About this trial
SURGE aims to increase equity in clinical trial enrollment by addressing barriers to genomic testing, which is increasingly needed to assess precision clinical trial eligibility and access standard precision therapies. The study is an interventional pilot meant primarily to assess the feasibility of the intervention. The intervention is comprised of a patient navigator, text message questionnaire, and informational video.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adult (age 18 years or older)
Black, Latinx, OR older adult (age 70 years or older)
Scheduled for a new patient consultation
Suspected or confirmed advanced malignancy (requiring active treatment)
Disqualifiers
Malignancy or former malignancy that requires only surveillance
Not continuing care at a participating DFCI site
Speaks a language other than English or Spanish
Unable to provide consent
Trial design
Parallel
Treatments tested in this trial
SURGE
BehavioralVideo with or without person to person guidance to support decision making around genetic testing
Treatment groups
Trial outcomes
Primary outcomes
Genomic testing uptake
Intervention impact on rate of uptake of genomic testing
Secondary outcomes
Patient interaction with the intervention
Interaction with each component of the intervention (as appropriate by intervention arm)
Acceptability of questionnaire modality
We will use the System Usability Scale to measure usability of the questionnaire electronic tool. The 10-item System Usability Scale is scored on a five-point Likert scale, with 1 being Strongly Disagree and 5 being Strongly Agree.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Nadine McCleary, MD, MPH
Lead sponsor
Dana-Farber Cancer Institute
Sponsor institution
Bristol-Myers Squibb
Collaborator