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The Effectiveness of Two Months of Cyclic Yoga Exercise on Type 2 Diabetes Patients with Non-alcoholic fatty liver disease

The Effectiveness of Two Months of Cyclic Yoga Exercise on Glycemic Indices, Liver Enzymes and Anthropometric Indices in Type 2 Diabetes Patients with Non-alcoholic fatty liver disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110527006611N4
Enrollment
40
Registered
2023-05-17
Start date
2021-06-10
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Condition 1: Type 2 Diabetes. Condition 2: Non-alcoholic fatty liver. Type 2 diabetes mellitus Fatty (change of) liver, not elsewhere classified

Interventions

Intervention 1: Intervention group: Yoga exercise group: This group performed cyclic yoga exercise for two months, three days a week. Cyclic Yoga is the art of sequencing yoga asana, pranayama and mu

Sponsors

Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 55 Years

Inclusion criteria

Inclusion criteria: Type 2 diabetic women with Non-alcoholic fatty liver disease Type 2 diabetic women 45 to 55 years old with overweight

Exclusion criteria

Exclusion criteria: No insulin treatment No complications of diabetes (neuropathy, nephropathy, retinopathy) No use of drugs and alcoholic drinks, Not participating in regular exercise activities No history of cardiovascular and mental illness No history of fractures, surgery or joint diseases, Three times or more Absence in training sessions Lack of hormone therapy

Design outcomes

Primary

MeasureTime frame
Glycosylated Hemoglobin. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with Pishtaz Teb kit.;Fasting blood glucose. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with BioSystems kit.;Fatty liver grade. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Ultrasound.

Secondary

MeasureTime frame
Alanine Aminotransferase enzyme. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with BioSystems kit.;Aspartate Aminotransferase enzyme. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with BioSystems kit.;Alkaline phosphatase enzyme. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with BioSystems kit.;LDL Cholesterol. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with BioSystems kit.;Triglyceride. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with BioSystems kit.;HDL Cholesterol. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with BioSystems kit.;Cholesterol. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with BioSystems kit.;Insulin Hormone. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test Siemens kit made in America.;Waist Circumference. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Standard tape meter.;Blood Pressure. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: brachial digital blood pressure monitor.;IGF-1 Hormone. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with DiaSorin kit

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Bayat

University of Tehran

z.bayat@ut.ac.ir+98 83 3838 3184

Outcome results

None listed

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