Fact CheckerSign in

NCT07646847Recruiting

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

I CARE (Immunotherapy Cutaneous Adverse Events REsearch) - A Trial With Diverse Cancer Patients to Determine the Impact of SDoH and Side Effects Navigation Program on Treatment Continuation

Source: ClinicalTrials.gov · Last updated 28 Oct 2026

Brief summary (registry, in English)

The purpose of this study is to find out if the navigation program helps participants manage immunotherapy treatment better than usual care. Investigators will also look at how the navigation program impacts participants' quality of life. Investigators will measure quality of life by having participants complete questionnaires.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
200 (estimated)
First submitted
9 Jun 2026
Start date
Jun 2026
Primary completion date
Jun 2029
Lead sponsor
Memorial Sloan Kettering Cancer Center
NCT number
NCT07646847

What you commit to

  • Study type: Interventional
  • Planned participants: 200
  • From Jun 2026 to the primary completion date, Jun 2029
  • 8 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Who the study is looking for

  • Documentation of Disease
    • o Patient must have pathologically confirmed kidney, bladder, breast, gastrointestinal or lung cancer (per EMR)
  • Prior Treatment
    • o Within three weeks (+/- 3 weeks) of starting PD-1 or PD(L)-1 immune checkpoint inhibitors as monotherapy or in combination with other therapies (per EMR)
  • 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)
  • Screens positive on SDOH screening tool, referred by the clinical team through traditional screening tools for SDOH assistance orand demonstrates financial need per MSK guidelines (up to 500% of the federal poverty limit) (per EMR or 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 serious life-threatening allergies to tape or adhesives (per EMR or 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)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (8)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Memorial Sloan Kettering Basking Ridge (All Protocol Activities)
Coordinator of this site? Confirm its status
Basking RidgeUnited StatesRecruiting
Memorial Sloan Kettering Suffolk - Commack (All Protocol Activities)
Coordinator of this site? Confirm its status
CommackUnited StatesRecruiting
Memorial Sloan Kettering Westchester (All Protocol Activities)
Coordinator of this site? Confirm its status
HarrisonUnited StatesRecruiting
Memorial Sloan Kettering Monmouth (All Protocol Activities)
Coordinator of this site? Confirm its status
MiddletownUnited StatesRecruiting
Memorial Sloan Kettering Bergen (All Protocol Activities)
Coordinator of this site? Confirm its status
MontvaleUnited StatesRecruiting
City College of New York (Data Collection AND Specimen Analysis)
Coordinator of this site? Confirm its status
New YorkUnited StatesNot yet recruiting
Memorial Sloan Kettering Cancer Center (All Protocol Activities)
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting
Memorial Sloan Kettering Nassau (All Protocol Activities)
Coordinator of this site? Confirm its status
Rockville CentreUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.