Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
5000 participants
OBSERVATIONAL
2025-11-24
2030-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Study Groups
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Observational
Patients complete a survey and have their medical records reviewed on study. Patients who score a 7 or higher on the NCCN distress thermometer receive distress management patient education materials and recommendation to follow up with their care team.
Non-Interventional Study
Non-interventional study
Interventions
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Non-Interventional Study
Non-interventional study
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Must have a diagnosis of neoplasm
* Must be actively undergoing radiation therapy (RT) or have completed RT within the last month at Mayo Clinic in Rochester
* Able to read and write in English
* Must have email and Mayo Clinic patient portal access
Exclusion Criteria
* Patients who have been seen in consultation but not recommended for radiation
18 Years
ALL
No
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Principal Investigators
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May Elbanna, MB, BCh, PhD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic in Rochester
Rochester, Minnesota, United States
Countries
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Central Contacts
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Facility Contacts
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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NCI-2025-09164
Identifier Type: REGISTRY
Identifier Source: secondary_id
24-011548
Identifier Type: OTHER
Identifier Source: secondary_id
ROR2503
Identifier Type: -
Identifier Source: org_study_id
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