- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07139132
- Juicio original
El estudio de Aha Oneida
Transformación de factores de riesgo en un alto riesgo de accidente cerebrovascular población nativa americana a través de un programa nutricional cultural
The purpose of this clinical trial is to learn whether a cultural nutritional program can change stroke risk factors, cognitive decline, and learn how school education programs about nutrition can improve health in the Oneida Nation.
Participants will undergo:
- A carotid ultrasound
- Cognitive testing
- Health assessment
- Blood work
- Health wellness coaching
Participants can expect to be in the study for 1 year.
Descripción general del estudio
Estado
Condiciones
Descripción detallada
The specific aims for this study are: 1) to determine if a cultural nutritional program across generations can change stroke risk factors in the Oneida Nation; 2) to determine if a cultural nutritional program across generations can change vascular cognitive decline in the Oneida Nation; and, 3) determine how structured culturally competent school education programs about nutrition influence knowledge of health. The intervention used is health wellness coaching. All individuals enrolled in this study will have opportunity to interact with an Oneida Nation employed Health wellness coach to find out about Oneida resources that they can use to modify their stroke risk factors.
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Stephanie Wilbrand, PhD
- Número de teléfono: 608-265-9248
- Correo electrónico: wilbrand@neurosurgery.wisc.edu
Ubicaciones de estudio
-
-
Wisconsin
-
Madison, Wisconsin, Estados Unidos, 53705
- Reclutamiento
- University of Wisconsin - Madison
-
Investigador principal:
- Robert Dempsey, MD
-
Contacto:
- Stephanie Wilbrand, PhD
- Número de teléfono: 608-265-9248
- Correo electrónico: wilbrand@neurosurgery.wisc.edu
-
Oneida, Wisconsin, Estados Unidos, 54155
- Reclutamiento
- Oneida Nation Reservation
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-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Age 7-85 years
- Receiving healthcare though the Oneida Comprehensive Health Division
Exclusion Criteria:
- Not Native American
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Prevención
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: School-age Native Americans
Participants who are age 7-17 and live with adult parent or guardian will answer a 10 question nutritional knowledge questionnaire. |
Health wellness coach will provide education and guidance about cultural nutrition Participants will undergo an ultrasound Educational program will teach students about healthy Native American food choices Participants will undergo a cognitive test. |
|
Experimental: Adult Native Americans
Adults age 18-85 |
Health wellness coach will provide education and guidance about cultural nutrition Participants will undergo an ultrasound Participants will undergo a cognitive test. Participants will undergo blood work. |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Cambio en el conocimiento de la salud a través de programas de educación escolar culturalmente competentes estructurados sobre nutrición
Periodo de tiempo: Línea de base a 1 año
|
Línea de base a 1 año
|
|
|
Change in incidence of stroke and transient ischemic attack (TIA)
Periodo de tiempo: Baseline to 1 year
|
Number of incidences of stroke or TIA during the study |
Baseline to 1 year
|
|
Change in number of participants that meet American Heart Association (AHA) Simple Rules for Diastolic Blood Pressure.
Periodo de tiempo: Baseline to 1 year
|
The AHA's simple rules for diastolic blood pressure: Normal = Less than 80 mm Hg; Elevated = Less than 80 mm Hg with a systolic reading of 120-129 mm Hg; Stage 1 Hypertension = 80-89 mm Hg; Stage 2 Hypertension = 90 mm Hg or higher; Hypertensive Crisis = Higher than 120 mm Hg (along with a systolic reading higher than 180 mm Hg). Researchers will be reporting the change in number of participants with diastolic blood pressure <90 mmHg. |
Baseline to 1 year
|
|
Change in number of participants that meet AHA's Simple Rules for Systolic Blood Pressure.
Periodo de tiempo: Baseline to 1 year
|
The AHA uses these simple rules for systolic blood pressure (the top number): Normal is less than 120, Elevated is 120-129, Stage 1 Hypertension is 130-139, and Stage 2 Hypertension is 140 or higher. A systolic reading of 180 or higher indicates a hypertensive emergency. Researchers will be reporting the change in number of participants with systolic blood pressure <140 mmHg. |
Baseline to 1 year
|
|
Change in number of participants that meet AHA Simple Rules for Body Mass Index (BMI)
Periodo de tiempo: Baseline to 1 year
|
The AHA uses the following guidelines for Body Mass Index (BMI) in adults: Underweight = Less than 18.5; Normal Weight = Between 18.5 and 24.9; Overweight = Between 25 and 29.9; and, Obesity = 30 or higher. Researchers will be reporting any improvement in BMI. |
Baseline to 1 year
|
|
Change in Montreal Cognitive Assessment (MoCA)
Periodo de tiempo: Baseline to 1 year
|
MoCA is scored out of a total of 30 points, with a score of 26 or above generally considered normal. The MoCA assesses various cognitive domains, including memory, visuospatial abilities, language, and executive functions. A lower score indicates potential cognitive impairment, with specific cutoffs for mild (19-23), moderate (10-18), and severe (0-9) impairment. |
Baseline to 1 year
|
|
Change in NIH Toolbox Score
Periodo de tiempo: Baseline to 1 year
|
NIH Toolbox Cognition Battery consists of tests of multiple constructs to asses for cognitive, sensory, motor and emotional function |
Baseline to 1 year
|
|
Change in Native American Acculturation Scale (NAAS)
Periodo de tiempo: Baseline to 1 year
|
NAAS is a 20-item questionnaire developed to assess the level of acculturation in Native Americans. It measures an individual's connection to both traditional Native American culture and mainstream American culture. Scores range from a low of 1, indicating low acculturation (or high Native American identity) to a high of 5, indicating high acculturation (or high mainstream American identity), with a score of 3 indicating "bicultural". The NAAS examines areas like identity, language, friendships, behaviors, attitudes, and generational/geographic background. |
Baseline to 1 year
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Change in nutrition knowledge
Periodo de tiempo: Baseline to 1 year
|
Change in knowledge will be assessed with pre-test, 1 year post-test of each participant to assess improvement in nutritional knowledge and understanding of healthy food options tied to Oneida culture. This will be assessed through a 10-question multiple choice survey about good versus bad nutrition choices. Participants will select their choices, low score indicates poor nutritional knowledge and high score indicating better understanding for healthy nutrition |
Baseline to 1 year
|
|
Change in plaque area
Periodo de tiempo: Baseline to 1 year
|
Measured via carotid ultrasound. |
Baseline to 1 year
|
|
Change in pulsatility index in carotid arteries
Periodo de tiempo: Baseline to 1 year
|
Measured via carotid ultrasound. This index is a unitless measurement calculated: peak systolic velocity - end diastolic velocity, divided by the mean velocity, higher values are thought to represent increased resistance to blood flow. |
Baseline to 1 year
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Robert Dempsey, MD, University of Wisconsin, Madison
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
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
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 2025-1171
- SMPH/NEURO SURG/NEURO SURG (Otro identificador: UW Madison)
- FA (Otro identificador: UW Madison)
- Protocol Version 10/23/26 (Otro identificador: UW Madison)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
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