African American Church-based Cohort

This study is currently recruiting participants.
Verified April 2013 by M.D. Anderson Cancer Center
Sponsor:
Information provided by (Responsible Party):
M.D. Anderson Cancer Center
ClinicalTrials.gov Identifier:
NCT00823394
First received: January 14, 2009
Last updated: April 18, 2013
Last verified: April 2013

January 14, 2009
April 18, 2013
December 2008
December 2014   (final data collection date for primary outcome measure)
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. [ Time Frame: 2 Years ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00823394 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
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African American Church-based Cohort
African American Cancer Prevention Project: Establishing a Cohort to Investigate Health Disparities

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.

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.

Observational
Observational Model: Case Control
Time Perspective: Prospective
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Probability Sample

Adult attendees of Windsor Village United Methodist Church living in Houston.

Cancer
  • Behavioral: Questionnaire
    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.
Windsor Village United Methodist Church
Questionnaire + Body Measurements + Self-help Materials
Interventions:
  • Behavioral: Questionnaire
  • Other: Body Measurements
  • Behavioral: Self-help Materials
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
1501
Not Provided
December 2014   (final data collection date for primary outcome measure)

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.

Both
18 Years and older
Yes
Contact: Crystal Roberson, MPH 713-794-1074
United States
 
NCT00823394
2007-0970
No
M.D. Anderson Cancer Center
M.D. Anderson Cancer Center
Not Provided
Principal Investigator: Lorna H. McNeill, MPH, PhD UT MD Anderson Cancer Center
M.D. Anderson Cancer Center
April 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP