NCT05948618
Improving PRO for Patients With Cancer Using ECAs and Data Visualization
Enrolling by Invitation
NAAges 18+InterventionalSupportive careTufts Medical CenterInvestigator-initiated
~100 participants
Updated 2026-03-04 on ClinicalTrials.gov
What's tested:Embodied Conversational AgentREDCap Survey
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
The degree of missing data will be investigated to gauge the extent to which patients are actively engaging with the ECA-PRO system.
Measured over 6 weeks
Conditions
Where it's being run
1 sites across 1 statesMassachusetts1
Study leadership
- Michael Paasche-Orlow, MD, MPH · PRINCIPAL_INVESTIGATOR · Tufts Medical Center
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
At least 18 years of age or older
Able to read and speak english
Can independently consent
Must have adequate corrected vision to use the ECA system (based on a 1 minute ECA functional screener)
Must have adequate hearing to use the ECA system.
Has a diagnosis of gastrointestinal cancer or head and neck cancer for which they are currently receiving chemotherapy and/or radiation treatment.
Provider subjects must be practicing oncologists at BMC.
Exclusion
If the subject is incarcerated
If the subject plans to leave the Boston area in the next 6 weeks
Is not able to use the ECA screener
What this trial measures
- The degree of missing data will be investigated to gauge the extent to which patients are actively engaging with the ECA-PRO system.6 weeks
Assessing the completeness of the Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) survey questions, taking into account the number of items that have been satisfactorily completed. By examining prevalence of missing data, the investigators aim to infer the level of patient utilization of the ECA-PRO system.