No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
35 and older
Sex
Any
Study type
Observational
Participants needed
100,000 (estimated)
Sponsor
National Minority Quality Forum · Other
Who this trial is looking for
This trial is looking for adults aged 35 and older to help research cancer care and barriers to screening in underrepresented communities. Participants will attend annual clinic visits, answer health questionnaires, allow access to their medical records, and provide some samples for research.
Are You a Good Fit for This Trial?
You may be able to join if
I am 35 years or older.
I can give written informed consent.
I understand the purpose of the study.
I agree to share my health information for research.
I agree to allow access to my medical records.
I can participate for the full duration of the study.
I am healthy and a nonpregnant adult.
You may not be able to join if
I cannot give written informed consent.
I am under 35 years old.
I think I may be pregnant or planning to get pregnant.
I weigh less than 110 pounds.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
The goal of this observational study is to establish a patient registry and a biorepository (sample collection and storage) to investigate health disparities, access, and barriers to cancer screening and early detection technologies. The registry and biorepository will serve as a resource to support Cancer Early Detection (CED) screenings and future research focused on communities at increased ris…
The goal of this observational study is to establish a patient registry and a biorepository (sample collection and storage) to investigate health disparities, access, and barriers to cancer screening and early detection technologies. The registry and biorepository will serve as a resource to support Cancer Early Detection (CED) screenings and future research focused on communities at increased risk for cancer.
The study seeks to address:
•Barriers and disparities in cancer prevention, screening, and treatment, particularly in historically underrepresented populations.
Participants will:
* Attend a minimum of five clinic visits over a five-year period for scheduled annual assessments while actively enrolled in the study.
* Complete questionnaires at each visit that collect information on their medical history, cancer history, and family cancer history.
* Allow relevant health information from their electronic health records (EHR) to be collected and reviewed.
* Provide blood, saliva, and stool samples for research purposes.
* Enter a long-term follow-up period for an additional five years.
Trial Locations
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Facility
City
State
Country
Status
Eligibility Criteria
Registry
Inclusion Criteria:
1. Adults 35 years and older.
2. Participant provides written informed consent prior to initiation of any study procedures.
3. Participant understands the purpose and procedures of the study.
4. Participant agrees that demographic data, medical history, and social dete…
Registry
Inclusion Criteria:
1. Adults 35 years and older.
2. Participant provides written informed consent prior to initiation of any study procedures.
3. Participant understands the purpose and procedures of the study.
4. Participant agrees that demographic data, medical history, and social determinants of health on the enrollment questionnaires can be used for research purposes.
5. Participant agrees to the release and review of their electronic medical record.
6. Participant agrees to be followed for the duration outlined in this protocol.
Biorepository
1. Participant is able, in the investigator's professional opinion, to provide up to 100 mLs of whole blood at the Screening Visit and at the Interim Visits.
2. Participant is a healthy, nonpregnant adult.
3. Participant weighs at least 110 pounds.
4. Participant has negative viral test results.
Exclusion Criteria:
Registry
1. Any medical or mental condition that would interfere with the subjects' ability to willingly give written informed consent.
2. Participants who are unable to understand the study protocol or unable to give informed consent.
3. Participants under the age of 35 at the time of enrollment.
Biorepository
1. Women of childbearing age that think they may be pregnant or are planning to get pregnant within the study timeframe.
2. Participants who weigh under 110 pounds.
3. Participants who, in the opinion of the investigator, are unable to provide biospecimen samples.
Contacts
No contact information available.
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