Remote Patient-Reported Outcomes and Activity Monitoring to Improve Patient-Clinician Communication Regarding Symptoms and Functional Status: A Randomized Controlled Trial

Author:

Parikh Ravi B.1234ORCID,Schriver Emily56ORCID,Ferrell William J.23ORCID,Wakim Jonathan3,Williamson Joelle3,Khan Neda237,Kopinsky Michael7ORCID,Balachandran Mohan7,Gabriel Peter E.1ORCID,Schuchter Lynn M.1,Patel Mitesh S.8,Shulman Lawrence N.1ORCID,Manz Christopher R.910ORCID

Affiliation:

1. Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA

2. Leonard Davis Institute for Health Economics, University of Pennsylvania, Philadelphia, PA

3. Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA

4. Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA

5. Institute for Biomedical Informatics, University of Pennsylvania, Philadelphia, PA

6. Penn Medicine Predictive Healthcare, University of Pennsylvania Health System, Philadelphia, PA

7. Center for Health Care Innovation, Penn Medicine, Philadelphia, PA

8. Ascension, St Louis, MO

9. Division of Population Sciences, Dana-Farber Cancer Institute, Boston, MA

10. Harvard Medical School, Harvard University, Boston, MA

Abstract

PURPOSE Routine collection of patient-generated health data (PGHD) may promote earlier recognition of symptomatic and functional decline. This trial assessed the impact of an intervention integrating remote PGHD collection with patient nudges on symptom and functional status understanding between patients with advanced cancer and their oncology team. METHODS This three-arm randomized controlled trial was conducted from November 19, 2020, to December 17, 2021, at a large tertiary oncology practice. We enrolled patients with stage IV GI and lung cancers undergoing chemotherapy. Over 6 months, patients in two intervention arms received PROStep—weekly text message–based symptom surveys and passive activity monitoring using a wearable accelerometer. PGHD were summarized in dashboards given to patients' oncology team before appointments. One intervention arm received an additional text-based active choice prompt to discuss worsening symptoms or functional status with their clinician. Control patients did not receive PROStep. The coprimary outcomes patient perceptions of oncology team symptom and functional understanding at 6 months were measured on a 1-5 Likert scale (5 = high understanding). RESULTS One hundred eight patients enrolled: 55% male, 81% White, and 77% had GI cancers. Patient-reported clinician understanding did not differ between control and intervention arms for symptoms (4.5 v 4.5; P = .87) or functional status (4.5 v 4.3; P = .31). In the intervention arms, combined patient adherence to weekly symptom reports and daily activity monitoring was 64% and 53%, respectively. Intervention patients in the PROStep versus PROStep + active choice arms reported low burden from wearing the accelerometer (mean burden [standard deviation], 2.7 [1.3] v 2.1 [1.3]; P = .15) and completing surveys (2.1 [1.2] v 1.9 [1.3]; P = .44). CONCLUSION Patients receiving PROStep reported high understanding of symptoms and functional status from their oncology team, although this did not differ from controls.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Oncology (nursing),Health Policy,Oncology

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