Selected Pilates training on lipid profile, fasting blood sugar, blood pressure and fat percentage of women with non-alcoholic fatty liver disease

Response of eight weeks of selected Pilates training on lipid profile, fasting blood sugar, blood pressure and fat percentage of women with non-alcoholic fatty liver disease in Ahvaz city

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230216057435N2

Enrollment

Registered

2023-12-23

Start date

2023-05-20

Completion date

Unknown

Last updated

2024-01-22

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

Conditions

Non-alcoholic fatty liver disease. Fatty (change of) liver, not elsewhere classified. (Nonalcoholic fatty liver disease [NAFLD])

Interventions

Intervention 1: Intervention group: Pilates group performed performed 60 minutes(10 min warm-up, 40 min Pilates training, and 10 min cool-down) of Mat Pilates training three days a week for eight week

Eligibility

Sex/Gender

Female

Age

30 Years to 55 Years

Inclusion criteria

Inclusion criteria: Women with non-alcoholic fatty liver disease Age range from 30 to 55 years Not suffering from cardiovascular, joint and skeletal diseases Not performing regular sports activities during the last 6 months

Exclusion criteria

Exclusion criteria: Taking supplements or lipid-lowering medication

Design outcomes

Primary

Measure	Time frame
Lipid profile. Timepoint: 24hours before and 48 hours after the end of the protocol. Method of measurement: Laboratory test kits.;Fasting blood sugar. Timepoint: 24hours before and 48 hours after the end of the protocol. Method of measurement: Laboratory test kits.;Blood pressure. Timepoint: 24hours before and 48 hours after the end of the protocol. Method of measurement: Automatic Blood Pressure.;Fat percentage. Timepoint: 24hours before and 48 hours after the end of the protocol. Method of measurement: Harpenden calipers.	—

Measure

Time frame

Lipid profile. Timepoint: 24hours before and 48 hours after the end of the protocol. Method of measurement: Laboratory test kits.;Fasting blood sugar. Timepoint: 24hours before and 48 hours after the end of the protocol. Method of measurement: Laboratory test kits.;Blood pressure. Timepoint: 24hours before and 48 hours after the end of the protocol. Method of measurement: Automatic Blood Pressure.;Fat percentage. Timepoint: 24hours before and 48 hours after the end of the protocol. Method of measurement: Harpenden calipers.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSedigheh Kaabomeir

Shahid Chamran University of Ahvaz

s.kaabomeir1996@gmail.com+98 916 090 4022

Outcome results

None listed

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