Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07117461

A Study of a Distress Screening and Referral Program in People With Recently Diagnosed Cancer

Led by Memorial Sloan Kettering Cancer Center · Updated on 2025-10-16

50

Participants Needed

2

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

It is recommended that cancer centers screen patients for distress and refer them to mental health services when their distress levels reach a certain level. However, many cancer centers don't have distress screening and referral programs. This study will provide valuable information about one distress screening and referral program and whether it can be helpful for a large and diverse group of cancer patients that includes both English- and Spanish-speaking patients.

CONDITIONS

Official Title

A Study of a Distress Screening and Referral Program in People With Recently Diagnosed Cancer

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • New solid tumor cancer diagnosis (per EMR)
  • Treated or will be treated at Jamaica Hospital Medical Center (per EMR)
  • Has a NCCN DT score of 0 through 10 (per EMR)
  • Age �3e�3d 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)
Not Eligible

You will not qualify if you...

  • Cognitively not intact to participate in the study as judged by provider or investigative team (per EMR or investigative team)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Memorial Sloan Kettering Cancer Center (All Protocol Activities)

New York, New York, United States, 10065

Actively Recruiting

2

Medisys Health Network (Data Collection Only)

Richmond Hill, New York, United States, 11418

Actively Recruiting

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Research Team

D

Devika Jutagir, PhD

CONTACT

F

Francesca Gany, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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