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Recruiting NCT06469307

NCT06469307 Driving Inclusivity, Validity, and Equity in Research Through Strategic Engagement (DIVERSE)

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Clinical Trial Summary
NCT ID NCT06469307
Status Recruiting
Phase
Sponsor Dana-Farber Cancer Institute
Condition Blood Cancer
Study Type INTERVENTIONAL
Enrollment 40 participants
Start Date 2024-12-09
Primary Completion 2026-07-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
DIVERSE Review Process

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 40 participants in total. It began in 2024-12-09 with a primary completion date of 2026-07-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The purpose of this research study is to enhance inclusion and diversity in clinical trial enrollment by training participants to perform and provide feedback through a community-based protocol review process, called DIVERSE.

Eligibility Criteria

CAB Participant Inclusion Criteria: * Age 18 or older * English speaking * Ability to understand and willingness to provide oral consent * DFCI patient who are in remission from a blood cancer \>1 year will be preferred. CAB Participant Exclusion Criteria: * Adults unable to consent * Individuals who are not yet adults (infants, children, teenagers \<18 years old) * Prisoners. * Unwilling/unable to agree to maintaining the confidentiality of reviews and clinical trial materials, as outlined in Section 9.1 * Note 1: Patients and non-patient community members who are pregnant are eligible. This is a non-interventional study that meets the definition of minimal risk and poses no greater risk to pregnant individuals or fetuses. Pregnancy status will not be assessed. * Note 2: English fluency is necessary as protocols being reviewed are written in English and cannot be feasibly translated to other languages within the time period necessary to complete timely reviews. Investigator Participant Inclusion Criteria: * Age 18 older * English Speaking * Site or Principal investigator * Not a member of the research team

Contact & Investigator

Central Contact

Andrew Hantel, MD

✉ Andrew_Hantel@dfci.harvard.edu

📞 617-582-9394

Principal Investigator

Andrew Hantel, MD

PRINCIPAL INVESTIGATOR

Dana-Farber Cancer Institute

Frequently Asked Questions

Who can join the NCT06469307 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Blood Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06469307 currently recruiting?

Yes, NCT06469307 is actively recruiting participants. Contact the research team at Andrew_Hantel@dfci.harvard.edu for enrollment information.

Where is the NCT06469307 trial being conducted?

This trial is being conducted at Boston, United States.

Who is sponsoring the NCT06469307 clinical trial?

NCT06469307 is sponsored by Dana-Farber Cancer Institute. The principal investigator is Andrew Hantel, MD at Dana-Farber Cancer Institute. The trial plans to enroll 40 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology