- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT03196570
Increasing Physical Activity in Latino Men
Increasing Physical Activity in Latino Men Through Tailoring
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Physical Activity in Latino Men Through Tailoring is an individually randomized web and text message based pilot study, designed to increase physical activity amongst Latino men. The study is conducting formative research with a diverse population of Latino men to inform the adaptation of the Pasos Hacia La Salud web-based intervention, which was developed for Latina women, to an intervention focused on Latino men. Consideration will also be taken to ensure intervention material is culturally appropriate for Latino men of Caribbean, South and Central American origin. Half the study participants will be randomized into the intervention arm and half into the comparison group. Participants in the intervention arm will have access to a website where they can complete questionnaires, receive information, log their physical activity and set goals. Participants complete monthly questionnaires to establish their stage of change toward increasing their physical activity and receive information manuals based on their current stage of change. They will also have access to tip sheets via the study website and receive reoccurring text messages reminding them to log into the website. Participants in the comparison arm will have access to a similar website with information related to nutrition and overall wellness, not including physical activity.
The primary aims of this project are (1) to conduct formative research with a diverse population of RI Latino men to adapt the existing web-based interventions and add text message-based components to complement and enhance the intervention. The second primary aim is to determine the feasibility, acceptability, and preliminary efficacy of the intervention and the study recruitment, implementation and evaluation protocols with a diverse population of Latino men. An additional exploratory aim will be to examine potential moderators of treatment effects including demographics, acculturation, and environmental variables such as the neighborhood built, social and economic environments. The hypothesis is that participants randomized to the intervention condition will have greater increases in weekly minutes of physical activity after six months than those randomized to a wellness control condition. The results of this pilot study will inform a future randomized controlled trial with Latino men to increase PA.
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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-
Rhode Island
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Providence, Rhode Island, Estados Unidos, 02912
- Brown University
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Be sedentary ( participate in moderate intensity leisure time PA two days a week for less than 30 minutes a day, or less)
- Identify as a Latino male
- Speak Spanish
- Score of more than 16% on Spanish Shortened Test of Functional Health Literacy in Adults
- Own a cell phone with texting capabilities and have internet access
Exclusion Criteria:
- History of myocardial infarction or angina, insulin-dependent diabetes or hospitalization for diabetes in the past year, stroke, osteoarthritis, osteoporosis, orthopedic problems, or any medical condition that would make PA unsafe.
- Planning to move from the area in the next 6 months
- Hospitalization due to a psychiatric disorder in the past 3 years.
- BMI of 45 or higher and/or taking any medication that may impair PA tolerance or performance.
- If they or another family member is already enrolled in another PA or weight control study.
Plan de estudios
¿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: Intervention
After randomization into the intervention arm, participants will be instructed on how to use the Spanish language study website.
During the six month intervention, they will complete online questionnaires to determine their stage of change towards increasing physical activity.
A manual of information will be automatically generated based on their responses.
Participants can read this information online, along with tip sheets related to increasing physical activity.
On the website they can also set weekly goals and log their weekly PA.
It will also include short videos with demonstrations for PA they can do at home and around their neighborhood.
Information will also include community resources (community centers, public events, parks) where they can be physically active.
Participants will also receive prompts and encouragement via text-message to encourage them to log into the website and continue to track their progress.
|
After randomization into the intervention arm, participants will be instructed on how to use the Spanish language study website.
During the six month intervention, they will complete online questionnaires to determine their stage of change towards increasing physical activity.
A manual of information will be automatically generated based on their responses.
Participants can read this information online, along with tip sheets related to increasing physical activity.
On the website they can also set weekly goals and log their weekly PA.
It will also include short videos with demonstrations for PA they can do at home and around their neighborhood.
Information will also include community resources (community centers, public events, parks) where they can be physically active.
Participants will also receive prompts and encouragement via text-message to encourage them to log into the website and continue to track their progress.
|
|
Comparador activo: Contact Control
Participants in the control arm will attend the same baseline orientation sessions and measurements as the intervention arm.
After randomization into the control group, participants will complete an introductory in-person session to introduce them to a website, similar in design, with information on health topics other than physical activity, including diet and other factors associated with CVD risk.
It will include information from NHLBI heart health materials for Latinos.
Topics include healthy eating, increasing fruit and vegetable consumption, reducing fat and salt intake, learning about cholesterol, stress management.
Participants will log onto a separate website unique to the control group and complete monthly surveys on the wellness topics and their progress.
Participants will also receive prompts and encouragement text-messages to encourage them to log onto the website.
|
Participants in the control arm will attend the same baseline orientation sessions and measurements as the intervention arm.
After randomization into the control group, participants will complete an introductory in-person session to introduce them to a website, similar in design, with information on health topics other than physical activity, including diet and other factors associated with CVD risk.
It will include information from NHLBI heart health materials for Latinos.
Topics include healthy eating, increasing fruit and vegetable consumption, reducing fat and salt intake, learning about cholesterol, stress management.
Participants will log onto a separate website unique to the control group and complete monthly surveys on the wellness topics and their progress.
Participants will also receive prompts and encouragement text-messages to encourage them to log onto the website.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Change in Physical Activity from Baseline to 6 months
Periodo de tiempo: Baseline and 6 months
|
Minutes of Moderate and Vigorous Physical Activity
|
Baseline and 6 months
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Publicaciones y enlaces útiles
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
Otros números de identificación del estudio
- 1612001664
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.
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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