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Epidemiology Controls Using Healthy Participants

Conditions
Healthy
Interventions
Behavioral: Questionnaire
Registration Number
NCT00476632
Lead Sponsor
M.D. Anderson Cancer Center
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.

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.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
1500
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
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Exclusion Criteria
  1. Individuals with prior cancer
  2. Individuals under the age of 18
Read More

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
ControlQuestionnairePerson with no history of cancer.
Primary Outcome Measures
NameTimeMethod
To identify biologic and lifestyle factors that may increase a person's risk of developing certain types of cancer.6 Years
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Texas MD Anderson Cancer Center

🇺🇸

Houston, Texas, United States

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