kendra S. Liljenquist & Kathryn Yorkston. (2019) Factors associated with disease self-efficacy in individuals aging with a disability. Psychology, Health & Medicine 24:10, pages 1171-1181.
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Laurence Regan, Nancy J. Preston, Fiona J. R. Eccles & Jane Simpson. (2019) The views of adults with neurodegenerative diseases on end-of-life care: a metasynthesis. Aging & Mental Health 23:2, pages 149-157.
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Kriten Mistry & Jane Simpson. (2013) Exploring the transitional process from receiving a diagnosis to living with motor neurone disease. Psychology & Health 28:8, pages 939-953.
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Articles from other publishers (27)
V. Stopic, A. Rizos, J. Simpson, F. J. R. Eccles, T. A. Dembek, M. T. Barbe & A. Sauerbier. (2023) Interkulturelle Adaptation der PUKSoPC in deutscher SpracheIntercultural adaptation of the PUKSoPC in German language. Der Nervenarzt.
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Ian W. Garner, Craig D. Murray, Fiona J. R. Eccles, Nicolò Zarotti & Jane Simpson. (2023) “I Feel Like I Work Full-Time for Parkinson’s”: A Longitudinal Interpretative Phenomenological Analysis of the Experiences of Parkinson’s Informal Caregivers during COVID-19 in England. NeuroSci 4:2, pages 105-117.
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Erika Wright, Timothy R. Elliott, Oi‐Man Kwok, Qiyue Zhang & Mikaela Spooner. (2023) Resilience and distress among young adults with chronic health conditions: A longitudinal study. British Journal of Health Psychology.
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Marta Rzadkiewicz, Mariusz Jaworski & Dorota Włodarczyk. (2022) The Brave Patient after 80—Satisfaction with Visit and Individual Determinants of Proactive Patient Attitude among the Oldest General Practice Users. International Journal of Environmental Research and Public Health 19:10, pages 6214.
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Nicolò Zarotti, Maria Dale, Fiona J. R. Eccles & Jane Simpson. (2022) More than Just a Brain Disorder: A Five-Point Manifesto for Psychological Care for People with Huntington’s Disease. Journal of Personalized Medicine 12:1, pages 64.
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Nicolò Zarotti, Fiona J. R. Eccles, Jennifer A. Foley, Andrew Paget, Sarah Gunn, Iracema Leroi & Jane Simpson. (2020) Psychological interventions for people with Parkinson’s disease in the early 2020s: Where do we stand?. Psychology and Psychotherapy: Theory, Research and Practice 94:3, pages 760-797.
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Ingrid Estrada-Bellmann, Jesús Daniel Meléndez-Flores, Carlos Rodrigo Cámara-Lemarroy & Sergio Andrés Castillo-Torres. (2021) Determinants of self-efficacy in patients with Parkinson’s disease. Arquivos de Neuro-Psiquiatria 79:8, pages 686-691.
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Fiona J.R. Eccles, David Craufurd, Alistair Smith, Rhys Davies, Kristian Glenny, Max Homberger, Leona Rose, Rachael Theed, Siofra Peeren, Dawn Rogers, Zara Skitt, Nicolò Zarotti & Jane Simpson. (2021) Experiences of Mindfulness-Based Cognitive Therapy for Premanifest Huntington’s Disease. Journal of Huntington's Disease 10:2, pages 277-291.
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Ingeborg Halse, Guro Hanevold Bjørkløf, Knut Engedal, Geir Selbæk & Maria Lage Barca. (2021) Locus of Control and Its Associations with Depressive Symptoms amongst People with Dementia. Dementia and Geriatric Cognitive Disorders 50:3, pages 258-265.
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Joanna Dymecka, Rafał Gerymski & Mariola Bidzan. (2020) Selected psychometric aspects of the Polish version of the Liverpool Self-efficacy Scale. Current Issues in Personality Psychology 8:4, pages 339-351.
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Dr. Lauren Strober. (2020) Determinants of unemployment in multiple sclerosis (MS): The role of disease, person-specific factors, and engagement in positive health-related behaviors. Multiple Sclerosis and Related Disorders 46, pages 102487.
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Danielle Verity, Fiona J.R. Eccles, Amanda Boland & Jane Simpson. (2020) Does perceived control mediate the relationship between stigma and well-being for individuals with Parkinson's disease?. Journal of the Neurological Sciences 414, pages 116841.
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Nicolò Zarotti, Elizabeth Coates, Alex McGeachan, Isobel Williams, Daniel Beever, Gemma Hackney, Paul Norman, Theocharis Stavroulakis, David White, Sean White, Vanessa Halliday & Christopher McDermott. (2019) Health care professionals’ views on psychological factors affecting nutritional behaviour in people with motor neuron disease: A thematic analysis. British Journal of Health Psychology 24:4, pages 953-969.
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Alice K. Carter, Lauren J. Breen & Janet M. Beilby. (2019) Self-efficacy beliefs: Experiences of adults who stutter. Journal of Fluency Disorders 60, pages 11-25.
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Diana S Dorstyn, Rachel M Roberts, Gregory Murphy & Rebecca Haub. (2017) Employment and multiple sclerosis: A meta-analytic review of psychological correlates. Journal of Health Psychology 24:1, pages 38-51.
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L.B. Strober. (2018) Quality of life and psychological well-being in the early stages of multiple sclerosis (MS): Importance of adopting a biopsychosocial model. Disability and Health Journal 11:4, pages 555-561.
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Jane Simpson, Gerasimos Chatzidamianos, Ian Fletcher, Luis Perpetuo & Fiona J R Eccles. (2018) A new scale measuring adaptive perceived control for people with Parkinson's: Initial construction and further validation. Journal of the Neurological Sciences 391, pages 77-83.
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Lauren B. Strober, Nancy Chiaravalloti & John DeLuca. (2018) Should I stay or should I go? A prospective investigation examining individual factors impacting employment status among individuals with multiple sclerosis (MS). Work 59:1, pages 39-47.
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Alice Carter, Lauren Breen, J. Scott Yaruss & Janet Beilby. (2017) Self-efficacy and quality of life in adults who stutter. Journal of Fluency Disorders 54, pages 14-23.
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Jack K. Garlovsky, Paul G. Overton & Jane Simpson. (2016) Psychological Predictors of Anxiety and Depression in Parkinson's Disease: A Systematic Review. Journal of Clinical Psychology 72:10, pages 979-998.
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Lauren B. Strober, Allison Binder, Olga M. Nikelshpur, Nancy Chiaravalloti & John DeLuca. (2016) The Perceived Deficits Questionnaire. International Journal of MS Care 18:4, pages 183-190.
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Stephen Krieger, Shawn F. Sorrells, Molly Nickerson & Thaddeus W.W. Pace. (2014) Mechanistic insights into corticosteroids in multiple sclerosis: War horse or chameleon?☆. Clinical Neurology and Neurosurgery 119, pages 6-16.
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Maren GalushkoHeidrun GollaJulia StruppUte KarbachClaudia KaiserNicole ErnstmannHolger PfaffChristoph OstgatheRaymond Voltz. (2014) Unmet Needs of Patients Feeling Severely Affected by Multiple Sclerosis in Germany: A Qualitative Study. Journal of Palliative Medicine 17:3, pages 274-281.
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Adam B. Levin, Emily J. Hadgkiss, Tracey J. Weiland & George A. Jelinek. (2014) Meditation as an Adjunct to the Management of Multiple Sclerosis. Neurology Research International 2014, pages 1-10.
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E. Gaëlle Hortop, Carsten Wrosch & Marylène Gagné. (2013) The why and how of goal pursuits: Effects of global autonomous motivation and perceived control on emotional well-being. Motivation and Emotion 37:4, pages 675-687.
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Jane Simpson, Godwin Lekwuwa & Trevor Crawford. (2013) Illness beliefs and psychological outcome in people with Parkinson’s disease. Chronic Illness 9:2, pages 165-176.
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Melanie Keeling, Jacki Bambrough & Jane Simpson. (2012) Depression, anxiety and positive affect in people diagnosed with low‐grade tumours: the role of illness perceptions. Psycho-Oncology 22:6, pages 1421-1427.
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