African American Cancer Prevention Project: Establishing a Cohort to Investigate Health Disparities

Cancer Clinical Trial

Official title:

African American Cancer Prevention Project: Establishing a Cohort to Investigate Health Disparities

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT00823394
• Other study ID #: 2007-0970
• Status: Active, not recruiting
• Start date: December 5, 2008
• Est. completion date: December 31, 2020

Study information

• Verified date: January 2020
• Source: M.D. Anderson Cancer Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The goal of this research study is to learn if certain factors may affect cancer rates among African Americans. These factors include behavioral, social, and environmental factors including diet and physical activity, cigarette smoking, cancer screening, health care, neighborhood environment, and mental health.

Description:

Study Procedures:

If you decide to take part in this study, you will complete study procedures at month 36 (the day you sign this consent form) and again every year for the next 2 years. These procedures include completing a questionnaire, having your body measurements taken, and receiving self-help materials.

At month 36, you will complete the questionnaire on a computer that is set up at the church in a private room. The questions will be about nutrition, exercise, tobacco and alcohol use, your neighborhood, age, education, social status, health status, stress, and racism. It should take about 75 minutes to complete. Your waist, hip, height, and weight will also be measured while you are in the private room.

Every year after that for the next 2 years, you will go back to the church to complete a new questionnaire each time. The questionnaires should take about 75 minutes to complete each time.

If you cannot get back to the church, you may complete the questionnaire over the phone. The study staff will provide you with the phone number and directions on how to complete the survey over the phone. Your measurements will be taken at the church, or at the Behavioral Research and Treatment Center (BRTC) at MD Anderson, whichever is more convenient for you.

At each study visit, you will also receive self-help materials on how to lower your risk for developing cancer.

Questionnaire Data:

Your questionnaire data will be used for research purposes only. Your responses will not be shared with your personal doctor. If you feel you need a doctor's opinion about anything that is asked about in the questionnaire (such as mental or emotional difficulties or symptoms), please contact your personal physician.

About 1 month after each you complete the questionnaire each time, the research staff will review and score your responses. If your scores suggest signs of depression, you will be given a list of resources for mental health screening.

Length of Study:

After 5 years, your active participation in this study will be over. You may be contacted in the future to see if you would agree to take part in other research studies.

This is an investigational study.

Up to 1,501 people will take part in this study. All will be enrolled at MD Anderson.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 1500
• Est. completion date: December 31, 2020
• Est. primary completion date: December 31, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. be age 18 years old and above

2. read and write English

3. live in the Houston metro area

4. have a viable (working) telephone number and home address

Exclusion Criteria:

1) None.

Related Conditions & MeSH terms

• Cancer

Intervention

Behavioral:
• Questionnaire
Completed privately via computer at Windsor Village Church, approximately 75 minutes. Repeated at Months 12 and 24.

Other:
• Body Measurements
Waist, hip, height, and weight measured privately. Repeated at Months 12 and 24.

Behavioral:
• Self-help Materials
Information on how to lower risk for developing cancer.

Locations

Country	Name	City	State
United States	University of Texas MD Anderson Cancer Center	Houston	Texas

Sponsors (1)

Lead Sponsor	Collaborator
M.D. Anderson Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Feasibility Study Establishing African American Cancer Prevention Project (AACP)	A longitudinal study to learn if and how certain behavioral, social, and environmental factors may affect cancer rates among African Americans as compared to other racial and ethnic groups.	2 Years

External Links

•   University of Texas MD Anderson Cancer Center Website