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Incentives for Primary Care Use in a Safety Net Setting

11 de junio de 2018 actualizado por: Virginia Commonwealth University

Incentives for Primary Care Use: A Randomized Controlled Trial in a Safety Net Setting

A randomized controlled trial (RCT) of incentives for an initial primary care visit within 6 months of enrollment in a health care coverage program. Study subjects are drawn from a low-income adult population that gains coverage and access to community-based primary care services under a program administered by an academic safety-net hospital. The investigators will offer financial incentives to encourage an initial primary care visit within 6 months of enrollment and evaluate whether the primary care visit altered subsequent health seeking behavior and influenced patient satisfaction and other outcomes such as self-reported health status.

Descripción general del estudio

Descripción detallada

A randomized controlled trial (RCT) of incentives for an initial primary care visit within 6 months of enrollment in a health care coverage program. Study subjects are drawn from a low-income adult population that gains coverage and access to community-based primary care services under a program administered by an academic safety-net hospital. The investigators will offer financial incentives to encourage an initial primary care visit within 6 months of enrollment and evaluate whether the primary care visit altered subsequent health seeking behavior and influenced patient satisfaction and other outcomes such as self-reported health status.

Incentives should steer patients in their decision to seek primary care, reduce barriers to care, and ultimately improve patient health and reduce utilization and costs through their relationship with a PCP. This study is the first of its kind to incentivize low-income patients. This population has the greatest need for health care and exerts the greatest pressure on the United States' safety net system. Furthermore, the safety net population is the target of policies such as Medicaid eligibility expansions, yet urban safety net patients are largely understudied. These patients are rarely given the opportunity to participate in research, and when they are the subjects of measures to reduce health care utilization, they are the subject of policies using negative incentives such as those that introduce cost sharing for using ED services.1 Alternatively, safety net providers invest in case management systems to reduce utilization. The proposed study is a departure from prior measures to reduce utilization among low-income patients by focusing on patients and using positive incentives. The study borrows from the principles of behavioral economics to motivate patients towards primary care utilization. Once in the primary care system, The investigators will test whether primary care contact reduces more expensive forms (e.g., inpatient, ED) of health care.

The investigators will compare outcomes of patients assigned in the highest incentive group ($50) to patients assigned to the modest incentive group ($25) and to patients assigned to usual care (no incentive, but assignment to a PCP). The investigators will also compare incentive patients ($50, $25) to a contemporaneous group of patients that enroll in the safety net clinic at the same time.

Tipo de estudio

Intervencionista

Inscripción (Actual)

1228

Fase

  • No aplica

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

21 años a 64 años (Adulto)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Adults between ages 21-64 years
  • No prior enrollment in VCC for the past 12 months
  • English or Spanish speaking, and
  • Can be contacted by mail and telephone (preferably) or willing to be interviewed in person.

Exclusion Criteria:

  • Unable to be contacted by phone/mail
  • Cannot provide consent
  • No longer located in catchment area

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: Investigación de servicios de salud
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Sin intervención: Contemporaneous Control
This group is our 'usual care' control group. They were not contacted for an interview and were not offered an incentive to visit their primary care physician.
Comparador activo: $0 group
This group completed a baseline interview but was not offered any incentive if they visited their primary care physician.
Those assigned to the $0 group will not receive an incentive for visiting their PCP.
Experimental: $25 group
This group completed a baseline interview and was offered $25 they visited their primary care physician within 6 months.
Those assigned to the $25 group will receive $25 if they visit their PCP within 6 months of study enrollment.
Experimental: $50 group
This group completed a baseline interview and was offered $50 they visited their primary care physician within 6 months.
Those assigned to the $50 group will receive $50 if they visit their PCP within 6 months of study enrollment.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
The number of Primary Care Physician visits will be assessed using medical claims record data.
Periodo de tiempo: This will be assessed in the 6 months following study enrollment.
The number of primary care visits to a primary care physician will be collected from medical claims record data.
This will be assessed in the 6 months following study enrollment.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
The time to a Primary Care Physician will be assessed using medical claims record data.
Periodo de tiempo: This will be assessed in the 6 months following study enrollment.
The time to a primary care visits to a primary care physician will be collected from dates available in the medical claims record data.
This will be assessed in the 6 months following study enrollment.

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Cathy Bradley, Phd, PI

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

1 de enero de 2014

Finalización primaria (Actual)

8 de noviembre de 2016

Finalización del estudio (Actual)

8 de noviembre de 2016

Fechas de registro del estudio

Enviado por primera vez

28 de septiembre de 2016

Primero enviado que cumplió con los criterios de control de calidad

3 de octubre de 2016

Publicado por primera vez (Estimar)

4 de octubre de 2016

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

12 de junio de 2018

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

11 de junio de 2018

Última verificación

1 de junio de 2018

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • HM20000002
  • 1R01HS022534 (Subvención/Contrato de la AHRQ de EE. UU.)

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

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. .

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