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The Influence of Pilates Exercises Training Volume on Metabolic Outcomes in Dyslipidemic Women.

Not Applicable
Completed
Conditions
Dyslipidemias
Interventions
Other: Control Group
Other: High Volume Group
Other: Low Volume Group
Registration Number
NCT03307031
Lead Sponsor
Federal University of Rio Grande do Sul
Brief Summary

The aim of the present study was to assess the influence of different volumes of Pilates training exercises on metabolic, blood pressure (BP), functional physical fitness (PF) and quality of life (QL) outcomes in postmenopausal dyslipidemic women. In total, 26 women participated in the controlled clinical trial, being allocated into three groups: high volume group (HVG; n=9), low volume group (LVG; n=11) and control group (CG, n=6). HVG performed four weekly sessions and LVG performed only twice a week, during 10 weeks with 45 to 55 minutes per session. Before and after the intervention period, metabolic, BP, PF, QL and cardiovascular risk score (CRS) outcomes were measured. The results were described by mean values with lower and upper limits (95% confidence interval). Comparisons between groups and intra-groups were performed adopting Generalized Estimating Equations (GEE) method, with post hoc of Bonferroni and significance level of ɑ=0,05.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
26
Inclusion Criteria
  • Dyslipidemic, postmenopausal and sedentary.
Exclusion Criteria
  • Women taking statins and smokers.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Control GroupControl GroupDid not exercise, during 10 weeks.
High Volume GroupHigh Volume GroupPerformed four weekly sessions, during 10 weeks with 45 to 55 minutes per session.
Low Volume GroupLow Volume GroupPerformed only twice a week, during 10 weeks with 45 to 55 minutes per session.
Primary Outcome Measures
NameTimeMethod
Metabolic outcomes10 weeks

TC/HDL ratio

Secondary Outcome Measures
NameTimeMethod
Secondary outcomes10 weeks

Quality of life

Trial Locations

Locations (1)

Adriana Cristine Koch Buttelli

🇧🇷

Porto Alegre, Rio Grande do Sul, Brazil

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