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Effects of CE on the Risk of Arteriosclerosis in SED Postmenopausal Women

Effects of Combined Exercise on the Risk of Arteriosclerosis in Sedentary Postmenopausal Women

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07550829
Enrollment
113
Registered
2026-04-24
Start date
2025-02-15
Completion date
2025-12-30
Last updated
2026-04-24

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

Conditions

Sedentary

Keywords

Combined exercise, Arteriosclerosis, Sedentary, Postmenopausal women

Brief summary

This study investigated the effects of three exercise modalities: aerobic exercise, resistance exercise, and combined exercise on the risk of arteriosclerosis in sedentary postmenopausal women.

Detailed description

This study aims to compare the effects of different kinds of exercise on the risk of arteriosclerosis in sedentary postmenopausal women. Participants were recruited and randomly assigned to aerobic exercise, resistance exercise, combined exercise or control group. The intervention lasted for 12 weeks. Endothelial function indicators, chronic inflammation indicators, arteriosclerosis related indicators, blood pressure indicators were assessed before and after the intervention.

Interventions

BEHAVIORALAE group

Aerobic exercise

BEHAVIORALRE group

Resistance exercise

BEHAVIORALCE group

Combined exercise

BEHAVIORALON group

No intervention

Sponsors

Beijing Sport University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
45 Years to 69 Years
Healthy volunteers
Yes

Inclusion criteria

* Participants have been postmenopausal for more than 12 months and have not received any exogenous estrogen supplementation after menopause. * Participants were screened using the International Physical Activity Questionnaire-Short Form (IPAQ-S), with a physical activity level classified as "low." They must not have engaged in moderate-intensity physical activity for at least 3 days per week, with a duration of no less than 30 minutes per day, for over 3 consecutive months. * Participants were screened using the Physical Activity Readiness Questionnaire+ (PAR-Q+) and be deemed safe to undergo further intervention.

Exclusion criteria

* Participants with acute or chronic musculoskeletal disorders, cardiovascular diseases, or similar conditions. * Participants with abnormal blood pressure: resting systolic blood pressure \>140 mmHg or diastolic blood pressure \>90 mmHg, or those taking antihypertensive medications. * Participants with abnormally high arterial stiffness (within pathological range): brachial-ankle pulse wave velocity (baPWV) \>1800 cm/s. * Participants recently taken medications that may affect blood indicators, such as hormones or anti-inflammatory drugs. * Participants with unstable body weight in the past 3 months (fluctuation greater than ±2.5 kg). * Participants currently participating in other intervention studies or those with regular exercise habits in daily life. * Participants who smoke or consume alcohol regularly.

Design outcomes

Primary

MeasureTime frameDescription
Flow mediated dilation (FMD)12 weeksThe change of flow mediated dilation before and after intervention.
Brachial ankle pulse wave velocity (baPWV)12 weeksThe change of baPWV before and after intervention.
Ankle brachial index (ABI)12 weeksThe change of ABI before and after intervention.
Carotid intima-media thickness (cIMT)12 weeksThe change of cIMT before and after intervention.
Systolic blood pressure (SBP)12 weeksThe change of SBP before and after intervention.
Diastolic blood pressure (DBP)12 weeksThe change of DBP before and after intervention.
Peak systolic velocity (PSV)12 weeksThe change of PSV of carotid artery before and after intervention.
End diastolic velocity (EDV)12 weeksThe change of EDV of carotid artery before and after intervention.
Pulsatility index (PI)12 weeksThe change of PI of carotid artery before and after intervention.
Resistance index (RI)12 weeksThe change of RI of carotid artery before and after intervention.
Wall Shear Stress (WSS)12 weeksThe change of WSS of carotid artery before and after intervention.

Secondary

MeasureTime frameDescription
Nitric oxide (NO)12 weeksThe change of serum NO before and after intervention.
Prostacyclin (PGI2)12 weeksThe change of serum PGI2 before and after intervention.
Endothelin-1 (ET-1)12 weeksThe change of serum ET-1 before and after intervention.
Angiotensin II (AngII)12 weeksThe change of serum AngII before and after intervention.
C-Reactive protein (CRP)12 weeksThe change of serum CRP before and after intervention.
Interleukin-6 (IL-6)12 weeksThe change of serum IL-6 before and after intervention.
Estrogen12 weeksThe change of serum estrogen before and after intervention.
Soluble intercellular adhesion molecule-1(sICAM-1)12 weeksThe change of serum sICAM-1 before and after intervention.
Soluble vascular cell adhesion molecule-1 (sVCAM-1)12 weeksThe change of serum sVCAM-1 before and after intervention.
Total Cholesterol (TC)12 weeksThe change of serum TC before and after intervention.
High-density lipoprotein cholesterol (HDL-C)12 weeksThe change of serum HDL-C before and after intervention.
Low-density lipoprotein cholesterol (LDL-C)12 weeksThe change of serum LDL-C before and after intervention.
Left ventricular posterior wall thickness at end-diastole (LVPWd)12 weeksThe change of LVPWd before and after intervention.
Left ventricular posterior wall thickness at end-systole (LVPWs)12 weeksThe change of LVPWs before and after intervention.
Stroke volume (SV)12 weeksThe change of SV before and after intervention.
Heart rate (HR)12 weeksThe change of HR before and after intervention.
Left ventricular ejection fraction (LVEF)12 weeksThe change of LVEF before and after intervention.
Cardiac output (CO)12 weeksThe change of CO before and after intervention.
Endothelial Nitric Oxide Synthase (eNOS)12 weeksThe change of serum eNOS before and after intervention.
Maximal oxygen uptake (VO2max)12 weeksThe change of VO2max before and after intervention.
Body mass index (BMI)12 weeksThe change of BMI before and after intervention.
Body fat weight12 weeksThe change of body fat weight before and after intervention.
Body fat%12 weeksThe change of body fat% before and after intervention.
Pittsburgh sleep quality index (PSQI)12 weeksThe change of PSQI before and after intervention.
Food frequency questionnaire (FFQ)12 weeksThe change of FFQ before and after intervention.
Cluster of Differentiation 14 (CD14) mRNA and Protein Expression12 weeksThe change of CD14 mRNA and Protein Expression before and after intervention.
Mitogen-activated protein kinase 14 (MAPK14) mRNA12 weeksThe change of MAPK14 mRNA before and after intervention.
p38 Mitogen-activated protein kinase (p38 MAPK) Protein Expression12 weeksThe change of p38 MAPK Protein Expression before and after intervention.
Tetraspanin 4 (TSPAN4) mRNA and Protein Expression12 weeksThe change of TSPAN4 mRNA and Protein Expression before and after intervention.
Nitric Oxide Synthase 3 (NOS3) mRNA and Protein Expression12 weeksThe change of NOS3 mRNA and Protein Expression before and after intervention.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 25, 2026