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Racial differences in user experiences and perceived value of electronic symptom monitoring in a cohort of black and white bladder and prostate cancer patients.

Publication ,  Journal Article
Samuel, CA; Smith, AB; Elkins, W; Richmond, J; Mahbooba, Z; Basch, E; Bennett, AV; Chung, AE; Jonsson, M; Chen, RC; Reeve, BB
Published in: Qual Life Res
November 2021

PURPOSE: Electronic patient-reported outcomes (ePROs) are increasingly being used for symptom monitoring during routine cancer care, but have rarely been evaluated in diverse patient populations. We assessed ePRO user experiences and perceived value among Black and White cancer patients. METHODS: We recruited 30 Black and 49 White bladder and prostate cancer patients from a single institution. Participants reported symptoms using either a web-based or automated telephone interface over 3 months and completed satisfaction surveys and qualitative interviews focused on user experiences and value. Using a narrative mixed methods approach, we evaluated overall and race-specific differences in ePRO user experiences and perceived value. RESULTS: Most participants selected the web-based system, but Blacks were more likely to use the automated telephone-based system than Whites. In satisfaction surveys, Whites more commonly reported ease in understanding and reporting symptoms compared with Blacks. Blacks more often reported that the ePRO system was helpful in facilitating symptom-related discussions with clinicians. During interviews, Blacks described how the ePRO helped them recognize symptoms, while Whites found value in better understanding and tracking symptoms longitudinally. Blacks also expressed preferences for paper-based ePRO options due to perceived ease in better understanding of symptom items. CONCLUSION: Electronic patient-reported outcomes are perceived as valuable for variable reasons by Black and White cancer populations, with greater perceived value for communicating with clinicians reported among Blacks. To optimize equitable uptake of ePROs, oncology practices should offer several ePRO options (e.g., web-based, phone-based), as well as paper-based options, and consider the e-health literacy needs of patients during implementation.

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Published In

Qual Life Res

DOI

EISSN

1573-2649

Publication Date

November 2021

Volume

30

Issue

11

Start / End Page

3213 / 3227

Location

Netherlands

Related Subject Headings

  • Urinary Bladder
  • Race Factors
  • Quality of Life
  • Prostatic Neoplasms
  • Patient Reported Outcome Measures
  • Male
  • Humans
  • Health Policy & Services
  • Electronics
  • 44 Human society
 

Citation

APA
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Samuel, C. A., Smith, A. B., Elkins, W., Richmond, J., Mahbooba, Z., Basch, E., … Reeve, B. B. (2021). Racial differences in user experiences and perceived value of electronic symptom monitoring in a cohort of black and white bladder and prostate cancer patients. Qual Life Res, 30(11), 3213–3227. https://doi.org/10.1007/s11136-020-02442-4
Samuel, Cleo A., Angela B. Smith, Wendi Elkins, Jennifer Richmond, Zahra Mahbooba, Ethan Basch, Antonia V. Bennett, et al. “Racial differences in user experiences and perceived value of electronic symptom monitoring in a cohort of black and white bladder and prostate cancer patients.Qual Life Res 30, no. 11 (November 2021): 3213–27. https://doi.org/10.1007/s11136-020-02442-4.
Samuel CA, Smith AB, Elkins W, Richmond J, Mahbooba Z, Basch E, et al. Racial differences in user experiences and perceived value of electronic symptom monitoring in a cohort of black and white bladder and prostate cancer patients. Qual Life Res. 2021 Nov;30(11):3213–27.
Samuel, Cleo A., et al. “Racial differences in user experiences and perceived value of electronic symptom monitoring in a cohort of black and white bladder and prostate cancer patients.Qual Life Res, vol. 30, no. 11, Nov. 2021, pp. 3213–27. Pubmed, doi:10.1007/s11136-020-02442-4.
Samuel CA, Smith AB, Elkins W, Richmond J, Mahbooba Z, Basch E, Bennett AV, Chung AE, Jonsson M, Chen RC, Reeve BB. Racial differences in user experiences and perceived value of electronic symptom monitoring in a cohort of black and white bladder and prostate cancer patients. Qual Life Res. 2021 Nov;30(11):3213–3227.
Journal cover image

Published In

Qual Life Res

DOI

EISSN

1573-2649

Publication Date

November 2021

Volume

30

Issue

11

Start / End Page

3213 / 3227

Location

Netherlands

Related Subject Headings

  • Urinary Bladder
  • Race Factors
  • Quality of Life
  • Prostatic Neoplasms
  • Patient Reported Outcome Measures
  • Male
  • Humans
  • Health Policy & Services
  • Electronics
  • 44 Human society