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Reconsidering patient empowerment in chronic illness: A critique of models of self-efficacy and bodily control

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  • Aujoulat, Isabelle
  • Marcolongo, Renzo
  • Bonadiman, Leopoldo
  • Deccache, Alain

Abstract

Studies that focus on patient empowerment tend to address more specifically two issues of patients' experience of illness: managing regimens and relating to health-care providers. Other aspects of illness experience, such as coming to terms with disrupted identities, tend to be overlooked. The outcome of empowerment is therefore usually referred to as achieving self-efficacy, mastery and control. We conducted an inductive exploratory study, based on individual in-depth interviews with 40 chronically ill patients in Belgium and Italy, in order to understand the process of empowerment as it may occur in patients whose experience of illness has at some point induced a feeling of powerlessness, which we conceptualised as a threat to their senses of security and identity. Our findings show that empowerment and control are not one and the same thing. We describe patient empowerment as a process of personal transformation which occurs through a double process of (i) "holding on" to previous self-representations and roles and learning to control the disease and treatment, so as to differentiate one's self from illness on the one hand, and on the other hand (ii) "letting go", by accepting to relinquish control, so as to integrate illness and illness-driven boundaries as being part of a reconciled self. Whereas the process of separating identities ("holding on") was indeed found to be linked to efforts aimed at taking control and maintaining or regaining a sense of mastery, the process of reconciling identities ("letting go") was found to be linked to a need for coherence, which included a search for meaning and the acceptance that not everything is controllable. We argue that the process of relinquishing control is as central to empowerment as is the process of gaining control. As a "successful" process of empowerment occurs when patients come to terms with their threatened security and identity, not only with their treatment, it may be facilitated by health-care providers through the use of narratives.

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  • Aujoulat, Isabelle & Marcolongo, Renzo & Bonadiman, Leopoldo & Deccache, Alain, 2008. "Reconsidering patient empowerment in chronic illness: A critique of models of self-efficacy and bodily control," Social Science & Medicine, Elsevier, vol. 66(5), pages 1228-1239, March.
  • Handle: RePEc:eee:socmed:v:66:y:2008:i:5:p:1228-1239
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    1. Clarke, Juanne N. & James, Susan, 2003. "The radicalized self: the impact on the self of the contested nature of the diagnosis of chronic fatigue syndrome," Social Science & Medicine, Elsevier, vol. 57(8), pages 1387-1395, October.
    2. Adams, Stephanie & Pill, Roisin & Jones, Alan, 1997. "Medication, chronic illness and identity: The perspective of people with asthma," Social Science & Medicine, Elsevier, vol. 45(2), pages 189-201, July.
    3. Albrecht, Gary L. & Devlieger, Patrick J., 1999. "The disability paradox: high quality of life against all odds," Social Science & Medicine, Elsevier, vol. 48(8), pages 977-988, April.
    4. Nochi, Masahiro, 2000. "Reconstructing self-narratives in coping with traumatic brain injury," Social Science & Medicine, Elsevier, vol. 51(12), pages 1795-1804, December.
    5. Salmon, Peter & Hall, George M, 2003. "Patient empowerment and control: a psychological discourse in the service of medicine," Social Science & Medicine, Elsevier, vol. 57(10), pages 1969-1980, November.
    6. Conrad, Peter, 1990. "Qualitative research on chronic illness: A commentary on method and conceptual development," Social Science & Medicine, Elsevier, vol. 30(11), pages 1257-1263, January.
    7. Fife, Betsy L., 1995. "The measurement of meaning in illness," Social Science & Medicine, Elsevier, vol. 40(8), pages 1021-1028, April.
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    2. Jae-Mahn Shim, 2022. "Patient Agency: Manifestations of Individual Agency Among People With Health Problems," SAGE Open, , vol. 12(1), pages 21582440221, March.
    3. Giuseppe Russo & Andrea Moretta Tartaglione & Ylenia Cavacece, 2019. "Empowering Patients to Co-Create a Sustainable Healthcare Value," Sustainability, MDPI, vol. 11(5), pages 1-20, March.
    4. Radaelli, Giovanni & Lettieri, Emanuele & Frattini, Federico & Luzzini, Davide & Boaretto, Andrea, 2017. "Users' search mechanisms and risks of inappropriateness in healthcare innovations: The role of literacy and trust in professional contexts," Technological Forecasting and Social Change, Elsevier, vol. 120(C), pages 240-251.
    5. Fumagalli, Lia Paola & Radaelli, Giovanni & Lettieri, Emanuele & Bertele’, Paolo & Masella, Cristina, 2015. "Patient Empowerment and its neighbours: Clarifying the boundaries and their mutual relationships," Health Policy, Elsevier, vol. 119(3), pages 384-394.
    6. Mariam Kashani & Arn Eliasson & Elaine Walizer & Clarie Fuller & Renata Engler & Todd Villines & Marina Vernalis, 2016. "Early Empowerment Strategies Boost Self-Efficacy to Improve Cardiovascular Health Behaviors," Global Journal of Health Science, Canadian Center of Science and Education, vol. 8(9), pages 322-322, September.
    7. Tania Burchardt & Martin Evans & Holly Holder, 2012. "Measuring Inequality: Autonomy The degree of empowerment in decisions about one’s own life," CASE Reports casereport74, Centre for Analysis of Social Exclusion, LSE.
    8. Chiara Cant? & Alessandra Tzannis, 2016. "The service innovation in healthcare network," MERCATI & COMPETITIVIT?, FrancoAngeli Editore, vol. 2016(4), pages 109-130.
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    10. Sarianne Wiklund Axelsson & Åsa Wikberg-Nilsson & Anita Melander Wikman, 2016. "Sustainable Lifestyle Change—Participatory Design of Support Together with Persons with Obesity in the Third Age," IJERPH, MDPI, vol. 13(12), pages 1-13, December.

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