IDEAS home Printed from https://ideas.repec.org/a/eee/socmed/v61y2005i2p431-441.html
   My bibliography  Save this article

Managing constraint: the experience of people with chronic pain

Author

Listed:
  • Miles, A.
  • Curran, H.V.
  • Pearce, S.
  • Allan, L.

Abstract

This study describes the experience of people with chronic pain. Using the method of grounded theory, 29 chronic pain sufferers were interviewed at an outpatient pain clinic. A model depicting the basic social psychological process of maintaining a normal life through constraint was developed. This process revolved around people's perception of the constraints imposed by pain: bodily constraint (constraint on the body and its relationship to the environment); activity constraint (the constraint on what people could do); and identity constraint (the constraint on what people could be). The degree to which pain had challenged what people had previously accepted as 'normal' was illustrated through their evaluation of the impact of pain. The conclusion of this process of evaluation reflected how people coped with the constraints of pain-whether they were assimilated, accommodated, confronted or subverted. In assimilation, the constraints were absorbed and normal life maintained. In accommodation, the constraints were accepted and normal life re-defined. In confrontation, the constraints were rejected and pre-pain identities and activities pursued despite leading to increased pain levels. In subversion, attempts were made to retain pre-pain identities, and although pain levels were minimized, activities were altered to a significant degree. The limitations imposed by pain often form the focus of people's coping efforts, rather than the pain per se. The desire to retain pre-pain 'normal' lifestyles may underlie people's use of coping strategies that exacerbate pain intensity and pain-related disability. Future research needs to explore both the relationship between adjustment to pain and adjustment to the restrictions associated with ageing, and the role of body techniques and identity management in adjustment to pain in order to understand factors which may promote pain acceptance.

Suggested Citation

  • Miles, A. & Curran, H.V. & Pearce, S. & Allan, L., 2005. "Managing constraint: the experience of people with chronic pain," Social Science & Medicine, Elsevier, vol. 61(2), pages 431-441, July.
  • Handle: RePEc:eee:socmed:v:61:y:2005:i:2:p:431-441
    as

    Download full text from publisher

    File URL: http://www.sciencedirect.com/science/article/pii/S0277-9536(04)00650-1
    Download Restriction: Full text for ScienceDirect subscribers only
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    References listed on IDEAS

    as
    1. Lillrank, Annika, 2003. "Back pain and the resolution of diagnostic uncertainty in illness narratives," Social Science & Medicine, Elsevier, vol. 57(6), pages 1045-1054, September.
    2. Risdon, Andrea & Eccleston, Chris & Crombez, Geert & McCracken, Lance, 2003. "How can we learn to live with pain? A Q-methodological analysis of the diverse understandings of acceptance of chronic pain," Social Science & Medicine, Elsevier, vol. 56(2), pages 375-386, January.
    Full references (including those not matched with items on IDEAS)

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Sim, Julius & Madden, Sue, 2008. "Illness experience in fibromyalgia syndrome: A metasynthesis of qualitative studies," Social Science & Medicine, Elsevier, vol. 67(1), pages 57-67, July.

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Melander, Stina, 2023. "Different logics of pain: the gendered dimension of chronic pain in a relational setting," Social Science & Medicine, Elsevier, vol. 335(C).
    2. Richardson, Jane C. & Ong, Bie Nio & Sim, Julius, 2006. "Is chronic widespread pain biographically disruptive?," Social Science & Medicine, Elsevier, vol. 63(6), pages 1573-1585, September.
    3. Baker, Rachel Mairi, 2006. "Economic rationality and health and lifestyle choices for people with diabetes," Social Science & Medicine, Elsevier, vol. 63(9), pages 2341-2353, November.
    4. Paul Atkinson, 2009. "Illness Narratives Revisited: The Failure of Narrative Reductionism," Sociological Research Online, , vol. 14(5), pages 196-205, November.
    5. N. Exel & G. Graaf & P. Rietveld, 2011. "“I can do perfectly well without a car!”," Transportation, Springer, vol. 38(3), pages 383-407, May.
    6. Inge M Brokerhof & Jan Fekke Ybema & P Matthijs Bal, 2020. "Illness narratives and chronic patients’ sustainable employability: The impact of positive work stories," PLOS ONE, Public Library of Science, vol. 15(2), pages 1-17, February.
    7. van Exel, Job & de Graaf, Gjalt & Brouwer, Werner, 2008. "Give me a break!: Informal caregiver attitudes towards respite care," Health Policy, Elsevier, vol. 88(1), pages 73-87, October.
    8. Corbett, Mandy & Foster, Nadine E. & Ong, Bie Nio, 2007. "Living with low back pain--Stories of hope and despair," Social Science & Medicine, Elsevier, vol. 65(8), pages 1584-1594, October.
    9. Hunter, William Cannon, 2011. "Rukai indigenous tourism: Representations, cultural identity and Q method," Tourism Management, Elsevier, vol. 32(2), pages 335-348.
    10. Dumit, Joseph, 2006. "Illnesses you have to fight to get: Facts as forces in uncertain, emergent illnesses," Social Science & Medicine, Elsevier, vol. 62(3), pages 577-590, February.
    11. van Exel, N.J.A. & de Graaf, G. & Brouwer, W.B.F., 2006. ""Everyone dies, so you might as well have fun!" Attitudes of Dutch youths about their health lifestyle," Social Science & Medicine, Elsevier, vol. 63(10), pages 2628-2639, November.
    12. Weldegiorgis, Fitsum S. & Ali, Saleem H., 2016. "Mineral resources and localised development: Q-methodology for rapid assessment of socioeconomic impacts in Rwanda," Resources Policy, Elsevier, vol. 49(C), pages 1-11.
    13. van Exel, Job & Baker, Rachel & Mason, Helen & Donaldson, Cam & Brouwer, Werner, 2015. "Public views on principles for health care priority setting: Findings of a European cross-country study using Q methodology," Social Science & Medicine, Elsevier, vol. 126(C), pages 128-137.
    14. Jeffrey E Black & Kathrin Kopke & Cathal O’Mahony, 2019. "Towards a Circular Economy: Using Stakeholder Subjectivity to Identify Priorities, Consensus, and Conflict in the Irish EPS/XPS Market," Sustainability, MDPI, vol. 11(23), pages 1-20, December.
    15. Koekkoek, B. & Hutschemaekers, G. & van Meijel, B. & Schene, A., 2011. "How do patients come to be seen as 'difficult'?: A mixed-methods study in community mental health care," Social Science & Medicine, Elsevier, vol. 72(4), pages 504-512, February.
    16. Allan Guzman & Kreziah Silva & Julienne Silvestre & Jenika Simbillo & Jan Simpauco & Reuben Sinugbuhan & Donna Sison & Marielle Siy, 2012. "For your Eyes Only: A Q-Methodology on the Ontology of Happiness Among Chronically Ill Filipino Elderly in a Penal Institution," Journal of Happiness Studies, Springer, vol. 13(5), pages 913-930, October.
    17. Costa, Nathalia & Mescouto, Karime & Dillon, Miriam & Olson, Rebecca & Butler, Prudence & Forbes, Roma & Setchell, Jenny, 2022. "The ubiquity of uncertainty in low back pain care," Social Science & Medicine, Elsevier, vol. 313(C).
    18. Kielmann, Karina & Deshmukh, Deepali & Deshpande, Sucheta & Datye, Vinita & Porter, John & Rangan, Sheela, 2005. "Managing uncertainty around HIV/AIDS in an urban setting: Private medical providers and their patients in Pune, India," Social Science & Medicine, Elsevier, vol. 61(7), pages 1540-1550, October.
    19. Willig, Carla, 2011. "Cancer diagnosis as discursive capture: Phenomenological repercussions of being positioned within dominant constructions of cancer," Social Science & Medicine, Elsevier, vol. 73(6), pages 897-903, September.
    20. Sung Soo Lim, 2020. "The Effects of Chronic Illness on Aspirations and Subjective Wellbeing," Journal of Happiness Studies, Springer, vol. 21(5), pages 1771-1793, June.

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:eee:socmed:v:61:y:2005:i:2:p:431-441. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Catherine Liu (email available below). General contact details of provider: http://www.elsevier.com/wps/find/journaldescription.cws_home/315/description#description .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.