- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT00518388
Perceptions of Cervical Cancer Among Asian Americans
Perceptions of Cervical Cancer and Human Papillomavirus Among Asian Americans
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
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.
Type d'étude
Inscription (Réel)
Contacts et emplacements
Lieux d'étude
-
-
Texas
-
Houston, Texas, États-Unis, 77030
- University of Texas MD Anderson Cancer Center
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
La 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
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
Intervention / Traitement |
|---|---|
|
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.
Autres noms:
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
To learn about the beliefs, practices, and knowledge about cervical cancer among Asian American young adults
Délai: 1 Year
|
1 Year
|
Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
|
To develop materials that will educate Asian Americans about cervical cancer and encourage them to get screened for this disease
Délai: 1 Year
|
1 Year
|
Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Les enquêteurs
- Chercheur principal: Richard A. Hajek, PHD, MS, BA, M.D. Anderson Cancer Center
Publications et liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 2007-0101
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .