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Cut Your Pressure Too: The Los Angeles Barbershop Blood Pressure Study

6 de julio de 2018 actualizado por: Ron Victor, Cedars-Sinai Medical Center

Barber-Pharmacist Coordination to Improve Blood Pressure Management in Black Men

African-American men suffer more than most other groups from hypertension (HTN) but often have less access and less contact with doctors. Previous work by the study's Principal Investigator in Dallas, Texas, and Altadena, California, showed that barbershops are an excellent place to identify black men with high blood pressure and to enlist the aid of their barbers as healthcare extenders.

The purpose of this study in Metro Los Angeles (LA) is to compare two types of barber-based patient-centered blood pressure programs to see which type is more effective in improving the customers' high blood pressure. One type emphasizes blood pressure medication and the other type emphasizes lifestyle modification for high blood pressure.

Descripción general del estudio

Descripción detallada

Uncontrolled hypertension (HTN) is one of the most important causes of premature disability and death among non-Hispanic black men. Indeed, black men have the highest HTN death rate of any U.S. race, ethnic, or gender group, contributing to a lower life expectancy. The age-adjusted HTN-related death rate is 3.3-times higher among black men than white men. To address this major health disparity, the investigators designed a novel community-partnered team approach to improve HTN management among black men and prevent needless strokes, heart attacks, kidney failure, and heart failure.

HTN requires physician (or middle-level provider) interaction to optimize blood pressure (BP) medication; black men have less interaction than black women; and thus far lower rates of HTN treatment (73% vs. 86%) and control (36% vs. 50%). Black-owned barbershops are a uniquely personal setting to discuss health with influential male peers. Barbershop health outreach is well-established, but untested as a vehicle for improving HTN control. Scientific evaluation is crucial to best allocate finite healthcare dollars and avoid promoting a "community health industry" that benefits only the promoters.

Under-treatment of HTN is common in primary care due to competing demands on physicians' time. The best way to improve HTN control is with team-based approaches enlisting pharmacists. They are more accessible than physicians, more knowledgeable about medication, and receive training on patient education. The investigators' new conceptual model links the barber-based intervention to team-based care delivery.

The purpose of this research study is to compare this new conceptual model to another barber-based patient-centered blood pressure program to see which is more effective in improving high blood pressure among Black patrons of African American owned barbershops in LA. Patrons randomized to Group 1 (the new conceptual model) will provide blood pressure readings for patrons aged 35 to 79 years of age and refer those with HTN to a Clinical Pharmacist to work with their doctors in optimizing blood pressure medication.

Patrons of Group 1 shops will also be exposed to role model posters are not intended as recruitment materials, but rather are educational tools that intend to highlight positive experiences of participation. The text of the role model stories will in no way provide statements of the effectiveness of the intervention being evaluated by the present research study. Rather, they are the main health messaging tools needed to promote completion of the program in order to achieve the experiences described. Essentially the document will be used as an intervention tool for peer-based health messaging - stories from real customers in the barbershop modeling target behaviors leading that promote continued participation in the protocol by peers with the hopes of achieving to the detection, treatment, and control of high blood pressure. Each role model story will encourage one of two desired health behaviors of potential subjects with elevated BP: 1) ask the barber to check patients' BP with each haircut, 2) schedule a follow-up visit with the study pharmacist to get patient's blood pressure under control. Large posters in the barbershop will show the model customer, his barber, and the study pharmacist who facilitated the desired behavior change. The model's (participants) own words will be used on the poster.

Group 2 barbershop patrons will be exposed to up-to-date information on high blood pressure and on lifestyle topics for blood pressure and heart health including weight management, healthy cooking, cholesterol lowering, and exercise.

A pre-specified cross-sectional sub study utilized the trial's initial screening population to test for an association between self-reported nocturia (>2 nightly/voids) and elevated daytime (in-barbershop) blood pressure.

Tipo de estudio

Intervencionista

Inscripción (Actual)

320

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

    • California
      • Los Angeles, California, Estados Unidos, 90048
        • Cedars-Sinai Medical Center

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

35 años a 79 años (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Masculino

Descripción

Inclusion Criteria:

  • 35 to 79 years of age
  • Non-Hispanic Black men
  • Long-term/frequent barbershop patronage (barbershop patrons having at least one haircut every 6 weeks in the same barbershop for the past 6 months).
  • Systolic BP >140 at 2 screenings on 2 separate days
  • Complete set of Baseline Data

Exclusion Criteria:

  • Women
  • Children
  • <35 years of age
  • Non-black
  • Hispanic ethnicity
  • New/infrequent patronage (<8 haircuts at same barbershop in last 12 months)
  • Systolic BP <140 at either screening
  • Currently receiving cancer chemotherapy
  • On Dialysis
  • Incomplete baseline data
  • Serious Plan to Move in the next 1.5 years
  • Plans to be out of the area for > 1 month in the next 1.5 years

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: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: BP measurement & pharmacy
BP measurements performed by barber, role model poster exposure in barbershop, and BP medication management visits with study pharmacist
Blood pressure monitoring by barber, blood pressure medication management by pharmacist, role model posters encouraging program participation
Otro: BP educational materials
Exposure to hypertension educational materials in barbershop
Exposure to hypertension educational materials

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Primary Blood Pressure Outcome - change in systolic blood pressure
Periodo de tiempo: 6 months
The pre-specified primary outcome was the change in systolic blood pressure from baseline to 6 months follow-up.
6 months

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Secondary Blood Pressure Outcome - change in diastolic blood pressure
Periodo de tiempo: 6 months
The change in diastolic blood pressure from baseline to 6 month follow-up
6 months
The percentage of participants achieving blood pressure goal
Periodo de tiempo: 6 months
The percentage of participants who achieved blood pressure goal after 6 months follow-up (140/90,135/85, 130/80)
6 months
The change in number/type of drug classes prescribed
Periodo de tiempo: 6 months
The change in number/class of prescription drugs prescribed from baseline to 6 month follow-up
6 months
Adverse Drug Reactions
Periodo de tiempo: 6 months
The number and type of adverse drug reactions reported from baseline to 6 month follow-up
6 months
Self-Rated Health
Periodo de tiempo: 6 months
The change in self-rated health score from baseline to 6 month follow-up
6 months
Self-Rated Patient Engagement
Periodo de tiempo: 6 months
The change in PACIC patient engagement score from baseline to 6 month follow-up
6 months

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Extension Study Primary Blood Pressure Outcome - change in systolic blood pressure
Periodo de tiempo: 12 months
The primary outcome of the extension study is the change in systolic blood pressure from baseline to 12 months follow-up.
12 months
Extension Study Secondary Blood Pressure Outcome - change in diastolic blood pressure
Periodo de tiempo: 12 months
The change in diastolic blood pressure from baseline to 12 month follow-up
12 months
Extension Study Secondary Outcome - the percentage of participants achieving blood pressure goal
Periodo de tiempo: 12 months
The percentage of participants who achieved blood pressure goal after 12 months follow-up (140/90,135/85, 130/80)
12 months
Extension Study Secondary Outcome - the change in number/type of drug classes prescribed
Periodo de tiempo: 12 months
The change in number/class of prescription drugs prescribed from baseline to 12 month follow-up
12 months
Extension Study Secondary Outcome - adverse drug reactions
Periodo de tiempo: 12 months
The number and type of adverse drug reactions reported from baseline to 12 month follow-up
12 months
Extension Study Secondary Outcome - self-rated health
Periodo de tiempo: 12 months
The change in self-rated health from baseline to 12 month follow-up
12 months
Extension Study Secondary Outcome - self-rated patient engagement
Periodo de tiempo: 12 months
The change in PACIC patient engagement score from baseline to 12 month follow-up
12 months

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

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)

17 de febrero de 2015

Finalización primaria (Actual)

30 de junio de 2017

Finalización del estudio (Actual)

9 de enero de 2018

Fechas de registro del estudio

Enviado por primera vez

17 de diciembre de 2014

Primero enviado que cumplió con los criterios de control de calidad

19 de diciembre de 2014

Publicado por primera vez (Estimar)

22 de diciembre de 2014

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

10 de julio de 2018

Última actualización enviada que cumplió con los criterios de control de calidad

6 de julio de 2018

Última verificación

1 de julio de 2018

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • Pro00035347
  • 5R01HL117983-02 (Subvención/contrato del NIH de EE. UU.)

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

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. .

Ensayos clínicos sobre BP measurement & pharmacy

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