New dashboard aims to make leukemia trials more inclusive
NCT ID NCT06795139
First seen Jul 16, 2026 · Last updated Jul 17, 2026 · Updated 1 time
Summary
This study tests a data visualization tool called the Trial Enrollment Diversity Dashboard (TEDD) designed to help doctors see how diverse their clinical trial enrollments are. The goal is to overcome racial and ethnic disparities in leukemia trial participation. The study enrolls healthcare professionals who treat leukemia patients and measures how often they use the dashboard over four three-month periods.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Trial Enrollment Diversity Dashboard (TEDD) behavioral intervention
- What this could lead to
- If successful, this dashboard could help make clinical trials more representative of the diverse populations they aim to serve.
- What could go wrong
- This is a small feasibility pilot with only 12 participants, so results may not apply broadly. The tool's impact on actual diversity is not yet measured.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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12 people
The number who actually took part.
- Started
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Mar 2025
- Finished
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May 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria Medical Professionals: * Physician, nurse practitioner, or physician assistant -≥10% clinical effort (or one ½ day of clinic per week for those working \<1 FTE) * Treats adult patients with leukemia or related diseases at the study sites * Ability to understand and willingness to provide informed consent * Age 18 or older Inclusion Criteria Participant Population: * Age ≥18 years old * Diagnosis of leukemia, lymphoma, myeloma, or related diseases * Seen by a physician for this diagnosis at one of the study sites Exclusion Criteria Medical Professionals: -Listed member of the research team Exclusion Criteria Participant Population: -Participants without the diagnoses of interest listed above, participants not seen at the study sites.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Dana-Farber Cancer Institute
Boston, Massachusetts, 02215, United States
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Other studies related to the condition(s) this trial covers.
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