Actively Recruiting

Age: 30Years - 70Years
All Genders
Healthy Volunteers
NCT04609072

Connect for Cancer Prevention Study (Connect)

Led by National Cancer Institute (NCI) · Updated on 2026-05-08

200000

Participants Needed

10

Research Sites

2579 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Background: The National Cancer Institute, part of the National Institutes of Health, has partnered with nine health care systems across the U.S. to establish the Connect for Cancer Prevention Study. While researchers have made important discoveries, there is more to learn to lower the number of people affected by cancer. By taking part in Connect, participants can help researchers learn how the way we live, our genetics, and our health history may affect cancer risk. Objective: To study and better understand the causes of cancer and to find new ways to prevent it. Eligibility: The study will include 200,000 adults who get their health care from a partner health care system, are between 30 and 70 years old at enrollment, and have never had cancer. People remain eligible to join if they have or once had non-melanoma skin cancer, or a condition that may raise cancer risk (such as ductal carcinoma in situ, or DCIS). Design: Eligible recruits can sign up for Connect online by creating an account on MyConnect using their email address or phone number. After creating an account, they will complete the informed consent process. All information shared through MyConnect is secure to protect participant privacy. After joining the study, participants will be asked to answer online health surveys a few times a year, donate samples of blood, urine, and saliva every two to three years, and safely share access to their electronic health records with Connect. In the future, participants may donate unused samples that are collected at clinical visits, like tissue, stool, or blood, and may mail in samples collected at home. Participants may also share information from personal health trackers, like wearable devices or apps. This information will help researchers study the health and behavior patterns that may affect cancer risk. It takes time to understand the causes of cancer, so Connect will go on for many years. The longer people participate, the more researchers may learn. Participants can leave the study at any time. Learn more about Connect by visiting cancer.gov/connectstudy.

CONDITIONS

Official Title

Connect for Cancer Prevention Study (Connect)

Who Can Participate

Age: 30Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients or members of participating integrated health care systems at the time of enrollment
  • Age between 30 and 70 years old at study invitation
Not Eligible

You will not qualify if you...

  • Individuals with a confirmed history of invasive cancer (other than non-melanoma skin cancer)
  • Individuals with known cognitive impairment documented in their medical record

AI-Screening

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Trial Site Locations

Total: 10 locations

1

Kaiser Permanente Colorado

Denver, Colorado, United States, 80247

Actively Recruiting

2

Kaiser Permanente Georgia

Atlanta, Georgia, United States, 30305

Actively Recruiting

3

Kaiser Permanente Hawaii

Honolulu, Hawaii, United States, 96814

Actively Recruiting

4

University of Chicago Medical Center

Chicago, Illinois, United States, 60603

Active, Not Recruiting

5

Henry Ford Health Systems

Detroit, Michigan, United States, 48202

Actively Recruiting

6

HealthPartners

Minneapolis, Minnesota, United States, 55425

Actively Recruiting

7

Kaiser Permanente Northwest

Portland, Oregon, United States, 97086

Actively Recruiting

8

Sanford Health

Sioux Falls, South Dakota, United States, 57117

Actively Recruiting

9

Baylor Scott and White Health

Dallas, Texas, United States, 75246

Actively Recruiting

10

Marshfield Clinic Health System

Marshfield, Wisconsin, United States, 54449

Actively Recruiting

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Research Team

N

Nicolas A Wentzensen, M.D.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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