Electronic Patient Reported Outcomes in Patients With Gastrointestinal Cancers
Launched by UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · Apr 27, 2022
Trial Information
Current as of April 24, 2025
Withdrawn
Keywords
ClinConnect Summary
PRIMARY OBJECTIVES:
I. To evaluate the feasibility of the ePRO platform by describing the proportion of participants who engage with the ePRO tool via virtual care chat at least once after enrollment.
II. To investigate the potential differences in health-related quality of life (HRQoL) by comparing the change in overall score of EuroQol five-dimensional Questionnaire (EQ-5D) index.
SECONDARY OBJECTIVES:
I. To evaluate the degree of engagement with virtual care chat as defined by the proportion of chat modules completed.
II. To measure the potential differences in health-related qualit...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Age 18 years and older
- • Diagnosis of gastrointestinal cancers: esophageal, gastric, hepatocellular carcinoma, cholangiocarcinoma, pancreatic, neuroendocrine, small intestine, colorectal and anal cancers.
- • Patients can have early stage or advanced cancer and will be starting treatment with new, standard of care infusion therapy regimen at UCSF.
- • Ability to understand study procedures and to comply with them for the entire length of the study.
- • No limit on prior lines of therapy.
- • Access to smartphone, tablet, or computer with capability to use symptom tracking web site (must have mobile phone number or email address).
- • Willing and able to provide written, signed informed consent in English.
- • Ability of individual or legal guardian/representative to understand a written informed consent document, and the willingness to sign it.
- Exclusion Criteria:
- • Patients who have already started therapy prior to study enrollment.
- • Patients who are receiving their treatment outside of UCSF.
- • Participation in another clinical trial (therapeutic or non-therapeutic).
- • Patients who are on therapy with oral oncolytics or combination therapy of oral oncolytics and infusional agents.
- • Patients who are non-English speakers.
Trial Officials
Wesley A Kidder, MD
Principal Investigator
University of California, San Francisco
About University Of California, San Francisco
The University of California, San Francisco (UCSF) is a leading academic institution renowned for its commitment to advancing healthcare through innovative research and clinical trials. With a focus on translating scientific discoveries into effective therapies, UCSF collaborates with a diverse array of stakeholders, including healthcare professionals, industry partners, and patient communities. The university's research programs emphasize interdisciplinary approaches and leverage cutting-edge technology to address complex medical challenges. As a sponsor of clinical trials, UCSF is dedicated to maintaining the highest standards of ethical conduct and scientific rigor, ensuring the safety and well-being of participants while contributing to the broader medical knowledge base.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
San Francisco, California, United States
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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