Epidemiology Controls Using Healthy Participants

NCT ID: NCT00476632

Last Updated: 2019-05-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

1500 participants

Study Classification

OBSERVATIONAL

Study Start Date

2004-06-30

Study Completion Date

2019-06-30

Brief Summary

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The goal of this research study is to identify biologic and lifestyle factors that may increase a person's risk of developing certain types of cancer.

Detailed Description

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For this study, you will be asked to complete a personal interview. During the interview, you will be asked questions about your demographics (age, sex, etc.), certain environmental exposures, your medical history, family history, your diet, and your smoking and alcohol use histories. It should take around 50 minutes to complete the interview.

You will also have around 2 ½ tablespoons of blood drawn for special tests. These tests will look for any biologic factors associated with certain cancers. The interview and blood draw will be scheduled at the time and place of your convenience. You will not be informed of the results of any of the testing done with your samples.

There is a possibility that you might be contacted in the future about if researchers need clarification on any of information already collected. You are free to refuse any further participation if you wish.

This is an investigational study. Up to 1,500 participants will take part in this study.

Conditions

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Healthy

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Control

Person with no history of cancer.

Questionnaire

Intervention Type BEHAVIORAL

50 Minute Interview

Interventions

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Questionnaire

50 Minute Interview

Intervention Type BEHAVIORAL

Other Intervention Names

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Survey

Eligibility Criteria

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Inclusion Criteria

1. Individuals ages 18 and over with no prior cancer
2. Willing and able to complete an administered questionnaire
3. Willing and able to donate 30 mL of blood

Exclusion Criteria

1. Individuals with prior cancer
2. Individuals under the age of 18
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Cancer Institute (NCI)

NIH

Sponsor Role collaborator

National Institutes of Health (NIH)

NIH

Sponsor Role collaborator

M.D. Anderson Cancer Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Carrie Daniel-MacDougall, PHD

Role: PRINCIPAL_INVESTIGATOR

M.D. Anderson Cancer Center

Locations

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University of Texas MD Anderson Cancer Center

Houston, Texas, United States

Site Status

Countries

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United States

Related Links

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http://www.mdanderson.org

UT MD Anderson Cancer Center website

Other Identifiers

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P50CA100632

Identifier Type: NIH

Identifier Source: secondary_id

View Link

5R01CA070917-08

Identifier Type: NIH

Identifier Source: secondary_id

View Link

2004-0112

Identifier Type: -

Identifier Source: org_study_id

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