New study tests whether a navigator can close gaps in breast cancer care
NCT ID NCT06350500
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is testing a patient navigation program for women newly diagnosed with breast cancer. The program helps patients understand their care options, connect to support services, and manage barriers like transportation or finances. Researchers want to see if this approach improves health equity and quality of life.
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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About 126 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2024
- Expected to finish
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Mar 2028
An estimate. End dates often move.
- 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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Female participants only
- 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age ≥ 18 years of age * Have a confirmed diagnosis of breast cancer or Ductal Carcinoma In Situ (DCIS) * Currently identify their gender as woman or female * Was assigned female sex at birth (AFAB) \- Participant is experiencing ≥1 barrier to care as determined by the social needs screening tool * Participant must understand the investigational nature of this study and verbally consent to participate prior to receiving any study related intervention Exclusion Criteria: * Participants who are not suspected of or diagnosed with breast cancer or Ductal Carcinoma in Situ (DCIS) * Participants who have had a previous diagnosis of any cancer * Participants who were assigned male sex or intersex at birth * Unwilling or unable to follow protocol requirements
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Roswell Park Comprehensive Cancer Center
RECRUITINGBuffalo, New York, 14263, United States
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