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Assessing the Impact of Electronic Capture of Patient Reported Outcomes in Radiation Oncology

NCT02756767 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 75

Last updated 2021-06-07

No results posted yet for this study

Summary

The goals of this study are to assess the feasibility of weekly administration of site specific patient reported assessments using an electronic platform and to explore the correlation between patient reported outcomes as well as known dosimetric prognostic factors in patients with lung, breast, head and neck, or pelvic malignancies

Conditions

  • Patients With Lung, Breast, Head and Neck, or Pelvic Malignancies

Interventions

OTHER

Survey

Sponsors & Collaborators

  • Abramson Cancer Center at Penn Medicine

    lead OTHER

Principal Investigators

  • Lilie Lin, MD · Abramson Cancer Center at Penn Medicine

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-04-30
Primary Completion
2021-04-30
Completion
2021-04-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02756767 on ClinicalTrials.gov