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.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
A Study of a Side Effects and Resource Navigation Program for People With Cancer
At a glance
Conditions
NCT07646847
Where you'd take part
This study runs at 8 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
City College of New York (Data Collection AND Specimen Analysis)
New York, New Yorkstudy coordinator listed
Not yet recruiting
Memorial Sloan Kettering Basking Ridge (All Protocol Activities)
Basking Ridge, New Jerseystudy coordinator listed
Recruiting
Memorial Sloan Kettering Bergen (All Protocol Activities)
Montvale, New Jerseystudy coordinator listed
Recruiting
Memorial Sloan Kettering Cancer Center (All Protocol Activities)
New York, New Yorkstudy coordinator listed
Recruiting
Memorial Sloan Kettering Monmouth (All Protocol Activities)
Middletown, New Jerseystudy coordinator listed
Recruiting
Memorial Sloan Kettering Nassau (All protocol activities)
Rockville Centre, New Yorkstudy coordinator listed
Recruiting
Memorial Sloan Kettering Suffolk- Commack (All Protocol Activities)
Commack, New Yorkstudy coordinator listed
Recruiting
Memorial Sloan Kettering Westchester (All Protocol Activities)
Harrison, New Yorkstudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Francesca Gany, MD, MS · PRINCIPAL_INVESTIGATOR · Memorial Sloan Kettering Cancer Center
Who to contact
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Inclusion
What this trial measures
- 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