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Nonalcoholic Fatty Liver DiseaseNCT04988204

Diabetes Prevention Program for the Treatment of Nonalcoholic Fatty Liver Disease

A study testing Diabetes Prevention Program in people with Nonalcoholic Fatty Liver Disease, run by Icahn School of Medicine at Mount Sinai at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Nonalcoholic Fatty Liver Disease
What is being tested?
Diabetes Prevention Program
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
1 siteUnited States
Study dates
3 Oct 2018to 31 Oct 2019
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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.

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Mount Sinai Union Square

    New York, New York, 10003

Other trials in United States

About this study

Official title: 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.

Read more

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.

Being tested
Diabetes Prevention Program
Medical subject headings
Non-alcoholic Fatty Liver Disease

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Diabetes Prevention ProgramBehavioural

    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.

Study groups in NCT04988204
Study groupRoleWhat they receive
Treatment ArmExperimentalPatients enrolled in 1 year program
Receives: Behavioral: Diabetes Prevention Program

What is being measured

The primary outcome is the main question the study is designed to answer.

  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

    Measured: 12 months

Secondary outcomes (16)
  1. Change in Weight

    Change in Weight at 12 months as compared to baseline

    Measured: baseline and 12 months

  2. Hepatic steatosis via Fibroscan

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

    Measured: Baseline

  3. Hepatic steatosis via Fibroscan

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

    Measured: 6 months

  4. Hepatic steatosis via Fibroscan

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

    Measured: 12 months

  5. Glycosylated A1C

    Glycosylated A1C in assessing metabolic comorbidity

    Measured: Baseline

  6. Glycosylated A1C

    Glycosylated A1C in assessing metabolic comorbidity

    Measured: 6 months

  7. Glycosylated A1C

    Glycosylated A1C in assessing metabolic comorbidity

    Measured: 12 months

  8. Lipid levels

    Lipid levels in assessing metabolic comorbidity

    Measured: Baseline

  9. Lipid levels

    Lipid levels in assessing metabolic comorbidity

    Measured: 6 months

  10. Lipid levels

    Lipid levels in assessing metabolic comorbidity

    Measured: 12 months

  11. Liver enzymes levels

    Liver enzymes levels for ALT, AST, and ALP

    Measured: Baseline

  12. Liver enzymes levels

    Liver enzymes levels for ALT, AST, and ALP

    Measured: 6 months

  13. Liver enzymes levels

    Liver enzymes levels for ALT, AST, and ALP

    Measured: 12 months

  14. Bilirubin level

    Liver enzyme level for Bilirubin

    Measured: Baseline

  15. Bilirubin level

    Liver enzyme level for Bilirubin

    Measured: 6 months

  16. Bilirubin level

    Liver enzyme level for Bilirubin

    Measured: 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Aug 2021
  2. Study start3 Oct 2018
  3. Primary completion31 Oct 2019
  4. Study completion31 Oct 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
20 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04988204
Sponsor's protocol ID
GCO 18-1283
Status last verified
Jul 2021
First submitted
28 Jul 2021
Last updated
3 Aug 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: was not including inn protocol and consent form

Publications

  • Hershman M, Torbjornsen K, Pang D, Wyatt B, Dieterich DT, Perumalswami PV, Branch AD, Dinani AM. Modification of the diabetes prevention program for the treatment of nonalcoholic fatty liver disease: A pilot study. Obes Sci Pract. 2022 Oct 20;9(3):218-225. doi: 10.1002/osp4.637. eCollection 2023 Jun.

    PubMed 37287520

Questions about this trial

What is this clinical trial studying?

A study testing Diabetes Prevention Program in people with Nonalcoholic Fatty Liver Disease, run by Icahn School of Medicine at Mount Sinai at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 3 Aug 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of participants in the program at the end of the study (time frame: 12 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04988204, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Aug 2021.

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