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Diabetes Prevention Program for the Treatment of Nonalcoholic Fatty Liver Disease

28 de julio de 2021 actualizado por: Amreen Dinani, Icahn School of Medicine at Mount Sinai

Pilot Study: Diabetes Prevention Program for the Treatment of Nonalcoholic Fatty Liver Disease

Nonalcoholic fatty liver disease (NAFLD) is a rapidly growing epidemic worldwide and is an increasingly important etiology of chronic liver disease and hepatocellular carcinoma. NAFLD affects approximately 90 million people in the United States (US) amounting to an annual cost of $100 billion yearly. It is projected to become the leading cause of liver transplantation in the US by 2030 and is associated with significant morbidity and mortality. NAFLD is a spectrum of liver diseases, ranging from simple steatosis (nonalcoholic fatty liver, NAFL) to hepatic steatosis associated with inflammation (nonalcoholic steatohepatitis, NASH), which can be associated with liver scarring (hepatic fibrosis) and cirrhosis. There are limited therapeutic options that have been shown to effectively reduce or reverse the progression of disease.

Lifestyle modification is the backbone of therapy, but difficult to achieve. A modest amount of weight loss of approximately 3% can reduce liver steatosis and a 10% weight loss can reduce the NASH and improve liver fibrosis. The American Association of the Study of Liver Diseases (AASLD) guidelines state that "a combination of a hypocaloric diet (daily reduction by 500-1000 kcal) and moderate intensity exercise is the best likelihood of sustaining weight loss over time." There are several barriers to adopting a healthy lifestyle involving both patient and physician limitations. The aim of this study is to engage patients in a lifestyle intervention program that has already been shown to be successful in achieving weight loss goals and adopting healthier lifestyle patterns.

The CDC Diabetes Prevention Program, (DPP) was a large (n=3,234) multicenter study aimed to evaluate the effect of lifestyle intervention or treatment with metformin on the incidence of type 2 diabetes (T2DM). Lifestyle intervention reduced the incidence of T2DM by 58% (95% CI, 48-66%) and metformin reduced the incidence by 31% (95% CI, 17-43%) as compared to placebo. To prevent one case of diabetes over three years, 6.9 persons would have to participate in the lifestyle-intervention program, and 13.9 would have to receive metformin. The CDC DPP program has been adapted and tested in the multiple different community and state-wide programs including the YMCA, WorkWellNYC and NYS DPP. In these real-world models, the life style intervention program has been delivered in a group-based format by DPP lifestyle coaches. These programs have been successful like that of the randomized trial and improvements were sustainable at 6 and 12 month follow up after completion of the program. The program is now available and reimbursable through Medicare (Medicare Diabetes Prevention Program).

In this pilot study, the researchers will enroll 20 patients with NAFLD in an adapted DPP program and follow study participants for 1 year. The rationale for the proposed research is to apply the DPP to NAFLD because of the close relationship with Diabetes and determine the real-world outcome of the DPP program on weight loss in patients with NAFLD. If the researchers illustrate that weight loss can be achieved and is sustainable in patients with NAFLD enrolled in lifestyle intervention programs, the researchers can develop innovative approaches to deliver such a program nationwide in a cost-effective and sustainable manner.

Descripción general del estudio

Estado

Terminado

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Actual)

20

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

    • New York
      • New York, New York, Estados Unidos, 10003
        • Mount Sinai Union Square

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:

  • diagnosis of NAFLD, defined by the presence of hepatic steatosis with vibration controlled transient elastography (VCTE) controlled attenuation parameter (CAP) measurement over 240dB/m, or liver biopsy showing macrovesicular steatosis in ≥ 5% of hepatocytes.
  • patients were 18 years and older,
  • fluent in English (the program could only be conducted in English by the DPP-certified coach),
  • able to meet program scheduling requirements, and able to participate in physical activity.

Exclusion Criteria:

  • additional causes of liver disease such as viral hepatitis, biliary obstruction, hepatocellular carcinoma, Wilson's disease, Budd Chiari Syndrome, autoimmune hepatitis, alcoholic liver disease or alcohol use (>20g/day women, >30g/day men),
  • aspartate aminotransferase (AST) or alanine aminotransferase (ALT) values >300 U/L,
  • using steatogenic medications (amiodarone, methotrexate, tamoxifen, and corticosteroids),
  • pregnant,
  • a history of liver transplantation.

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: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Treatment Arm
Patients enrolled in 1 year program
The Diabetes Prevention Program is a 1 year validated program to prevent the development of type 2 diabetes. Participants with NAFLD will engage will work with a CDC certified DPP certified lifestyle coach and other participants in a group setting during the study focusing on lifestyle changes to achieve weight loss and improvement in NAFLD.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Number of participants in the program at the end of the study
Periodo de tiempo: 12 months
Retention defined as number of patients in the program at the end of the study
12 months

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in Weight
Periodo de tiempo: baseline and 12 months
Change in Weight at 12 months as compared to baseline
baseline and 12 months
Hepatic steatosis via Fibroscan
Periodo de tiempo: Baseline
Changes in hepatic steatosis measured with fibroscan using the controlled attenuated parameter.
Baseline
Hepatic steatosis via Fibroscan
Periodo de tiempo: 6 months
Changes in hepatic steatosis measured with fibroscan using the controlled attenuated parameter .
6 months
Hepatic steatosis via Fibroscan
Periodo de tiempo: 12 months
Changes in hepatic steatosis measured with fibroscan using the controlled attenuated parameter.
12 months
Glycosylated A1C
Periodo de tiempo: Baseline
Glycosylated A1C in assessing metabolic comorbidity
Baseline
Glycosylated A1C
Periodo de tiempo: 6 months
Glycosylated A1C in assessing metabolic comorbidity
6 months
Glycosylated A1C
Periodo de tiempo: 12 months
Glycosylated A1C in assessing metabolic comorbidity
12 months
Lipid levels
Periodo de tiempo: Baseline
Lipid levels in assessing metabolic comorbidity
Baseline
Lipid levels
Periodo de tiempo: 6 months
Lipid levels in assessing metabolic comorbidity
6 months
Lipid levels
Periodo de tiempo: 12 months
Lipid levels in assessing metabolic comorbidity
12 months
Liver enzymes levels
Periodo de tiempo: Baseline
Liver enzymes levels for ALT, AST, and ALP
Baseline
Liver enzymes levels
Periodo de tiempo: 6 months
Liver enzymes levels for ALT, AST, and ALP
6 months
Liver enzymes levels
Periodo de tiempo: 12 months
Liver enzymes levels for ALT, AST, and ALP
12 months
Bilirubin level
Periodo de tiempo: Baseline
Liver enzyme level for Bilirubin
Baseline
Bilirubin level
Periodo de tiempo: 6 months
Liver enzyme level for Bilirubin
6 months
Bilirubin level
Periodo de tiempo: 12 months
Liver enzyme level for Bilirubin
12 months

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Amreen Dinani, Icahn School of Medicine, Division of Liver Diseases

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)

3 de octubre de 2018

Finalización primaria (Actual)

31 de octubre de 2019

Finalización del estudio (Actual)

31 de octubre de 2019

Fechas de registro del estudio

Enviado por primera vez

28 de julio de 2021

Primero enviado que cumplió con los criterios de control de calidad

28 de julio de 2021

Publicado por primera vez (Actual)

3 de agosto de 2021

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

3 de agosto de 2021

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

28 de julio de 2021

Última verificación

1 de julio de 2021

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • GCO 18-1283

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

No

Descripción del plan IPD

was not including inn protocol and consent form

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

producto fabricado y exportado desde los EE. UU.

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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