A Study of a Side Effects and Resource Navigation Program for People With Cancer

This study is looking at an Immunotherapy CARE Program to see if it helps people with kidney, bladder, breast, or lung cancer manage their immunotherapy treatment better. The program involves staff helping with essential needs and reporting side effects. You might be able to join if you are 18 or older, have one of these cancers, and are starting treatment with PD-1 or PD(L)-1 immune checkpoint inhibitors. The study will measure if participants continue their immunotherapy treatment for at least 6 months and will also look at how the program affects your quality of life through questionnaires. The study is currently unclear on its recruitment status and plans to enroll 200 people.

Study design
This is an interventional study with an unclear status, planning to enroll 200 participants.
What's involved
If assigned to the I CARE arm, CCNY staff will assist you monthly with essential needs and side effects/symptom reporting. You will also complete questionnaires to measure your quality of life.
Compensation
Not stated in the trial record.
Follow-up
The study measures immunotherapy continuation at 6 months, suggesting follow-up for at least that long.

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NCT07646847

A Study of a Side Effects and Resource Navigation Program for People With Cancer

Recruiting
NAAges 18+InterventionalDiagnostic
Memorial Sloan Kettering Cancer Center
~200 participants
Updated 2026-07-31 on ClinicalTrials.gov
What's tested:Immunotherapy CARE Program

At a glance

Recruiting sites
7 of 8 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Immune Checkpoint Inhibitors/ICI continuation
Measured over 6 months
Kidney Cancer
Bladder Cancer
Breast Cancer
Lung Cancer
8 sites across 2 states
New York5
New Jersey3
  • Francesca Gany, MD, MS · PRINCIPAL_INVESTIGATOR · Memorial Sloan Kettering Cancer Center

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

Documentation of Disease
Prior Treatment
Age ≥ 18 (per EMR)
Not Pregnant and Not Nursing (per self-report)
At least one essential need (e.g., food, transportation, housing), as determined by the ICCAN Essential Needs Screener (per self-report)
Lives in New York metro area, including Long Island, New Jersey, Connecticut, and Pennsylvania (per self-report)
Can speak English or Spanish (per self-report)
Has no significant psychiatric disturbance sufficient to preclude completion of the assessment measures, interview, or informed consent (i.e., acute psychiatric symptoms which require individual treatment) (per EMR, patient's care team, or study team)
Has no presence of cognitive impairment disorder (i.e., delirium or dementia) sufficient to preclude meaningful informed consent and/or data collection (per EMR, patient's care team, or study team)
  • Immune Checkpoint Inhibitors/ICI continuation6 months

    Participant ICI appointment and treatment adherence will be documented through chart abstraction (research staff EMR review) at 6 months