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

NCT ID: NCT03307031

Last Updated: 2017-10-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

26 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-03-01

Study Completion Date

2017-09-13

Brief Summary

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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

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Conditions

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Dyslipidemias

Keywords

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training volume elderly lipid profile postmenopausal

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

A CONTROLLED CLINICAL TRIAL
Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Investigators Outcome Assessors

Study Groups

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High Volume Group

Performed four weekly sessions, during 10 weeks with 45 to 55 minutes per session.

Group Type EXPERIMENTAL

High Volume Group

Intervention Type OTHER

Performed four weekly session, during 10 weeks with 45 to 55 minutes per session.

Low Volume Group

Performed only twice a week, during 10 weeks with 45 to 55 minutes per session.

Group Type EXPERIMENTAL

Low Volume Group

Intervention Type OTHER

Performed only twice a week, during 10 weeks with 45 to 55 minutes per session.

Control Group

Did not exercise, during 10 weeks.

Group Type PLACEBO_COMPARATOR

Control Group

Intervention Type OTHER

Did not exercise, during 10 weeks.

Interventions

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High Volume Group

Performed four weekly session, during 10 weeks with 45 to 55 minutes per session.

Intervention Type OTHER

Low Volume Group

Performed only twice a week, during 10 weeks with 45 to 55 minutes per session.

Intervention Type OTHER

Control Group

Did not exercise, during 10 weeks.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Dyslipidemic, postmenopausal and sedentary.

Exclusion Criteria

* Women taking statins and smokers.
Minimum Eligible Age

60 Years

Maximum Eligible Age

75 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Federal University of Rio Grande do Sul

OTHER

Sponsor Role lead

Responsible Party

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Luiz Fernando Martins Kruel

Doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Adriana Cristine Koch Buttelli

Porto Alegre, Rio Grande do Sul, Brazil

Site Status

Countries

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Brazil

Other Identifiers

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1.990.955

Identifier Type: -

Identifier Source: org_study_id