African American Cancer Prevention Project: Establishing a Cohort to Investigate Health Disparities
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00823394|
Recruitment Status : Active, not recruiting
First Posted : January 15, 2009
Last Update Posted : January 27, 2020
|Condition or disease||Intervention/treatment|
|Cancer||Behavioral: Questionnaire Other: Body Measurements Behavioral: Self-help Materials|
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.
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.
|Study Type :||Observational|
|Actual Enrollment :||1500 participants|
|Official Title:||African American Cancer Prevention Project: Establishing a Cohort to Investigate Health Disparities|
|Actual Study Start Date :||December 5, 2008|
|Estimated Primary Completion Date :||December 31, 2020|
|Estimated Study Completion Date :||December 31, 2020|
Windsor Village United Methodist Church
Questionnaire + Body Measurements + Self-help Materials
Completed privately via computer at Windsor Village Church, approximately 75 minutes. Repeated at Months 12 and 24.
Other Name: Survey
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.
- Feasibility Study Establishing African American Cancer Prevention Project (AACP) [ Time Frame: 2 Years ]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.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00823394
|United States, Texas|
|University of Texas MD Anderson Cancer Center|
|Houston, Texas, United States, 77030|
|Principal Investigator:||Lorna H. McNeill, MPH, PhD||M.D. Anderson Cancer Center|