Diabetes Prevention Program for the Treatment of Nonalcoholic Fatty Liver Disease
Primary Purpose
Nonalcoholic Fatty Liver Disease
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Diabetes Prevention Program
Sponsored by
About this trial
This is an interventional treatment trial for Nonalcoholic Fatty Liver Disease
Eligibility Criteria
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.
Sites / Locations
- Mount Sinai Union Square
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Treatment Arm
Arm Description
Patients enrolled in 1 year program
Outcomes
Primary Outcome Measures
Number of participants in the program at the end of the study
Retention defined as number of patients in the program at the end of the study
Secondary Outcome Measures
Change in Weight
Change in Weight at 12 months as compared to baseline
Hepatic steatosis via Fibroscan
Changes in hepatic steatosis measured with fibroscan using the controlled attenuated parameter.
Hepatic steatosis via Fibroscan
Changes in hepatic steatosis measured with fibroscan using the controlled attenuated parameter .
Hepatic steatosis via Fibroscan
Changes in hepatic steatosis measured with fibroscan using the controlled attenuated parameter.
Glycosylated A1C
Glycosylated A1C in assessing metabolic comorbidity
Glycosylated A1C
Glycosylated A1C in assessing metabolic comorbidity
Glycosylated A1C
Glycosylated A1C in assessing metabolic comorbidity
Lipid levels
Lipid levels in assessing metabolic comorbidity
Lipid levels
Lipid levels in assessing metabolic comorbidity
Lipid levels
Lipid levels in assessing metabolic comorbidity
Liver enzymes levels
Liver enzymes levels for ALT, AST, and ALP
Liver enzymes levels
Liver enzymes levels for ALT, AST, and ALP
Liver enzymes levels
Liver enzymes levels for ALT, AST, and ALP
Bilirubin level
Liver enzyme level for Bilirubin
Bilirubin level
Liver enzyme level for Bilirubin
Bilirubin level
Liver enzyme level for Bilirubin
Full Information
NCT ID
NCT04988204
First Posted
July 28, 2021
Last Updated
July 28, 2021
Sponsor
Icahn School of Medicine at Mount Sinai
1. Study Identification
Unique Protocol Identification Number
NCT04988204
Brief Title
Diabetes Prevention Program for the Treatment of Nonalcoholic Fatty Liver Disease
Official Title
Pilot Study: Diabetes Prevention Program for the Treatment of Nonalcoholic Fatty Liver Disease
Study Type
Interventional
2. Study Status
Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
October 3, 2018 (Actual)
Primary Completion Date
October 31, 2019 (Actual)
Study Completion Date
October 31, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Icahn School of Medicine at Mount Sinai
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nonalcoholic Fatty Liver Disease
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Treatment Arm
Arm Type
Experimental
Arm Description
Patients enrolled in 1 year program
Intervention Type
Behavioral
Intervention Name(s)
Diabetes Prevention Program
Intervention Description
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.
Primary Outcome Measure Information:
Title
Number of participants in the program at the end of the study
Description
Retention defined as number of patients in the program at the end of the study
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Change in Weight
Description
Change in Weight at 12 months as compared to baseline
Time Frame
baseline and 12 months
Title
Hepatic steatosis via Fibroscan
Description
Changes in hepatic steatosis measured with fibroscan using the controlled attenuated parameter.
Time Frame
Baseline
Title
Hepatic steatosis via Fibroscan
Description
Changes in hepatic steatosis measured with fibroscan using the controlled attenuated parameter .
Time Frame
6 months
Title
Hepatic steatosis via Fibroscan
Description
Changes in hepatic steatosis measured with fibroscan using the controlled attenuated parameter.
Time Frame
12 months
Title
Glycosylated A1C
Description
Glycosylated A1C in assessing metabolic comorbidity
Time Frame
Baseline
Title
Glycosylated A1C
Description
Glycosylated A1C in assessing metabolic comorbidity
Time Frame
6 months
Title
Glycosylated A1C
Description
Glycosylated A1C in assessing metabolic comorbidity
Time Frame
12 months
Title
Lipid levels
Description
Lipid levels in assessing metabolic comorbidity
Time Frame
Baseline
Title
Lipid levels
Description
Lipid levels in assessing metabolic comorbidity
Time Frame
6 months
Title
Lipid levels
Description
Lipid levels in assessing metabolic comorbidity
Time Frame
12 months
Title
Liver enzymes levels
Description
Liver enzymes levels for ALT, AST, and ALP
Time Frame
Baseline
Title
Liver enzymes levels
Description
Liver enzymes levels for ALT, AST, and ALP
Time Frame
6 months
Title
Liver enzymes levels
Description
Liver enzymes levels for ALT, AST, and ALP
Time Frame
12 months
Title
Bilirubin level
Description
Liver enzyme level for Bilirubin
Time Frame
Baseline
Title
Bilirubin level
Description
Liver enzyme level for Bilirubin
Time Frame
6 months
Title
Bilirubin level
Description
Liver enzyme level for Bilirubin
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amreen Dinani
Organizational Affiliation
Icahn School of Medicine, Division of Liver Diseases
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mount Sinai Union Square
City
New York
State/Province
New York
ZIP/Postal Code
10003
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
was not including inn protocol and consent form
Learn more about this trial
Diabetes Prevention Program for the Treatment of Nonalcoholic Fatty Liver Disease
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