- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT04623736
Smartphone Application Smoking Cessation Study
Assessment of Smoking Cessation in a Publicly Available Cessation Smartphone Application
Descripción general del estudio
Descripción detallada
Cigarette smoking is the leading cause of preventable death in the U.S. and causes multiple cancers. Approximately 34 million U.S. adults currently smoke cigarettes, but over half of all smokers attempt to quit smoking each year. However, only about 6% quit successfully, in part, because many smokers make unassisted quit attempts, due to the lack of accessibility of cessation programs. Mobile health (mHealth) smoking cessation programs delivered through smartphone applications ('apps') can potentially reach a large number of smokers in the U.S., as 81% of U.S. adult smokers own a smartphone. The National Cancer Institute hosts Smokefree.gov, a suite of free, publicly available smoking cessation resources. In addition to web based and text-messaging resources, Smokefree.gov launched the quitSTART smartphone app in 2013, which is a publicly available smoking cessation app.
Participants in this study will be asked to complete a pre-cessation assessment, then download, install, and try to quit smoking using the smoking cessation smartphone application, quitSTART. Participants will be asked to use quitSTART for 4 weeks. Participants will also be asked to complete online surveys 2 and 4 weeks after the start of the study. To understand how people are using quitSTART, the investigators will collect quitSTART usage data from all participants (for example, how often someone opens quitSTART during the study period and what specific features someone uses).
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
Virginia
-
Charlottesville, Virginia, Estados Unidos, 22904
- University of Virginia
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Cigarette smoker
- Smoked at least 100 cigarettes
- Able to read and speak English
- Owns a smartphone
- 18 years of age or older
- USA resident
Exclusion Criteria:
- Not a cigarette smoker
- has not smoked at least 100 cigarettes
- Not able to read and speak English
- Does not own a smartphone
- Under 18 years of age
- Not a US resident
- Currently pregnant
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
---|---|
Experimental: quitSTART
|
All participants will have access to the Smokefree.gov
Initiative smoking cessation smartphone application, quitSTART.
This app is available, at no cost, to anyone who owns a smartphone and is interested in quitting smoking.
All smokers who download quitSTART are asked to provide basic information about themselves (e.g., age, sex, reason to quit smoking, triggers to smoke, when users typically smoke, how users plan to celebrate success, smoking frequency, age when started smoking regularly, ethnicity, race, cigarettes smoked per day), and set a quit date.
Information about cessation and challenges to help support quitting are available, as well as games and tracking features.
While using the app, users can proactively report cigarette cravings, if they slipped, if they are feeling "down" or feeling "great".
If a user reports a craving, they have the option to mark the timing or location of the craving and request a reminder to resist future cravings at the same time or location.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Self-reported 7-day smoking abstinence - 2 weeks
Periodo de tiempo: 2 weeks
|
"Have you smoked a cigarette (even a puff) in the past 7 days?"
self-reported by the participant
|
2 weeks
|
Self-reported 7-day smoking abstinence - 4 weeks
Periodo de tiempo: 4 weeks
|
"Have you smoked a cigarette (even a puff) in the past 7 days?"
self-reported by the participant
|
4 weeks
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Self-reported continuous smoking abstinence - 2 weeks
Periodo de tiempo: 2 weeks
|
"In the last two weeks, have you smoked at all?" self-reported by the participant
|
2 weeks
|
Self-reported continuous smoking abstinence - 4 weeks
Periodo de tiempo: 4 weeks
|
"In the last four weeks, have you smoked at all?" self-reported by the participant
|
4 weeks
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Kara P Wiseman, University of Virginia
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
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
Palabras clave
Otros números de identificación del estudio
- 3643
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
Marco de tiempo para compartir IPD
Tipo de información de apoyo para compartir IPD
- PROTOCOLO DE ESTUDIO
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.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .
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