The effect of eight weeks resistance training along with green coffee supplementation in obese women

The effect of eight weeks elastic bands resistance training along with green coffee supplementation on lipid profiles and atherogenic index of plasma in obese women

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2017090419995N9

Enrollment

Registered

2017-10-04

Start date

2017-04-09

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

Obesity. Obesity due to excess calories

Interventions

Intervention 1: Intervention group 1: Subjects in green coffee supplementation group receive 400 mg capsules containing green coffee extract daily for 8 weeks. Intervention 2: Intervention group 2: Re

Treatment - Drugs

Placebo

Intervention group 1: Subjects in green coffee supplementation group receive 400 mg capsules containing green coffee extract daily for 8 weeks.

Intervention group 2: Resistance band training with green coffee group, Subjects in this group in addition to received 400 mg capsules containing green coffee extract daily, elastic band training will

Intervention group 3: Resistance band training group, in this group will be performed elastic band training three sessions a week in eight week. In each session of Resistance band training are perform

Control group: The control group consume one daily capsule containing roasted wheat flour with the same appearance as the original supplement (as placebo).

Eligibility

Sex/Gender

Female

Age

30 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: female; age between 30 to 50 years old; obesity (BMI>30); green coffee insensitivity; the level of physical and mental health. Exclusion criteria: history of cardiovascular diseases; cancer; diabetes; kidney and liver disease; weight-loss dietary adherence; weight changes over 5 kg in the last three months; irregular menstrual cycle.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Lipid profiles (TG, TC, HDL-C and LDL-C). Timepoint: Before and after 8 weeks of intervention. Method of measurement: Blood samples.;Atherogenic Index (AIP). Timepoint: Before and after 8 weeks of intervention. Method of measurement: the logarithmic equation of TG to HDL-C ratio.	—

Secondary

Measure	Time frame
Body fat percent. Timepoint: Before and after 8 weeks of intervention. Method of measurement: Use the Harpenden model calipers.;Body Mass Index (BMI). Timepoint: Before and after 8 weeks of intervention. Method of measurement: Weight divided by height squared.;Weight. Timepoint: Before and after 8 weeks of intervention. Method of measurement: Weight meter.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Tina Jafari

Shahrekord University of Medical Sciences

Tinajafari15@yahoo.com+98 38 3333 4911

Outcome results

None listed

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