- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07856563
Vaccine Knowledge, Attitudes and Practices Among Men Who Have Sex With Men: a Global Cross-sectional Study (VAC-M)
This study aims to investigate vaccine-related knowledge, attitude, vaccine confidence and vaccine hesitancy among MSM across multiple countries and regions.
Descripción general del estudio
Tipo de estudio
Inscripción (Estimado)
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Huachun Zou
- Número de teléfono: +86-21-54237707
- Correo electrónico: zouhuachun@fudan.edu.cn
Copia de seguridad de contactos de estudio
- Nombre: Feiyang Yin
- Número de teléfono: +86 18008631217
- Correo electrónico: fyyin25@m.fudan.edu.cn
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Método de muestreo
Población de estudio
Self-identify as MSM, with eligibility in certain participating countries and regions potentially extended to transgender women and non-binary individuals who have sexual relations with men, using the same questionnaire.
Descripción
Inclusion Criteria:
-
Participants will be eligible for the study if they meet all of the following conditions:
- Have resided in a participating country or region for at least six months.
- Are aged 18 years or older.
- Self-identify as MSM, with eligibility in certain participating countries and regions potentially extended to transgender women and non-binary individuals who have sexual relations with men, using the same questionnaire.
Exclusion Criteria:
-
Participants will be excluded if they meet any of the following conditions:
- Are aged under 18 years.
- Decline to participate in the study or fail to complete the informed consent process.
- Have not resided, or do not currently reside, in a participating country or region.
- Submit duplicate responses from the same IP address or device.
- Fail data quality checks, including automated or fraudulent submissions and failure to pass human verification procedures.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Modelos observacionales: CASE_ONLY
- Perspectivas temporales: CROSS_SECTIONAL
Cohortes e Intervenciones
Grupo / Cohorte |
Intervención / Tratamiento |
|---|---|
|
Hombres que tienen sexo con hombres
|
No interventions because it is a observational cross-sectional study |
|
transgender women and non-binary individuals
transgender women and non-binary individuals who have sexual relations with men |
No interventions because it is a observational cross-sectional study |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Vaccine uptake
Periodo de tiempo: Baseline, at enrollment in this cross-sectional study
|
Percentage(%) of participants who have received at least one dose of HPV vaccine, assessed by self-reported vaccination history |
Baseline, at enrollment in this cross-sectional study
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Vaccine knowledge
Periodo de tiempo: Baseline, at enrollment in this cross-sectional study
|
Vaccine knowledge will be measured based on participants' scores on the vaccine knowledge items included in the study questionnaire, which will assess general vaccine knowledge and HPV vaccine-specific knowledge. Responses to individual items will be scored according to the predefined scoring criteria and summed to generate domain-specific knowledge scores. Higher scores indicate greater knowledge in the corresponding domain. |
Baseline, at enrollment in this cross-sectional study
|
|
Vaccine attitude
Periodo de tiempo: Baseline, at enrollment in this cross-sectional study
|
Vaccine attitudes will be measured based on participants' scores on the Vaccination Attitudes Examination Scale included in the study questionnaire, which assesses four dimensions of vaccination attitudes: mistrust of vaccine benefits, worries about unforeseen future effects, concerns about commercial profiteering, and preference for natural immunity. Responses to individual items will be scored according to the predefined scoring criteria and combined to generate an overall vaccine attitude score. Higher scores indicate more negative attitudes toward vaccination. |
Baseline, at enrollment in this cross-sectional study
|
|
Vaccine confidence
Periodo de tiempo: Baseline, at enrollment in this cross-sectional study
|
Vaccine confidence will be measured based on participants' scores on the Vaccine Confidence Index included in the study questionnaire, which assesses perceptions of vaccine importance, safety, effectiveness, and compatibility with religious beliefs. Responses to individual items will be scored according to the predefined scoring criteria and combined to generate an overall vaccine confidence score. Higher scores indicate greater confidence in vaccines. |
Baseline, at enrollment in this cross-sectional study
|
|
Vaccine hesitancy
Periodo de tiempo: Baseline, at enrollment in this cross-sectional study
|
Vaccine hesitancy will be measured based on participants' scores on the Vaccine Hesitancy Scale included in the study questionnaire. The scale assesses participants' perceptions of vaccine importance and effectiveness, trust in vaccine information and recommendations, perceived benefits of vaccination, and concerns about vaccine risks and adverse effects. Responses to individual items will be scored according to the predefined scoring criteria and summed to generate a total vaccine hesitancy score. Higher total scores indicate greater vaccine hesitancy. |
Baseline, at enrollment in this cross-sectional study
|
Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Otros números de identificación del estudio
- H2026163
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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