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CompletedNCT04988204Updated Aug 3, 2021

Diabetes Prevention Program for the Treatment of Nonalcoholic Fatty Liver Disease

An interventional study of Diabetes Prevention Program in Nonalcoholic Fatty Liver Disease, sponsored by Icahn School of Medicine at Mount Sinai. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2021-08-03.

Sponsored by Icahn School of Medicine at Mount Sinai · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years 9 months after the study started (first participant enrolled Oct 2018, registered Jul 2021).
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study 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.

02

Conditions studied

03

In context

Liver Diseases

2,081 studies on the registry are indexed under Liver Diseases; 390 are open to participants now.

This study's enrollment of 20 is below the median of 50 across 1,323 interventional studies indexed under Liver Diseases.

Browse Liver Diseases studies →

Lead sponsor

Icahn School of Medicine at Mount Sinai is the lead sponsor of 764 studies on the registry; 181 are open to participants now.

Of its 121 completed or terminated interventional studies of FDA-regulated products, 82 (68%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (actual)

Study arms

  • Experimental
    Treatment Arm

    Patients enrolled in 1 year program

    Behavioral: Diabetes Prevention Program

Interventions

  • BehavioralDiabetes Prevention 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.

06

What researchers measure

Primary outcomes

  1. 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

    Time frame: 12 months

Secondary outcomes

  1. Change in Weight

    Change in Weight at 12 months as compared to baseline

    Time frame: baseline and 12 months

  2. Hepatic steatosis via Fibroscan

    Changes in hepatic steatosis measured with fibroscan using the controlled attenuated parameter.

    Time frame: Baseline

  3. Hepatic steatosis via Fibroscan

    Changes in hepatic steatosis measured with fibroscan using the controlled attenuated parameter .

    Time frame: 6 months

  4. Hepatic steatosis via Fibroscan

    Changes in hepatic steatosis measured with fibroscan using the controlled attenuated parameter.

    Time frame: 12 months

  5. Glycosylated A1C

    Glycosylated A1C in assessing metabolic comorbidity

    Time frame: Baseline

  6. Glycosylated A1C

    Glycosylated A1C in assessing metabolic comorbidity

    Time frame: 6 months

  7. Glycosylated A1C

    Glycosylated A1C in assessing metabolic comorbidity

    Time frame: 12 months

  8. Lipid levels

    Lipid levels in assessing metabolic comorbidity

    Time frame: Baseline

  9. Lipid levels

    Lipid levels in assessing metabolic comorbidity

    Time frame: 6 months

  10. Lipid levels

    Lipid levels in assessing metabolic comorbidity

    Time frame: 12 months

  11. Liver enzymes levels

    Liver enzymes levels for ALT, AST, and ALP

    Time frame: Baseline

  12. Liver enzymes levels

    Liver enzymes levels for ALT, AST, and ALP

    Time frame: 6 months

  13. Liver enzymes levels

    Liver enzymes levels for ALT, AST, and ALP

    Time frame: 12 months

  14. Bilirubin level

    Liver enzyme level for Bilirubin

    Time frame: Baseline

  15. Bilirubin level

    Liver enzyme level for Bilirubin

    Time frame: 6 months

  16. Bilirubin level

    Liver enzyme level for Bilirubin

    Time frame: 12 months

07

Study locations

1 site
  • Mount Sinai Union Square
    New York, New York 10003, United States
08

References and documents

Individual participant data

Plan to share: No — was not including inn protocol and consent form

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 3, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04988204
Lead sponsor
Icahn School of Medicine at Mount Sinai
Responsible party
Amreen Dinani (Associate Professor, Icahn School of Medicine at Mount Sinai) — Principal investigator
First posted
Aug 3, 2021
Start date
Oct 3, 2018
Primary completion
Oct 31, 2019
Completion
Oct 31, 2019
Last update
Aug 3, 2021

Study contacts

Amreen Dinani
principal investigator · Icahn School of Medicine, Division of Liver Diseases

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2021. You cannot join it, but the record below documents what was studied.

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