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Clinical trialNCT03850912CompletedInterventional

Symptom Management Implementation of Patient Reported Outcomes in Oncology

SponsorDana-Farber Cancer InstituteEnrollment42,808Gastrointestinal CancerGynecologic CancerOther CancerThoracic Cancer
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

Deficits in the management of common symptoms cause substantial morbidity for cancer patients.Because the health care delivery system is structured to be reactive and not proactive, there are missed opportunities to optimize symptom control. Growth in Internet access and proliferation of smartphones has created an opportunity to re-engineer cancer care delivery. Electronic symptom tracking and feedback is a promising strategy to improve symptom control. Electronic patient reported outcome (ePRO) monitoring of cancer symptoms has been shown to decrease symptom burden, improve quality of life, reduce acute care and even extend survival. SIMPRO will use functioning ePRO prototypes to create and refine the electronic symptom management system eSyM

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

6 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Maine Medical Center

    Portland, Maine, United States

  • Dana Farber Cancer Institute

    Boston, Massachusetts, United States

  • Dartmouth-Hitchcock Medical Center

    Lebanon, New Hampshire, United States

  • Brown University Health (formerly Lifespan Cancer Institute)

    Providence, Rhode Island, United States

  • Baptist Memoiral Healthcare

    Memphis, Tennessee, United States

  • West Virginia University Medical Center

    Morgantown, West Virginia, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
25 Jul 2019
Primary completion
31 Mar 2023
Completion
9 Jun 2025
Last update posted
27 Aug 2025
Registered enrollment
42,808
Registry id
NCT03850912

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.