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Comparing the Effects of Multicomponent Exercise on Cardiovascular Health and Lipid Profiles in Premenopausal and Postmenopausal Women

U

University of Évora

Status

Completed

Conditions

Menopause
Cardiovascular

Treatments

Other: Experimental: Pre-Menopausic
Other: Experimental: Post- Menopausic

Study type

Interventional

Funder types

Other

Identifiers

NCT06802484
22137 (Other Identifier)

Details and patient eligibility

About

Background: The present study aimed to examine the effects of a 26-week multicomponent exercise program on lipid and lipoprotein profiles, blood pressure, and anthropometric parameters in healthy but sedentary premenopausal and postmenopausal women aged 40-60.

Method: The program, comprising resistance, balance, flexibility, and aerobic exercises, aimed to identify group-specific responses and establish the program's efficacy in mitigating cardiovascular risks. Seventy-five women were recruited, and 38 completed the intervention. Participants were categorized into premenopausal (n=18), postmenopausal (n=10), and control groups (n=10). Key measures included total cholesterol, low- and high-density lipoprotein cholesterol, triglycerides, glucose, systolic and diastolic blood pressure, and anthropometric variables. Statistical analyses employed the Shapiro-Wilk test, paired t-tests, Wilcoxon tests, and Kruskal-Wallis tests, with α=0.05.

Enrollment

75 patients

Sex

Female

Ages

40 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • women aged between 40 and 60 years old;
  • healthy, asymptomatic, and non-smoking;
  • medical diagnosis favouring the engagement in physical-sporting activities;
  • absence of clinical history related to alcoholism or uncontrolled metabolic disease;
  • no clinical prescription for hypotensive pharmacological intake, cholesterol reduction, hormonal replacement therapy, or any other intervention capable of inducing alterations in lipid and lipoprotein metabolism; or
  • abnormal blood sample results.

Exclusion criteria

  • non-fulfilment of inclusion criteria;
  • clinical history characterized by symptoms related to cardiovascular disease (CVD), including stroke (CVA) and coronary vascular disease (CVD), renal or hepatic disease, musculoskeletal disorders, or rheumatoid conditions that may impede full participation in the exercise program.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

75 participants in 3 patient groups

Control
No Intervention group
Pre-Menopausic
Experimental group
Treatment:
Other: Experimental: Pre-Menopausic
Post- Menopausic
Experimental group
Treatment:
Other: Experimental: Post- Menopausic

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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