- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00518388
Perceptions of Cervical Cancer Among Asian Americans
Perceptions of Cervical Cancer and Human Papillomavirus Among Asian Americans
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Survey:
If you agree to take part in this study, you will complete a survey about your health practices and knowledge about cervical cancer and HPV. You will also be asked to provide some personal history on yourself such as your age, gender, birthplace, ethnicity, relationship status and educational level. Female participants will be asked to indicate if they have received an HPV test (also called a "Pap" test) within the last 3 years. The survey will take about 5-10 minutes to complete and will be filled out on the same day as the focus group.
Focus Group:
You will also take part in a discussion group called a "focus group." A trained focus group leader will guide you and 8-10 others through a series of questions. He/she will lead a discussion to hear comments, opinions, and observations on a brochure and poster about cervical cancer and HPV. Groups will be made up of participants of the same gender (that is, all male or all female) and ethnic group (Filipino, Korean, or Vietnamese). Each discussion group will last about 2 hours and may be audiotaped so that the discussion may be transcribed and analyzed. You will only be called by your first name and you are not required to use your real name during the focus group discussion. You will not be identified by the audiotape recordings.
Length of Study:
When the focus group discussion is over, you will be off-study.
This is an investigational study. Up to 60 participants will be enrolled on this study. All will be enrolled at M. D. Anderson.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Texas
-
Houston, Texas, United States, 77030
- University of Texas MD Anderson Cancer Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Self identified as Korean, Filipino, or Vietnamese
- Individuals 18-29 years of age
- Have a high school education or less (but not less than 4th grade)
- Able to read and speak English and one of these languages: Korean, Vietnamese, or Tagalog
- Lower socioeconomic status, defined as: for a household of 1, not more than $18,620 annual income, for a household of 2, not more than $24,980, for a household of 3, not more than $31,340, for a household of 4, not more than $37,700, for a household of 5, not more than $44,060, for a household of 6,not more than $50,420, for a household of 7, not more than $56,780 NOTE: The CDC has granted some flexibility with these income guidelines
- Not currently pregnant
Exclusion Criteria:
1) Household income greater than 200% of the federal poverty level
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Focus Group + Questionnaire
Participants that are self identified as Korean, Filipino, or Vietnamese.
|
Focus groups each lasting about 2 hours.
Questionnaire relating to your health practices and knowledge about cervical cancer and HPV.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
To learn about the beliefs, practices, and knowledge about cervical cancer among Asian American young adults
Time Frame: 1 Year
|
1 Year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
To develop materials that will educate Asian Americans about cervical cancer and encourage them to get screened for this disease
Time Frame: 1 Year
|
1 Year
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Richard A. Hajek, PHD, MS, BA, M.D. Anderson Cancer Center
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2007-0101
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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