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The Effect of Exercise and nutrition on fatty liver disease

The assessment effect of aerobic training program on serum transaminases' levels and quality of life in patients with Non-Alcoholic Steatohepatitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201104286319N1
Enrollment
30
Registered
2011-08-27
Start date
2010-04-04
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Non Alcoholic Steatohepatitis. Diseases of liver

Interventions

Intervention 1: Diet with aerobic training program. Intervention 2: Diet alone.
Treatment - Devices
Treatment - Other
Diet with aerobic training program

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 18 to 65 years ; Approval Kbdchrb ultrasound; Increase 1.5 Equity serum enzyme alanine aminotransferase. Exclusion criteria: Hepatitis B2; Hepatitis C; Autoimmune hepatitis; CD; Wilson; 1a-deficient anti-trypsin; Hemochromatosis; thyroid disease; Ischemic heart disease; kidney failure; Drugs Hpatvtvksyk; More than 20 grams of alcohol per day.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
LDL. Timepoint: Before the intervention, two months after the start and end of three months. Method of measurement: mg/dL.;HDL. Timepoint: Before the intervention, two months after the start and end of three months. Method of measurement: mg/dL.;VLDL. Timepoint: Before the intervention, two months after the start and end of three months. Method of measurement: mg/dL.;TG. Timepoint: Before the intervention, two months after the start and end of three months. Method of measurement: mg/dL.;Weight. Timepoint: Before the intervention, two months after the start and end of three months. Method of measurement: gram.;BMI. Timepoint: Before the intervention, two months after the start and end of three months. Method of measurement: Kg/M2.;ALT. Timepoint: Before the intervention, two months after the start and end of three months. Method of measurement: Unit U / L, a photometer methods.;AST. Timepoint: Before the intervention, two months after the start and end of three months. Method of measurement: Unit U / L, a photometer methods.;FBS. Timepoint: Before the intervention, two months after the start and end of three months. Method of measurement: mg/dL.;Insulin. Timepoint: Before the intervention, two months after the start and end of three months. Method of measurement: mIU/mL.;Chol. Timepoint: Before the intervention, two months after the start and end of three months. Method of measurement: mg/dL.;WC. Timepoint: Before the intervention, two months after the start and end of three months. Method of measurement: Cm.;WHpR. Timepoint: Before the intervention, two months after the start and end of three months. Method of measurement: %.;WHtR. Timepoint: Before the intervention, two months after the start and end of three months. Method of measurement: %.;HC. Timepoint: Before the intervention, two months after the start and end of three months. Method of measurement: Cm.;PBF. Timepoint: Before the intervention, two months after the start and end of three months. Method of meas

Secondary

MeasureTime frame
Height. Timepoint: Before the intervention, two months later and after three months. Method of measurement: Cm.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mohsen Nematy

Mashhad University of Medical Sciences

NematyM@mums.ac.ir+98 51 1882 8569

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026