Path2Quit Tobacco Intervention For African Americans
27 de marzo de 2019 actualizado por: Case Comprehensive Cancer Center
Development and Pilot Evaluation of the Path2Quit Tobacco Intervention Targeting African Americans
The purpose of this research is to study a smoking cessation program for adult smokers in Northeast Ohio. The study will also look at how different people respond to the program.
The study includes completing surveys and receiving text messages to help participants become tobacco free.
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Descripción detallada
OBJECTIVES Specific Aim 1: Translate a culturally specific video-based tobacco use intervention into a scalable mobile health (mhealth) format.
Specific Aim 2: Conduct a pilot study of the video-text intervention.
Study Design:
2-arm semi-pragmatic randomized design among current tobacco users
Cuyahoga Metropolitan Housing Authority residents will be randomly assigned to receive (1) the newly translated Path2Quit or (2) SmokeFreeText (NCI's publicly available, standard text messaging program) combined with brief behavioral counseling session plus 2 weeks of nicotine replacement therapy (NRT). Primary outcomes will include intervention evaluations (content and format), acceptability, coping strategies, engagement, and NRT adherence. Secondary variables will include 24-hour quit attempts and biochemically verified tobacco use abstinence at the 1-month follow-up. Exploratory mediational analyses will examine the roles of urban hassles, acculturation, neighborhood environment, ethnic discrimination, and psychological distress in intervention effects.
Tipo de estudio
Intervencionista
Inscripción (Actual)
119
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
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Ohio
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Cleveland, Ohio, Estados Unidos, 44106
- Case Western Reserve University, Case Comprehensive Cancer Center
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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 y mayores (Adulto, Adulto Mayor)
Acepta Voluntarios Saludables
No
Géneros elegibles para el estudio
Todos
Descripción
Inclusion Criteria:
- Self-identify as African American
- Either smoke at least 1 cigarettes/day or have a carbon monoxide (CO) reading of at least 4 ppm
- Consistent with SmokefreeTXT, be willing to set a quit date within the next 14 days.
- Recruited from Cleveland metropolitan housing authority or who report low income based on federal guidelines
Exclusion Criteria:
- Does not meet all of the above inclusion criteria
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: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Path2Quit
Culturally specific text message intervention
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Path2Quit will deliver 20-60 second video clips by multimedia messaging service.
The message library will include 75-170 messages.
Written text messages will be limited to brief phrases to indicate the topic of the video.
Messages will be pushed to participants in the morning, in the afternoon, and 2 hours before the reported usual bedtime.
The cultural adaptations will be infused throughout the video segments.
Topics include deep structure: race and smoking in general, African American smoking statistics; norms for smoking; concerns about nicotine replacement/medication; family/collectivism; unique stressors; racism/discrimination, depression; co-morbid addiction; neighborhood/environmental influences; menthol cigarettes; race-specific weight issues and concerns; and working as a community against the tobacco industry.
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Comparador activo: SmokeFreeText
The National Cancer Institute's publicly available, standard text messaging program for tobacco cessation
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SmokefreeTXT is a 6-8 week fully automated text-based cessation intervention.
The program is free to U.S. subscribers who have a mobile phone, and is available on smokefree.gov
or by texting "QUIT" to short code 47848.
Participants are encouraged to set a quit date within the next 14 days, followed by count-down messages leading to the quit date.
Starting on the quit date, participants receive 6 weeks of intervention text messages, and assessment questions (mood, cravings, smoking status).
The message library contains 166 messages and 41 behavior change techniques,40 which are delivered at the greatest frequency during the first 2 weeks and taper over time.
When in need of assistance, participants can text one of 3 keywords (MOOD, CRAVE, or SLIP) to receive a relevant message from the system.
Participants can opt-out by texting STOP at any time.
With informed consent, we will be able to access the SmokefreeTXT data for these participants.
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Proportion of participants who abstain from smoking
Periodo de tiempo: At 1-month follow-up
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Abstinence will be coded as a binary variable.
Analysis will be conducted with an intent to treat approach
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At 1-month follow-up
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Number of missed nicotine replacement therapy doses
Periodo de tiempo: Up to 1-month follow-up
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Measure of NRT adherence.
Number of missed doses will be recorded for each participant
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Up to 1-month follow-up
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24-Hour quit attempts
Periodo de tiempo: At 1-month follow-up
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Number of times a participant quits smoking for at least 24 hours
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At 1-month follow-up
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Changes in carbon monoxide breath levels from baseline to followup
Periodo de tiempo: At 1-month follow-up
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Breath carbon monoxide tests will biochemically confirm self-reported cessation
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At 1-month follow-up
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Changes in Contemplation ladder score
Periodo de tiempo: From baseline to up to 1-month follow-up
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self-reported score 0-10 where a higher score indicates more readiness to quit
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From baseline to up to 1-month follow-up
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Average score of Intervention Evaluation (IRQ)
Periodo de tiempo: At 1-month follow-up
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The IRQ is a 22 item scale scored 0-7 (total score 0-154) where higher scores indicate more satisfaction
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At 1-month follow-up
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Average score of smoking urges
Periodo de tiempo: Up to 1-month follow-up
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This brief, 10 item scale is scores 1-7 (total score 10-70) with higher scores indicating greater agreement
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Up to 1-month follow-up
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Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Average scores of Urban hassles
Periodo de tiempo: Changes from baseline to 1 month follow-up
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This is a 63 item scale scored 0-5 (total score 0-315) where higher scores indicate more severe hassle
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Changes from baseline to 1 month follow-up
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Average Neighborhood Environment scale score
Periodo de tiempo: At Baseline
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The neighborhood environment scale is an 18 item True or False scale
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At Baseline
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Average General Ethnic Discrimination Scale Score
Periodo de tiempo: At baseline
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This is a measure of ethnic discrimination.
These 16 items are scored 1-6 (total score 16-96) with higher scores indicating greater levels of ethnic discrimination
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At baseline
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Average psychological distress score using the the perceived stress scale
Periodo de tiempo: At baseline
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A ten item scale with each item scored 0-4 (total score 0-40) where higher scores indicate more stress.
Positive items are scored in reverse.
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At baseline
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Average depression score using Center for Epidemiological Studies Depression (CES-D) Scale
Periodo de tiempo: At baseline
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A twenty item scale ranging from 0-60 with each item scored 0-3.
Higher scores indicate more depression
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At baseline
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Average Beliefs and Attitudes Survey Score
Periodo de tiempo: At baseline
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This is a 24 item scale (total range 24-168) with each item scored 1-7.
Higher scores indicate greater levels of agreement
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At baseline
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Average Ethnic Identity Score
Periodo de tiempo: At baseline
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This is based on the Multigroup Ethnic Identity Measure scale.
These five items are scored 1-4 for a total score of 5-20.
Higher scores indicate stronger ethnic identity
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At baseline
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Average Culturally Specific Interventions Expectancy Questionnaire
Periodo de tiempo: At baseline
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The Culturally Specific Interventions Expectancy Questionnaire is a 2 item scale with each item ranging 1-5 (total score 2-10) where higher scores indicate greater agreement.
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At baseline
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Investigadores
- Investigador principal: Monica Webb Hooper, PhD, Case Comprehensive Cancer Center
Publicaciones y enlaces útiles
La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.
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)
1 de abril de 2018
Finalización primaria (Actual)
20 de agosto de 2018
Finalización del estudio (Actual)
20 de agosto de 2018
Fechas de registro del estudio
Enviado por primera vez
30 de abril de 2018
Primero enviado que cumplió con los criterios de control de calidad
11 de mayo de 2018
Publicado por primera vez (Actual)
14 de mayo de 2018
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
28 de marzo de 2019
Última actualización enviada que cumplió con los criterios de control de calidad
27 de marzo de 2019
Última verificación
1 de marzo de 2019
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
- CASE1Y18
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
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