Assessing Patient Perspectives and the Health Equity of a Digital Cancer Symptom Remote Monitoring and Management System

Author:

Mooney Kathi12ORCID,Beck Susan L.12,Wilson Christina3ORCID,Coombs Lorinda4ORCID,Whisenant Meagan5ORCID,Moraitis Ann Marie6,Sloss Elizabeth A.1ORCID,Alekhina Natalya1ORCID,Lloyd Jennifer12ORCID,Steinbach Mary12ORCID,Nicholson Bridget1,Iacob Eli1,Donaldson Gary17

Affiliation:

1. College of Nursing, University of Utah, Salt Lake City, UT

2. Huntsman Cancer Institute, University of Utah, Salt Lake City, UT

3. School of Nursing, University of Alabama at Birmingham, Birmingham, AL

4. School of Nursing, University of North Carolina at Chapel Hill, Chapel Hill, NC

5. Department of Behavioral Science, University of Texas MD Anderson Cancer Center, Houston, TX

6. Department of Pediatric Oncology, Dana Farber Cancer Institute, Boston, MA

7. School of Medicine, University of Utah, Salt Lake City, UT

Abstract

PURPOSE People with cancer experience poorly controlled symptoms that persist between treatment visits. Automated digital technology can remotely monitor and facilitate symptom management at home. Essential to digital interventions is patient engagement, user satisfaction, and intervention benefits that are distributed across patient populations so as not to perpetuate inequities. We evaluated Symptom Care at Home (SCH), an automated digital platform, to determine patient engagement, satisfaction, and whether intervention subgroups gained similar symptom reduction benefits. METHODS 358 patients with cancer receiving a course of chemotherapy were randomly assigned to SCH or usual care (UC). Both groups reported daily on 11 symptoms and completed the SF36 (Short Form Health Survey) monthly. SCH participants received immediate automated self-care coaching on reported symptoms. As needed, nurse practitioners followed up for poorly controlled symptoms. RESULTS The average participant was White (83%), female (75%), and urban-dwelling (78.6%). Daily call adherence was 90% of expected days. Participants reported high user satisfaction. SCH participants had lower symptom burden than UC in all subgroups: age, sex, race, income, residence type, diagnosis, and stage (all P < .001 effect size 0.33-0.65), except for stages I and II cancers. Non-White and lower-income SCH participants gained a higher magnitude of symptom reduction than White participants and higher-income participants. Additionally, SCH men gained higher SF36 mental health (MH) benefit. There were no differences on other SF36 indices. CONCLUSION Participants were highly satisfied and consistently engaged the SCH platform. SCH men gained large MH improvements, perhaps from increased comfort in sharing concerns through automated interactions. Although all intervention subgroups benefited, non-White participants and those with lower income gained higher symptom reduction benefit, suggesting that systematic care through digital tools can overcome existing disparities in symptom care outcomes.

Publisher

American Society of Clinical Oncology (ASCO)

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