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Spots Global Cancer Trial Database for Digital Symptom Tracking, Patient Engagement and Quality of Life in GI Oncology Clinic Patients

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Digital Symptom Tracking, Patient Engagement and Quality of Life in GI Oncology Clinic Patients

Official Title: Feasibility Study of Digital Symptom Tracking, Patient Engagement and Quality of Life in Patients Seen in GI Oncology Clinic

Study ID: NCT03459352

Conditions

Cancer

Interventions

ePRO

Study Description

Brief Summary: A pilot study of an ePRO system in cancer patients receiving systemic therapies.

Detailed Description: The primary purpose of this pilot study is to determine the feasibility of the Noona Healthcare Mobile PRO Application to describe oncology patient engagement using a web-based symptom self-monitoring instrument. Additionally, the studyy will dentify side effects as well as long term or chronic adverse events during and following cancer therapy based on the United States (US) National Cancer Institute (NCI) Patient Reported Outcomes Common Terminology Criteria for Adverse Events (PRO-CTCAE), and identify patients to participate in future long-term Quality of Life studies following cancer therapy. The study is not intended to compare outcomes between groups receiving different therapies.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Duke University Medical Center, Durham, North Carolina, United States

Contact Details

Name: H. Kim Lyerly, MD

Affiliation: Duke University

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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