- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT04052386
Brief Alcohol Screening for Community College Students (BASICCS)
8 de agosto de 2019 actualizado por: Christine Lee, University of Washington
The present study focuses on examining the feasibility, acceptability, and preliminary effects of an adapted alcohol intervention for high-risk college students attending community colleges.
Investigators adapted BASICS (an efficacious in-person intervention developed for high-risk drinkers attending 4-year colleges and universities) to a web-conferencing format that allows the facilitator and participant to see and discuss live web-based personalized feedback.
SMS text messages with protective behavioral strategies were also provided.
The objective of the R34 was to establish feasibility and acceptability as well as to determine preliminary or likely effect sizes.
Descripción general del estudio
Descripción detallada
Young adulthood (ages 18-29) is associated with increased risk for alcohol-related negative consequences; however, little is known about effective interventions for young adults attending community colleges (CCs).
Thus, it is critical to develop an intervention that meets the various needs and demanding lifestyles of CC students.
The investigators proposed to develop a user-friendly and convenient intervention that addresses relevant social norms, the impact of high-risk alcohol use on health and well-being in relevant life domains beyond student life and academic achievement, and provides ongoing exposure to behavior change strategies.
To address the notable differences between CC students and traditional 4-year students, the investigators adapted BASICS to a web-conferencing format that allows the facilitator and participant to see and discuss live web-based personalized feedback (FB).
This intervention for CC students, BASICCS, will focus on relevant normative feedback and alcohol's impact on multiple roles and personal goals of the CC student.
Providing tips and protective behavioral strategies (PBS) after BASICS interventions via handouts or mailed postcards is standard practice and with preliminary evidence supporting the use of mobile phone text messaging (TM) or short message service (SMS) to reduce heavy-episodic drinking; thus, in this study SMS text messages were used to deliver ongoing protective behavioral strategies (PBS) the month after participating in the BASICCS session.
The objective of this research was to establish feasibility and acceptability as well as to determine preliminary or likely effect sizes.
CC student drinkers were recruited to participate and if eligible, they were randomized to one of two conditions (BASICCS or assessment-only control) and completed 1- and 3-month follow-ups.
Tipo de estudio
Intervencionista
Inscripción (Actual)
142
Fase
- No aplica
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Ubicaciones de estudio
-
-
Washington
-
Seattle, Washington, Estados Unidos, 98105
- University of Washington
-
-
Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
18 años a 29 años (Adulto)
Acepta Voluntarios Saludables
Sí
Géneros elegibles para el estudio
Todos
Descripción
Inclusion Criteria:
- being 18-29 years old; enrolled full- or part-time at one of the three community colleges where data collection took place; consuming 4+/5+ drinks for women/men on one occasion in the past month or exceeding weekly NIAAA drinking recommendations (8+/15+ for women/men); and possessing a cell phone with text-messaging capability
Exclusion Criteria:
- not meeting inclusion criteria, not consenting to participate
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Prevención
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: BASICCS
Participants randomized to the BASICCS condition received a personalized feedback intervention conducted through a web-conferencing platform.
They also received up to 24 text messages with protective behavioral strategies for drinking during the following month.
|
Participants randomized to the BASICCS condition received a personalized feedback intervention conducted through a web-conferencing platform.
The personalized feedback intervention included tailored feedback on drinking quantity and frequency of alcohol, BAC, alcohol-related consequences, normative perceptions of peer drinking, alcohol outcome expectancies, family history of risk, and financial costs of alcohol.
They also received up to 24 text messages with protective behavioral strategies for drinking during the following month.
|
|
Sin intervención: Control
Participants randomized to the control group did not receive any intervention.
They were an assessment-only control group.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Daily Drinking Questionnaire
Periodo de tiempo: 1-month
|
Number of standard drinks consumed each day of typical week past month
|
1-month
|
|
Daily Drinking Questionnaire
Periodo de tiempo: 3-month
|
Number of standard drinks consumed each day of typical week past month
|
3-month
|
|
Frequency of Binge Drinking
Periodo de tiempo: 1-month
|
Number of times in past month engaged in heavy episodic drinking (4+ drinks for women, 5+ drinks for men)
|
1-month
|
|
Frequency of Binge Drinking
Periodo de tiempo: 3-month
|
Number of times in past month engaged in heavy episodic drinking (4+ drinks for women, 5+ drinks for men)
|
3-month
|
|
Estimated Blood Alcohol Concentration (eBAC)
Periodo de tiempo: 1-month
|
estimated peak blood alcohol concentration
|
1-month
|
|
Estimated Blood Alcohol Concentration (eBAC)
Periodo de tiempo: 3-month
|
estimated peak blood alcohol concentration
|
3-month
|
|
Brief Young Adult Alcohol Consequences Questionnaire
Periodo de tiempo: 1-month
|
Number of alcohol-related consequences endorsed
|
1-month
|
|
Brief Young Adult Alcohol Consequences Questionnaire
Periodo de tiempo: 3-month
|
Number of alcohol-related consequences endorsed
|
3-month
|
Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Investigadores
- Investigador principal: Christine M Lee, PhD, University of Washington
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Actual)
20 de enero de 2017
Finalización primaria (Actual)
26 de junio de 2017
Finalización del estudio (Actual)
26 de junio de 2017
Fechas de registro del estudio
Enviado por primera vez
7 de agosto de 2019
Primero enviado que cumplió con los criterios de control de calidad
8 de agosto de 2019
Publicado por primera vez (Actual)
9 de agosto de 2019
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
9 de agosto de 2019
Última actualización enviada que cumplió con los criterios de control de calidad
8 de agosto de 2019
Última verificación
1 de agosto de 2019
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 50262
- R34AA023047 (Subvención/contrato del NIH de EE. UU.)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
SÍ
Descripción del plan IPD
We plan to share limited datasets for the purposes of data analysis and dissemination.
Marco de tiempo para compartir IPD
Data dictionaries and limited datasets can be made available starting in September 2020.
Criterios de acceso compartido de IPD
Individual requests to access data with intended purpose should be made to Dr. Lee and will be reviewed by the investigative team.
Tipo de información de apoyo para compartir IPD
- PROTOCOLO DE ESTUDIO
- SAVIA
- CIF
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
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. .