- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00518388
Perceptions of Cervical Cancer Among Asian Americans
Perceptions of Cervical Cancer and Human Papillomavirus Among Asian Americans
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
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.
Undersøgelsestype
Tilmelding (Faktiske)
Kontakter og lokationer
Studiesteder
-
-
Texas
-
Houston, Texas, Forenede Stater, 77030
- University of Texas MD Anderson Cancer Center
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
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
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
---|---|
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.
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
---|---|
To learn about the beliefs, practices, and knowledge about cervical cancer among Asian American young adults
Tidsramme: 1 Year
|
1 Year
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
---|---|
To develop materials that will educate Asian Americans about cervical cancer and encourage them to get screened for this disease
Tidsramme: 1 Year
|
1 Year
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Richard A. Hajek, PHD, MS, BA, M.D. Anderson Cancer Center
Publikationer og nyttige links
Hjælpsomme links
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 2007-0101
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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-
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