SURGE: Supporting UnderRepresented Minorities in Genomics-based Cancer Trial Enrollment (Intervention)

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorNadine McCleary, MD, MPH

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • SURGE

    Behavioral

    Video with or without person to person guidance to support decision making around genetic testing

Treatment groups

210 Participants
are divided into 3 treatment groups
Group A: Arm B (informational video)Experimental treatment 1 intervention
Group B: Arm A (standard of care)No intervention 0 interventions
Group C: Arm C (informational video and patient navigation)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Genomic testing uptake

Intervention impact on rate of uptake of genomic testing

Time frame
Up to 90 days of enrollment

Secondary outcomes

1

Patient interaction with the intervention

Interaction with each component of the intervention (as appropriate by intervention arm)

Time frame
Up to 30 days of enrollment
2

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.

Time frame
Up to 30 days of enrollment

Other outcomes

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