Non-Alcoholic Fatty Liver Disease. K76.0
Conditions
Interventions
Intervention 1: Intervention group: Educational sessions emphasizing empowering patients to have healthy nutrition and increase physical activity. To the intervention group, booklet, pamphlet, physica
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 50 Years
Inclusion criteria
Inclusion criteria: Patients with non-alcoholic fatty liver, according to ultrasound diagnosis and approved by physician. Patients with non-alcoholic fatty liver, which according to their physician's diagnosis do not need to receive Livergol. The age of the participants is between 20-50 years. Participants will have at least a degree of reading and writing literacy. Participants are resident in Lar. Interested in participating in the study. Interested in attending training sessions. Failure to develop diseases that cause fatty liver, such as: Hepatitis C, Ray Syndrome, HELLP Syndrome. No drug use: Mipomersen, Lumitapid, Amiodarone, Methotrexate, Tamoxifen, Corticosteroids, Valproic acid drugs, Antiretroviral drugs. No alcohol use.
Exclusion criteria
Exclusion criteria: Absence in more than one training session. Participant withdrawal for participation in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changing nutritional behavior towards healthy eating. Timepoint: Before the intervention, one week and three months after the intervention. Method of measurement: questionnaire.;Change in physical activity to increase physical activity. Timepoint: Before the intervention, one week and three months after the intervention. Method of measurement: questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNarges Mobasheri
Shiraz University of Medical Sciences
Outcome results
None listed