Completado

Improving Survey Procedures for Young Men Who Have Sex With Men in Web-based HIV Prevention: Retention Study

0 criterios cumplidosConsulta de un vistazo cómo tu perfil cumple con cada criterio de elegibilidad.
Qué se está evaluando

Monetary Incentive

+ Altruistic Incentive

+ Dashboard Incentive

Conductual
Quiénes están siendo reclutados

De 18 a 34 años
+7 Criterios de eligibilidad
Ver todos los criterios de elegibilidad
Cómo está diseñado el estudio

Intervencional
Inicio del estudio: abril de 2015
Ver detalles del protocolo

Resumen

Patrocinador PrincipalEmory University
Última actualización: 27 de enero de 2026
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Fecha de inicio: 1 de abril de 2015

Fecha en la que se inscribió al primer participante.

Men who have sex with men (MSM) are the risk population most heavily impacted by HIV in the United States by any measure; in 2009, at least 61% of new HIV infections were estimated to have occurred in MSM. MSM are experiencing an increase in HIV transmission that has been occurring since at least 1990, and accelerated in multiple North American and European countries from 2000-2005. The expansion of the HIV epidemic has been proposed to be attributable, in part, to the extent to which the internet has facilitated sexual connectivity among MSM. Researchers have attempted to reach MSM for HIV prevention research and intervention on the internet. In the past 10 years, there has been a proliferation of internet surveys and HIV research studies among men who have sex with men that utilize the internet for data collection and, in some cases, the delivery of HIV prevention content. The development of internet-based interventions has been recently identified as especially promising because of its potential for scalability. However, there are also important limitations to internet-based data collections and prevention studies. The most important of these relate to representativeness and opportunities to introduce bias to data collections and differences in access to and use of internet among different subgroups of MSM. Equally important, although less discussed, are the unique ethical and human research protections challenges posed by online sexual health prevention studies. The investigators will conduct an experiment to improve knowledge of how to conduct internet-based HIV prevention research with MSM in ways that decrease biases in data collections. The design will consist of a randomized controlled trials of MSM recruited online. A total of 1000 MSM will be enrolled to determine how to best improve retention in online surveys.

Título OficialImproving Survey Procedures for Young Men Who Have Sex With Men in Web-based HIV Prevention: Retention Study
NCT02424643
Patrocinador PrincipalEmory University
Última actualización: 27 de enero de 2026
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Protocolo

Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.
Detalles del Diseño

Se reclutarán 1131 pacientes

Número total de participantes que el ensayo clínico espera reclutar.



Elegibilidad

Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.
Criterios

Hombre

Sexo biológico de los participantes elegibles para inscribirse.

De 18 a 34 años

Rango de edades de los participantes que pueden unirse al estudio.

Voluntarios sanos permitidos

Indica si personas sanas, sin la condición que se estudia, pueden participar.

Criterios

3 criterios de inclusión requeridos para participar
male

aged 18 to 34 years

have had sex with another man in the past 12 months

4 criterios de exclusión impiden participar
female or transgender

younger than 18 years of age

older than 34 years of age

have not had sex with another man in the past 12 months.

Plan de Estudio

Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.
Grupos de Tratamiento
Objetivos del Estudio

3 grupos de intervención están designados en este estudio

0% de probabilidad de ser asignado al grupo placebo

Grupos de Tratamiento

Grupo I

Experimental
Participants in this arm will receive a $20 Amazon.com incentive for participating in the online survey.

Grupo II

Experimental
Participants in this arm will receive altruistic messages throughout the length of the survey in hopes of improving survey completion.

Grupo III

Experimental
Participants in this arm will receive a dashboard at the end of the survey that will compare their data entered into the survey to other participants who have taken the survey. A preview of this dashboard will be shown at the beginning of the survey as a teaser in the hopes to improve survey completion.

Objetivos del Estudio

Objetivos Primarios

Centros del Estudio

Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.

Este estudio tiene una ubicación

Suspendido

Rollins School of Public Health, Emory University

Atlanta, United StatesAbrir Rollins School of Public Health, Emory University en Google Maps
Completado1 Centros de Estudio