Clincosm LogoSign in Get a demo

Epidemiology Controls Using Healthy Participants

Sponsor
M.D. Anderson Cancer Center (Other)
Overall Status
Unknown status
CT.gov ID
NCT00476632
Collaborator
National Cancer Institute (NCI) (NIH), National Institutes of Health (NIH) (NIH)
1,500
Enrollment
1
Location
180
Anticipated Duration (Months)
8.3
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Questionnaire

Detailed Description

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.

Study Design

Study Type:
Observational
Anticipated Enrollment :
1500 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Epidemiology Controls Using Healthy Participants
Actual Study Start Date :
Jun 1, 2004
Anticipated Primary Completion Date :
Jun 1, 2019
Anticipated Study Completion Date :
Jun 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Control

Person with no history of cancer.

Behavioral: Questionnaire
50 Minute Interview
Other Names:
  • Survey

    		•

    Outcome Measures

    Primary Outcome Measures

    1. To identify biologic and lifestyle factors that may increase a person's risk of developing certain types of cancer. [6 Years]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Texas MD Anderson Cancer Center Houston Texas United States 77030

    Sponsors and Collaborators

    • M.D. Anderson Cancer Center
    • National Cancer Institute (NCI)
    • National Institutes of Health (NIH)

    Investigators

    • Principal Investigator: Carrie Daniel-MacDougall, PHD, M.D. Anderson Cancer Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    M.D. Anderson Cancer Center
    ClinicalTrials.gov Identifier:
    NCT00476632
    Other Study ID Numbers:
    • 2004-0112
    • P50CA100632
    • 5R01CA070917-08
    First Posted:
    May 22, 2007
    Last Update Posted:
    May 10, 2019
    Last Verified:
    May 1, 2019
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by M.D. Anderson Cancer Center
    Epidemiology
    Questionnaire
    Controls

    Study Results

    No Results Posted as of May 10, 2019