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NASH Fitness Intervention in Thrombosis Trial (NASHFit)

NASH Fitness Intervention in Thrombosis Trial (NASHFit)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03518294
Enrollment
28
Registered
2018-05-08
Start date
2018-06-01
Completion date
2021-03-24
Last updated
2023-02-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blood Disorder, Digestive System Disease, Liver Diseases

Keywords

NAFLD, NASH

Brief summary

Nonalcoholic fatty liver disease (NAFLD) is the leading cause of chronic liver disease in the United States. The most advanced forms of NAFLD are associated with increased liver-related mortality and lower overall survival. The current standard of care for NAFLD is lifestyle changes through diet and exercise. The human genome and regulation of gene expression is influenced by physical activity. NAFLD is a prothrombotic state with derangements in all three phases of hemostasis leading to clinically important clotting events. Exercise can improve coagulation in healthy persons. In this proposal, we seek to begin a line of work to answer the question Can lifestyle changes effectively mitigate the increased risk of clotting in patients with NAFLD? focusing initially on the at-risk population genetically susceptible to advanced disease.

Detailed description

Often comorbid with obesity, nonalcoholic fatty liver disease (NAFLD) is the leading cause of chronic liver disease in the United States affecting 75-100 million adults, of which 15-20 million have the more severe variant nonalcoholic steatohepatitis (NASH). Conservative estimates project a doubling in NASH by 2025.The most advanced forms of NAFLD are associated with increased liver-related mortality and lower overall survival. The most effective treatment for NAFLD remains adopting healthy dietary and exercise patterns, however NAFLD patients are among the least physically active individuals. Predicting exercise behavior on an individual level is highly complex due to differing motivation, physiologic response to and subjective experience of exercise as well as emerging genetic evidence. The human genome and regulation of gene expression is influenced by physical activity. Patatin like phospholipase-3 (PNPLA3) rs738409 polymorphism (GG, GC and CC genotypes) plays a crucial role in the development of NAFLD. The GG genotype is both associated with advanced NAFLD, and predicts response to physical activity. Patients with NASH have extensive extrahepatic disease and are hypercoagulable. NASH is a prothrombotic state with fibrinolytic dysfunction through elevated plasminogen activator inhibitor (PAI-1), an independent risk factor for venous thromboembolism (VTE). Consequently, patients with NASH are predisposed to VTE; the risk of portal vein thrombosis (PVT) in NASH is 210% greater than in other liver disease. NASH patients are also at increased risk for pulmonary embolism (PE) and deep vein thrombosis (DVT).The most advanced forms of NASH have the greatest thrombotic risk. While studies observe that change in diet, weight and physical activity patterns improve NASH, it is not clear whether these lifestyle changes also reduce the elevated clot risk, however, moderate-intensity exercise leads to improved fibrinolysis in healthy persons.The NASHFit study is being done to find out if exercise is beneficial in decreasing the risk of clotting problems in patients with NASH. Exercise has been shown to decrease markers of clotting in healthy individuals as well as in those with cardiovascular disease.

Interventions

BEHAVIORALAerobic Exercise

Subjects in the aerobic exercise group will be supervised to exercise 30 minutes, 5 times per week at a moderate intensity. Formal exercise instruction and supervision will be provided by ACSM certified fitness professionals at the Penn State University Fitness Center. Aerobic exercise can be completed on either the treadmill, exercise bike, rowing machine or the elliptical machine.

Sponsors

Milton S. Hershey Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Standard of care Aerobic exercise

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

Adults age \>=18 or \<70 years Liver biopsy \<= 6months prior to enrollment Biopsy proven NASH(79) Lack of secondary causes of hepatic fat accumulation: Significant alcohol consumption (\<21 drinks/week for men and \<14 drinks/week for women) Chronic hepatitis C Wilson disease Lipodystrophy Parenteral nutrition Long-term use of steatogenic medications (mipomersen, lomitapide, amiodarone, methotrexate, tamoxifen, corticosteroids) Monogenic hereditary disorders

Exclusion criteria

\>90 minutes/week of at least moderate intensity exercise over the previous three months Pregnancy BMI \<18 or \>40 kg/m2(16) Uncontrolled diabetes (changes in medication dosing over the previous three months or hemoglobin A1c \>9%)(12) Active cardiac symptoms Severe medical comorbidities/psychiatric illness Decompensated cirrhosis (history of esophageal varices, ascites or hepatic encephalopathy) Abdominal hernia Cancer with life expectancy \<6 months MRI contraindications (severe claustrophobia, implanted ferrous metal) Other liver disease (positive hepatitis B surface antigen, antinuclear antibody titer \>1:160) Active weight-loss program participation or weight-loss supplement use Active substance abuse/smoking Inability to provide informed consent Institutionalized/prisoner Inability to walk \> 2 blocks or ¼ mile. Physical Activity Readiness Questionnaire (PAR-Q) score \>=1 at the discretion of the study PI

Design outcomes

Primary

MeasureTime frameDescription
PAI-1 Level5 monthsChange in fibrinolysis as indicated by PAI-1 level was calculated by taking the difference of measurements at baseline and 5 months.

Secondary

MeasureTime frameDescription
Change in Protein S5 monthsChange in protein S was calculated by taking the difference of measurements at baseline and 5 months.
Change in Factor VIII5 monthsChange in factor VIII was calculated by taking the difference of measurements at baseline and 5 months.
Change in Fibrinogen5 monthsChange in fibrinogen was calculated by taking the difference of measurements at baseline and 5 months.
Change in Antithrombin5 monthsChange in antithrombin was calculated by taking the difference of measurements at baseline and 5 months.
Change in Protein C5 monthsChange in protein C was calculated by taking the difference of measurements at baseline and 5 months.
Change in Von Williebrand Factor (vWF)5 monthsChange in vWF was calculated by taking the difference of measurements at baseline and 5 months.
Patatin Like Phospholipase-3 (PNPLA3) rs738409 Polymorphism5 monthsPatatin like phospholipase-3 (PNPLA3) rs738409 polymorphism genotyping subjects (GG, GC and CC genotypes)
Change in PAI-1 Stratified by Fibrosis Stage5 monthsChange is the difference between measurements at baseline and 5 months
Change in % Hepatic Fat5 monthsChange in % hepatic fat was calculated by taking the difference of measurements at baseline and 5 months.
Health Related Quality of Life (HRQOL) Change5 months (20 weeks)Data was collected at baseline and at 5 months to assess changes in domains of health. PROMIS-29 Profile v2.1 (Physical function & pain interference) PROMIS Bank v2.0 - Instrumental Support (Social Support) Scores are reported as standardized T-score metrics derived from population means, with a mean of 50 and standard deviation of 10. The minimum is 0 and the maximum is 90. A higher score for fatigue, pain intensity, pain interference, sleep disturbance, anxiety and depression means a worse outcome. A higher score for physical function and social roles means a better outcome.
Change in Adiponectin5 monthsChange in adipontin was calculated by taking the difference of measurements at baseline and 5 months.

Countries

United States

Participant flow

Pre-assignment details

31 patients were screened for this study. Three were excluded after screening (two declined and one was excluded because they were actively smoking)

Participants by arm

ArmCount
Standard of Care
Subjects in the control condition will be instructed to continue their medical care at the discretion of their treating medical professional. They will be informed to maintain their current physical activity level. Weekly phone calls will be performed by study personnel to ensure adherence to the protocol (no changes in activity). Subjects will report to Penn State on a monthly basis for anthropometric assessment to confirm their self-reports and study investigators will perform and interim history and physical examination at that time.
10
Aerobic Exercise
Subjects in the aerobic exercise group will be supervised to exercise 30 minutes, 5 times per week at a moderate intensity. Formal exercise instruction and supervision will be provided by ACSM certified fitness professionals at the Penn State University Fitness Center. Aerobic exercise can be completed on either the treadmill, exercise bike, rowing machine or the elliptical machine. Aerobic Exercise: Subjects in the aerobic exercise group will be supervised to exercise 30 minutes, 5 times per week at a moderate intensity. Formal exercise instruction and supervision will be provided by ACSM certified fitness professionals at the Penn State University Fitness Center. Aerobic exercise can be completed on either the treadmill, exercise bike, rowing machine or the elliptical machine.
18
Total28

Baseline characteristics

CharacteristicStandard of CareAerobic ExerciseTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
10 Participants18 Participants28 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
1 Participants1 Participants2 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
9 Participants17 Participants26 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
0 Participants0 Participants0 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
1 Participants0 Participants1 Participants
Race (NIH/OMB)
White
9 Participants18 Participants27 Participants
Region of Enrollment
United States
10 participants18 participants28 participants
Sex: Female, Male
Female
5 Participants6 Participants11 Participants
Sex: Female, Male
Male
5 Participants12 Participants17 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 100 / 18
other
Total, other adverse events
1 / 106 / 18
serious
Total, serious adverse events
1 / 100 / 18

Outcome results

Primary

PAI-1 Level

Change in fibrinolysis as indicated by PAI-1 level was calculated by taking the difference of measurements at baseline and 5 months.

Time frame: 5 months

ArmMeasureValue (MEAN)Dispersion
Standard of CarePAI-1 Level151.4 ng/mLStandard Deviation 51.5
Aerobic ExercisePAI-1 Level176.2 ng/mLStandard Deviation 71.9
Secondary

Change in Adiponectin

Change in adipontin was calculated by taking the difference of measurements at baseline and 5 months.

Time frame: 5 months

ArmMeasureValue (MEAN)Dispersion
Standard of CareChange in Adiponectin3482.3 ng/mLStandard Deviation 1728.8
Aerobic ExerciseChange in Adiponectin1065.1 ng/mLStandard Deviation 1220.7
Secondary

Change in Antithrombin

Change in antithrombin was calculated by taking the difference of measurements at baseline and 5 months.

Time frame: 5 months

ArmMeasureValue (MEAN)Dispersion
Standard of CareChange in Antithrombin95.6 percentage of proteinStandard Deviation 12.1
Aerobic ExerciseChange in Antithrombin102.2 percentage of proteinStandard Deviation 15.6
Secondary

Change in Factor VIII

Change in factor VIII was calculated by taking the difference of measurements at baseline and 5 months.

Time frame: 5 months

ArmMeasureValue (MEAN)Dispersion
Standard of CareChange in Factor VIII210.0 International Units/LiterStandard Deviation 75
Aerobic ExerciseChange in Factor VIII188.6 International Units/LiterStandard Deviation 66.4
Secondary

Change in Fibrinogen

Change in fibrinogen was calculated by taking the difference of measurements at baseline and 5 months.

Time frame: 5 months

ArmMeasureValue (MEAN)Dispersion
Standard of CareChange in Fibrinogen352.4 mg/dLStandard Deviation 56.1
Aerobic ExerciseChange in Fibrinogen377.2 mg/dLStandard Deviation 83.5
Secondary

Change in % Hepatic Fat

Change in % hepatic fat was calculated by taking the difference of measurements at baseline and 5 months.

Time frame: 5 months

ArmMeasureValue (MEAN)Dispersion
Standard of CareChange in % Hepatic Fat22.5 percentage of liverStandard Deviation 10.5
Aerobic ExerciseChange in % Hepatic Fat20.4 percentage of liverStandard Deviation 7.7
Secondary

Change in PAI-1 Stratified by Fibrosis Stage

Change is the difference between measurements at baseline and 5 months

Time frame: 5 months

Population: The intended analysis was not performed for both groups, and instead this subset analyzed exercise group participants only.

ArmMeasureGroupValue (MEAN)Dispersion
Standard of CareChange in PAI-1 Stratified by Fibrosis StageBaseline176.7 ng/mLStandard Deviation 120.9
Standard of CareChange in PAI-1 Stratified by Fibrosis StagePost exercise122.7 ng/mLStandard Deviation 36.6
Aerobic ExerciseChange in PAI-1 Stratified by Fibrosis StageBaseline241.4 ng/mLStandard Deviation 4.8
Aerobic ExerciseChange in PAI-1 Stratified by Fibrosis StagePost exercise196.1 ng/mLStandard Deviation 46.5
F3 FibrosisChange in PAI-1 Stratified by Fibrosis StagePost exercise127.8 ng/mLStandard Deviation 36.7
F3 FibrosisChange in PAI-1 Stratified by Fibrosis StageBaseline131.7 ng/mLStandard Deviation 24.4
Secondary

Change in Protein C

Change in protein C was calculated by taking the difference of measurements at baseline and 5 months.

Time frame: 5 months

ArmMeasureValue (MEAN)Dispersion
Standard of CareChange in Protein C169.0 IU/dLStandard Deviation 50.6
Aerobic ExerciseChange in Protein C152.6 IU/dLStandard Deviation 55.9
Secondary

Change in Protein S

Change in protein S was calculated by taking the difference of measurements at baseline and 5 months.

Time frame: 5 months

ArmMeasureValue (MEAN)Dispersion
Standard of CareChange in Protein S106.3 IU/dLStandard Deviation 24.6
Aerobic ExerciseChange in Protein S101.5 IU/dLStandard Deviation 22.4
Secondary

Change in Von Williebrand Factor (vWF)

Change in vWF was calculated by taking the difference of measurements at baseline and 5 months.

Time frame: 5 months

ArmMeasureValue (MEAN)Dispersion
Standard of CareChange in Von Williebrand Factor (vWF)140.1 International Units/LiterStandard Deviation 63.1
Aerobic ExerciseChange in Von Williebrand Factor (vWF)128.4 International Units/LiterStandard Deviation 39.8
Secondary

Health Related Quality of Life (HRQOL) Change

Data was collected at baseline and at 5 months to assess changes in domains of health. PROMIS-29 Profile v2.1 (Physical function & pain interference) PROMIS Bank v2.0 - Instrumental Support (Social Support) Scores are reported as standardized T-score metrics derived from population means, with a mean of 50 and standard deviation of 10. The minimum is 0 and the maximum is 90. A higher score for fatigue, pain intensity, pain interference, sleep disturbance, anxiety and depression means a worse outcome. A higher score for physical function and social roles means a better outcome.

Time frame: 5 months (20 weeks)

Population: ITT

ArmMeasureGroupValue (MEAN)Dispersion
Standard of CareHealth Related Quality of Life (HRQOL) ChangePhysical function-2.5 T-scoreStandard Deviation 6.5
Standard of CareHealth Related Quality of Life (HRQOL) ChangePain interference4.3 T-scoreStandard Deviation 9.6
Standard of CareHealth Related Quality of Life (HRQOL) ChangeSocial support-0.7 T-scoreStandard Deviation 6.6
Aerobic ExerciseHealth Related Quality of Life (HRQOL) ChangePain interference-3.4 T-scoreStandard Deviation 5.6
Aerobic ExerciseHealth Related Quality of Life (HRQOL) ChangePhysical function1.5 T-scoreStandard Deviation 5
Aerobic ExerciseHealth Related Quality of Life (HRQOL) ChangeSocial support5.0 T-scoreStandard Deviation 7
Secondary

Patatin Like Phospholipase-3 (PNPLA3) rs738409 Polymorphism

Patatin like phospholipase-3 (PNPLA3) rs738409 polymorphism genotyping subjects (GG, GC and CC genotypes)

Time frame: 5 months

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
Standard of CarePatatin Like Phospholipase-3 (PNPLA3) rs738409 PolymorphismCC3 Participants
Standard of CarePatatin Like Phospholipase-3 (PNPLA3) rs738409 PolymorphismGC5 Participants
Standard of CarePatatin Like Phospholipase-3 (PNPLA3) rs738409 PolymorphismGG2 Participants
Aerobic ExercisePatatin Like Phospholipase-3 (PNPLA3) rs738409 PolymorphismCC8 Participants
Aerobic ExercisePatatin Like Phospholipase-3 (PNPLA3) rs738409 PolymorphismGC5 Participants
Aerobic ExercisePatatin Like Phospholipase-3 (PNPLA3) rs738409 PolymorphismGG5 Participants

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026