Actively Recruiting

Phase Not Applicable
Age: 21Years - 75Years
All Genders
ID05742178

NYC Cancer Outreach Network in Neighborhoods for Equity and Community Translation Randomized Controlled Trial (NYC CONNECT)

Led by NYU Langone Health · Updated on 2025-12-18

2160

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

Sponsors

N

NYU Langone Health

Lead Sponsor

C

Centers for Disease Control and Prevention

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are conducting a randomized controlled trial called NYC CONNECT to compare two strategies aimed at increasing cancer screening rates for breast, cervical, and colorectal cancers. The study focuses on individuals who are due for these cancer screenings and examines whether adding community health worker (CHW) navigation services to culturally and linguistically tailored cancer education improves screening rates compared to education alone. All participants will also receive support for social needs that may affect their health. Participants will be randomly assigned to one of two groups. The more intensive group receives patient navigation from trained, bilingual CHWs who provide support for cancer screening and social services alongside tailored educational materials. The less intensive group receives tailored educational materials and navigation for social service needs only. Both groups complete surveys at the start, 3 months, and 6 months. After 6 months, those in the less intensive group can opt to receive the full navigation support offered to the intensive group. Throughout the study, participants will complete surveys to assess their cancer screening status and social needs. Researchers will measure the percentage of participants who receive at least one cancer screening within 6 months of enrollment. The study includes ongoing support to address social determinants of health, and participation lasts at least 6 months with surveys conducted at regular intervals to monitor outcomes.

CONDITIONS

Brief Title

NYC Cancer Outreach Network in Neighborhoods for Equity and Community Translation

Who Can Participate

Age: 21Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Women between the ages of 21 and 75 years
  • Men between the ages of 45 and 75 years
  • Women aged 40-74 years who have not had a mammogram in the past 12 months, a Pap smear in the last 3 years (ages 21-64), or HPV test in the last 5 years (ages 30-64)
  • Women aged 45-75 years who are not up-to-date on colorectal cancer screening
  • Men not up-to-date on colorectal cancer screening
  • Must speak English, Spanish, Haitian-Creole, French, or Chinese (Mandarin or Cantonese)
  • Lives in East Flatbush, Sunset Park, Highbridge, or Morrisania zip codes
Not Eligible

You will not qualify if you...

  • Previous or current diagnosis of any cancer
  • Pregnancy (for breast and cervical cancer screening only)
  • Current participation in an existing cancer navigation program
  • Currently in hospice care
  • Age 66 or older with advanced illness or frailty or living in a long-term institution for more than 90 days
  • Bilateral mastectomy or both unilateral mastectomies (breast cancer only)
  • Hysterectomy with no residual cervix (cervical cancer only)
  • Total colectomy (colorectal cancer only)

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - 6 months

Participants receive patient navigation and tailored educational materials to support cancer screening and social service needs, based on their randomized group.

Surveys at baseline, 3 months, and 6 months

Trial Site Locations

Total: 2 locations

1

NYU Langone Health

New York, New York, United States, 10016

Actively Recruiting

2

Albert Einstein College of Medicine

The Bronx, New York, United States, 10461

Actively Recruiting

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Research Team

C

Chau Trinh-Shevrin, DrPH

P

Perla Chebli, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SCREENING

Number of Arms

2

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