Cancer informational support and health care service use among individuals newly diagnosed: a mixed methods approach

Authors

  • Sylvie Dubois RN PhD,

    Corresponding author
    1. Assistant Professor, Faculty of Nursing, Montreal University, Montreal, Quebec, Canada
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  • Carmen G. Loiselle RN PhD

    1. Assistant Professor, School of Nursing, McGill University; Nurse Scientist, Centre for Nursing Research, SMBD Jewish General Hospital, Montreal, Quebec, Canada
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Sylvie Dubois
Faculty of Nursing
Montreal University
2375 Côte Ste-Catherine
Montreal
Quebec
Canada
H3T 1A8
E-mail: sylvie.dubois@umontreal.ca

Abstract

Aim  To report on the integration of quantitative and qualitative findings to increase understanding of the role of cancer informational support and use of health care services among individuals newly diagnosed with breast or prostate cancer.

Methods  A mixed methods sequential design was used. First, a quantitative secondary analysis considered self-report data from a large number of individuals newly diagnosed with cancer (n = 250); next, a follow-up, in-depth qualitative inquiry with distinct individuals also newly diagnosed was conducted (n = 20); last, using a quantitative-hierarchical strategy, quantitative and qualitative findings were merged and re-analyzed.

Results  Quantitative analyses showed significant relationships between informational support and health care services. For instance, individuals who received more intense cancer informational support [face-to-face and information technology (IT)] spent more time with nurses. Women with breast cancer as opposed to men with prostate cancer also were found to rely primarily on nurses for cancer information and information on health services available, whereas men relied mostly on their oncologists. In-depth interviews revealed that informational support could be construed as positive, unsupportive, or mixed depending on context. The mixed design analysis documented positive experiences for individuals who reported to be better prepared for consultations and treatments with information provided by more than one source. Negative experiences with physicians were reported by both women and men but the former was about quality of cancer information provided and the latter in terms of quantity.

Conclusions  A mixed methods approach allowed a deeper understanding of the role of informational support on subsequent use of health care services by individuals with cancer. Further studies may include other types of cancer and diverse background characteristics to clarify how informational support and subsequent use of health services may be jointly determined by these factors.

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