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12 Weeks of Resistance Band Exercise Impacts on Metabolic Syndrome Progression in Postmenopausal Women

Impacts of 12 Weeks of Resistance Band Exercise Training on Insulin Resistance, Blood Lipids, Body Composition, and Blood Pressure in Postmenopausal Women With Obesity

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04014686
Enrollment
36
Registered
2019-07-10
Start date
2018-04-01
Completion date
2018-10-01
Last updated
2020-11-03

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

Conditions

Dyslipidemias, Hypertension, Insulin Resistance, Metabolic Syndrome

Keywords

postmenopausal, exercise

Brief summary

The purpose of this study was to examine the impacts of a 12-week resistance band exercise program on insulin resistance, blood lipid profiles, body composition, and blood pressure in postmenopausal women with obesity. Thirty-six postmenopausal women participated in this study. Participants were randomly allocated into the resistance band training group (EX, n = 18) or the control group (CON, n = 18). The EX group performed a resistance band exercise training program 60 minutes per day, 3 times per week, for 12 weeks. The CON group did not participate in any exercise, dietary, or behavioral intervention. Blood glucose, insulin, homeostatic model of insulin resistance (HOMA-IR), blood lipids, blood pressure, and body composition were measured before and after 12 weeks of EX or CON.

Interventions

no exercise intervention

BEHAVIORALResistance band exercise intervention group

Resistance band exercise training intervention (12 weeks, 3x per week, for 60 minutes per day)

Sponsors

Dong-Eui University
CollaboratorOTHER
University of Nebraska
CollaboratorOTHER
Pusan National University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

exercise intervention group, control group

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* postmenopausal (cessation of menses for at least 12 consecutive months) * abdominal obesity (waist \> 80 cm)

Exclusion criteria

* current smoker (smoking within 6 months of participation) * cardiovascular disease * renal disease * pulmonary disease * thyroid disease

Design outcomes

Primary

MeasureTime frameDescription
Glucose12 weeksBlood glucose was measured before and after 12 weeks.
Insulin12 weeksBlood insulin was measured before and after 12 weeks.
Percentage of Body Fat12 weeksBody fat percentage was measured before and after 12 weeks.
Waist circumference12 weeksWaist circumference was measured before and after 12 weeks.

Secondary

MeasureTime frameDescription
Systolic blood pressure12 weeksSystolic blood pressure was measured before and after 12 weeks.
Diastolic blood pressure12 weeksDiastolic blood pressure was measured before and after 12 weeks.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026