A Study of a Distress Screening and Referral Program in People With Recently Diagnosed Cancer
NCT ID: NCT07117461
Last Updated: 2025-10-16
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
NA
50 participants
INTERVENTIONAL
2025-07-22
2026-07-22
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Participants with a New Solid Tumor Diagnosis
Participants will have a new solid tumor cancer diagnosis.
NCCN Distress Thermometer
A tool used to determine on a number scale the amount of distress for the past week
Interventions
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NCCN Distress Thermometer
A tool used to determine on a number scale the amount of distress for the past week
Eligibility Criteria
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Inclusion Criteria
* Treated or will be treated at Jamaica Hospital Medical Center (per EMR)
* Has a NCCN DT score of 0 through 10 (per EMR)
* Age ≥ 18 years (per EMR or self-report)
* English- or Spanish preferred language for healthcare (per self-report)
* Able to provide consent (per completion of consent)
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Memorial Sloan Kettering Cancer Center
OTHER
Responsible Party
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Principal Investigators
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Devika Jutagir, PhD
Role: PRINCIPAL_INVESTIGATOR
Memorial Sloan Kettering Cancer Center
Locations
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Memorial Sloan Kettering Cancer Center (All Protocol Activities)
New York, New York, United States
Medisys Health Network (Data Collection Only)
Richmond Hill, New York, United States
Countries
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Central Contacts
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Facility Contacts
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Devika Jutagir, PhD
Role: primary
Ateaya Lima, MD
Role: primary
Related Links
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Memorial Sloan Kettering Cancer Center
Other Identifiers
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24-296
Identifier Type: -
Identifier Source: org_study_id
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