A Non-Randomized Comparison of Online and In-Person Formats of the Canadian Androgen Deprivation Therapy Educational Program: Impacts on Side Effects, Bother, and Self-Efficacy

Author:

Walker Lauren M.12,Sears Carly S.1ORCID,Wibowo Erik3,Robinson John W.1,Matthew Andrew G.4,McLeod Deborah L.5,Wassersug Richard J.6ORCID

Affiliation:

1. Division of Psychosocial Oncology, Department of Oncology, University of Calgary, Calgary, AB T2N 4N1, Canada

2. Arnie Charbonneau Cancer Institute, University of Calgary, Calgary, AB T2N 4N1, Canada

3. School of Medical Sciences, Faculty of Medicine and Health, University of Sydney, Sydney 2006, Australia

4. Division of Urology, Department of Surgery, University of Toronto, Toronto, ON M5T 2SB, Canada

5. School of Nursing, Faculty of Health, Dalhousie University, Halifax, NS B3H 4R2, Canada

6. Cellular & Physiological Sciences, Faculty of Medicine, University of British Columbia, Vancouver, BC V6T 2A1, Canada

Abstract

Although Androgen Deprivation Therapy (ADT) is effective in controlling prostate cancer (PCa) and increasing survival, it is associated with a myriad of side effects that cause significant morbidity. Previous research has shown that PCa patients starting on ADT are neither fully informed nor well-equipped to manage the breadth of ADT’s side effects. The ADT Educational Program (a 1.5 h interactive class plus a book) was developed as an evidence-based resource for patients dealing with ADT. Our aim here was to compare the efficacy of an online version of the class with a previously assessed in-person version of the class. Using mixed MANOVAs within a non-randomized comparison design, we assessed: (1) changes in patients’ experiences of self-efficacy to manage and bother associated with side effects approximately 10 weeks after attending a class, and (2) potential differences in these variables between online and in-person class formats. Side effect bother decreased from pre- to post-class but did not differ between in-person (n = 94) and online (n = 137) class cohorts. While self-efficacy to manage side effects was slightly higher post-class in both cohorts, the increase was not statistically significant. Average self-efficacy ratings were significantly higher among in-person versus online class participants (p < 0.05; ηp2 = 0.128). Both online and in-person classes are associated with a significant reduction in the severity of side effect bother reported by PCa patients, suggesting non-inferiority of online versus in-person formats. Online classes offer greater accessibility to the program for patients outside the reach of in-person classes, increasing the availability of the program to more PCa patients and family members across Canada.

Funder

Astellas Pharma Inc.

Tolmar Pharmaceuticals Inc.

Calgary Prostate Cancer Centre

Publisher

MDPI AG

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