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Gepubliceerd in: Quality of Life Research 5/2015

01-05-2015 | Patient Engagement Special Section

Building new roles and relationships in research: a model of patient engagement research

Auteurs: Nancy Marlett, Svetlana Shklarov, Deborah Marshall, Maria Jose Santana, Tracy Wasylak

Gepubliceerd in: Quality of Life Research | Uitgave 5/2015

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Abstract

Purpose

Patient engagement is influenced by institutional ideologies, professional attitudes and patient readiness to accept new, engaged roles. This article provides an opportunity to consider a new role for patients who are trained to conduct patient experience research using qualitative methods.

Methods

The emergence of the role of patient engagement researcher was studied using a grounded theory with 21 patients over one-year internship and 125 research participants. Data were collected using tape recordings, field notes and student assignments. These were analyzed using open and selective coding, memoing, categorizing themes.

Results

Patients’ education level (from high school to PhD), cultural background (immigrant experience, seniors), employment (employed full or part time, receiving disability benefits or retired), age (late 30 s—75) and gender (17 women and four men) were diverse. Main categories (emancipating patient experience; qualifying for research; leading sitting down; working data together; seeding change) are organized by the dialectic of co-creation as the roles of patient and researcher merge. A theoretical model is proposed.

Discussion

The theoretical model provides a glimpse into the process of merging two distinct roles of patient and researcher and in the process unleashes a force for change.

Conclusions

The emergence of a dialectic from polar opposite roles is difficult to locate in health or other institutions where power differentials exist but there are indications that this new role might become a template for other merged roles in patient-led medical teams.
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Alleen toegankelijk voor geautoriseerde gebruikers
Literatuur
4.
go back to reference Domecq, J. P., Prutzky, G., Elryiah, T., Wong, Z., et al. (2014). Patient engagement in research: A systematic review. BMC Health Services Research, 14, 89.CrossRefPubMedCentralPubMed Domecq, J. P., Prutzky, G., Elryiah, T., Wong, Z., et al. (2014). Patient engagement in research: A systematic review. BMC Health Services Research, 14, 89.CrossRefPubMedCentralPubMed
8.
go back to reference Gallivan, J., Kovacs Burns, K. A., Bellows, M., Eigensehe, C. (2012) The many faces of patient engagement. The Journal of Participatory Medicine, 4, e32. Gallivan, J., Kovacs Burns, K. A., Bellows, M., Eigensehe, C. (2012) The many faces of patient engagement. The Journal of Participatory Medicine, 4, e32.
9.
go back to reference Gauvin, F. P. (2010). Patient and service user engagement: An environmental scan. Report submitted to the Canadian Health Services Research Foundation. Gauvin, F. P. (2010). Patient and service user engagement: An environmental scan. Report submitted to the Canadian Health Services Research Foundation.
10.
go back to reference Staniszewska, S., Denegri, S. (2013) Patient and public involvement in research: Future challenges. Evidence Based Nursing, 16(3), 69. Staniszewska, S., Denegri, S. (2013) Patient and public involvement in research: Future challenges. Evidence Based Nursing, 16(3), 69.
11.
go back to reference Devine, E. B., et al. (2013). A model for incorporating patient and stakeholder voices in a learning health care network: Washington State’s Comparative Effectiveness Research Translation Network. Journal of Clinical Epidemiology, 66(8 Suppl), 122–129.CrossRef Devine, E. B., et al. (2013). A model for incorporating patient and stakeholder voices in a learning health care network: Washington State’s Comparative Effectiveness Research Translation Network. Journal of Clinical Epidemiology, 66(8 Suppl), 122–129.CrossRef
12.
go back to reference Glaser, B. G., & Strauss, A. L. (1967). The discovery of grounded theory. Strategies for qualitative research. New Jersey: Aldine Transaction, Inc. Network. Glaser, B. G., & Strauss, A. L. (1967). The discovery of grounded theory. Strategies for qualitative research. New Jersey: Aldine Transaction, Inc. Network.
13.
go back to reference Charmaz, K. (2006). Constructing grounded theory. Thousand Oaks, CA: Sage. Charmaz, K. (2006). Constructing grounded theory. Thousand Oaks, CA: Sage.
14.
go back to reference Strauss, A., & Corbin, J. (1998). Basics of qualitative research: Techniques and procedures for developing grounded theory. Thousand Oaks, CA: Sage. Strauss, A., & Corbin, J. (1998). Basics of qualitative research: Techniques and procedures for developing grounded theory. Thousand Oaks, CA: Sage.
15.
go back to reference Glaser, B. G. (2001). The grounded theory perspective: Conceptualization contrasted with description. Mill Valley, CA: Sociology Press. Glaser, B. G. (2001). The grounded theory perspective: Conceptualization contrasted with description. Mill Valley, CA: Sociology Press.
16.
go back to reference Glaser, B. G. (2003). The grounded theory perspective II: Description’s remodeling of Grounded Theory methodology. Mill Valley, CA: Sociology Press. Glaser, B. G. (2003). The grounded theory perspective II: Description’s remodeling of Grounded Theory methodology. Mill Valley, CA: Sociology Press.
17.
go back to reference Glaser, B. G. (2005). The grounded theory perspective III: Theoretical coding. Mill Valley, CA: Sociology Press. Glaser, B. G. (2005). The grounded theory perspective III: Theoretical coding. Mill Valley, CA: Sociology Press.
18.
go back to reference Hernandez, C.A. (1991). The lived experience of Type 1 diabetes: Implications for diabetes education. Unpublished doctoral dissertation, University of Toronto, Toronto, Canada. Hernandez, C.A. (1991). The lived experience of Type 1 diabetes: Implications for diabetes education. Unpublished doctoral dissertation, University of Toronto, Toronto, Canada.
19.
go back to reference Bryant, A., & Charmaz, K. (2007). Handbook of grounded theory. London: Sage. Bryant, A., & Charmaz, K. (2007). Handbook of grounded theory. London: Sage.
20.
go back to reference Charmaz, K. (2014). Constructing grounded theory: A practical guide through qualitative analysis (Introducing Qualitative series), 2nd edn. Thousand Oaks, CA: Sage. Charmaz, K. (2014). Constructing grounded theory: A practical guide through qualitative analysis (Introducing Qualitative series), 2nd edn. Thousand Oaks, CA: Sage.
21.
go back to reference Morse, J. M., Stern, P. N., Corbin, J., Bowers, B., Charmaz, K., Clarke, A. E. (2009). Developing grounded theory: The second generation. California: Left Coast Press. Morse, J. M., Stern, P. N., Corbin, J., Bowers, B., Charmaz, K., Clarke, A. E. (2009). Developing grounded theory: The second generation. California: Left Coast Press.
23.
go back to reference Mays, N., Pope, C. (1995). Qualitative research: Observational methods in health care settings. British Medical Journal, 311, 182. Mays, N., Pope, C. (1995). Qualitative research: Observational methods in health care settings. British Medical Journal, 311, 182.
24.
go back to reference Corbin, J., Strauss, A. (2007). Basics of qualitative research. Thousand Oaks, CA: Sage. Corbin, J., Strauss, A. (2007). Basics of qualitative research. Thousand Oaks, CA: Sage.
26.
go back to reference Shklarov, S., Wasylak, T., Marlett, N., Marshall, D., Noseworthy, T. (2013). Patients matter: Engaging patients as collaborators to improve osteoarthritis (OA) care in Alberta. Final project report. Submitted to the Canadian Foundation for Healthcare Improvement.www.ucalgary.ca. Access 23 July. Shklarov, S., Wasylak, T., Marlett, N., Marshall, D., Noseworthy, T. (2013). Patients matter: Engaging patients as collaborators to improve osteoarthritis (OA) care in Alberta. Final project report. Submitted to the Canadian Foundation for Healthcare Improvement.www.​ucalgary.​ca. Access 23 July.
27.
go back to reference Staniszewska, S., Haywood, K. L., Brett, J., & Tutton, L. (2012). Patient and public involvement in patient-reported outcome measures: Evolution not revolution. Patient, 5(2), 79–87.CrossRefPubMed Staniszewska, S., Haywood, K. L., Brett, J., & Tutton, L. (2012). Patient and public involvement in patient-reported outcome measures: Evolution not revolution. Patient, 5(2), 79–87.CrossRefPubMed
28.
go back to reference Nicklin, J., Cramp, F., Kirwan, J., Urban, M., Hewlett, S. (2010). Collaboration with patients in the design of patient-reported outcome measures: Capturing the experience of fatigue in rheumatoid arthritis. Arthritis Care Research (Hoboken), 62(11), 1552–1558. Nicklin, J., Cramp, F., Kirwan, J., Urban, M., Hewlett, S. (2010). Collaboration with patients in the design of patient-reported outcome measures: Capturing the experience of fatigue in rheumatoid arthritis. Arthritis Care Research (Hoboken), 62(11), 1552–1558.
Metagegevens
Titel
Building new roles and relationships in research: a model of patient engagement research
Auteurs
Nancy Marlett
Svetlana Shklarov
Deborah Marshall
Maria Jose Santana
Tracy Wasylak
Publicatiedatum
01-05-2015
Uitgeverij
Springer International Publishing
Gepubliceerd in
Quality of Life Research / Uitgave 5/2015
Print ISSN: 0962-9343
Elektronisch ISSN: 1573-2649
DOI
https://doi.org/10.1007/s11136-014-0845-y

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