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Evaluating Patient Reported Outcomes in Radiation Therapy, The PRO-RT Study

Breast Carcinoma Clinical Trial

Official title:
Patient Reported Outcomes in Radiation Therapy (PRO-RT)

Clinical Trial Summary

This study explores the use of the Hugo platform to involve study participants in their healthcare and treatments. The Hugo platform may allow researchers to collect better and more accurate real-time health data, from other clinics/hospitals, pharmacies and other electronic devices. The purpose of this research is to see if the use of the Hugo platform is consistent, accurate, cost effective, and time efficient, as it collects and transmits important real-time health information from other clinics/hospitals, pharmacies, and other electronic devices.

Clinical Trial Description

PRIMARY OBJECTIVES: I. Evaluate the data aggregation from a patient centered platform over a follow up period for completeness and quality, including externally linked electronic health record (EHR) information, toxicity completion, and the patient reported outcomes (PRO) response rates for study patients, compared with historical pre-coronavirus disease (COVID) cohort of registry patients. II. To explore biometric information obtained from wearables as it pertains to the toxicity of treatment for patients using a wearable device. III. To estimate app-based survey completion rates using Hugo-based survey incentive completion (gift cards). IV. To explore the cost data available on the platform. OUTLINE: Patients complete surveys via the Hugo Platform at baseline (before treatment), after treatment, and at 3 and 6 months after treatment. Patients' medical records and Fitbit information are also collected into the Hugo Platform. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05224271
Study type Observational
Source Mayo Clinic
Contact
Status Active, not recruiting
Phase
Start date March 2, 2022
Completion date December 30, 2024
View Details
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