Effects of Water-Based Exercise in Women With Metabolic Syndrome

NCT ID: NCT03210597

Last Updated: 2018-10-12

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

51 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-08-01

Study Completion Date

2018-10-10

Brief Summary

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The objective of the present study was to compare the neuromuscular, cardiorespiratory and metabolic effects of 12 weeks of aerobic training, strength training and combined training in the aquatic environment in women with MS. For this purpose, 51 postmenopausal, sedentary and MS women were randomly divided into three intervention groups: hydro-aerobic (HA, n = 18, 63.77 ± 5.03 years), hydro-power (HF, n = 16, 61.01 ± 4.93 years) and hydro-combined (HC; n = 17; 60.52 ± 6.91). A subsample participated in eight weeks without physical exercise to characterize a control period. The three intervention groups performed two weekly sessions of 60 minutes for 12 weeks. Before and after the training period, blood tests, muscle strength tests, cardiorespiratory evaluation, functional tests and a questionnaire were performed. For statistical analysis, the Generalized Estimates Equations (GEE) model was used, using the "group" and the "time" as factors. The Bonferroni post hoc was used to locate the differences and the significance index adopted was α = 0.05.

Detailed Description

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Water-based exercise as a mode of aquatic exercise has been highlighted in the scientific literature. Research on different models of training, aerobic, muscle strength and combined (aerobic and muscle strength), have already demonstrated their beneficial effects on different physical abilities. Recent studies indicate benefits of water-based exercise for the population with metabolic diseases such as hypertension, type 2 diabetes, dyslipidemias and obesity. However, for subjects with metabolic syndrome (MS) there are few studies that investigated which training model in the aquatic environment could generate physical and metabolic improvements.

This study is characterized as a randomized clinical trial, which treated three intervention groups with physical exercise programs. A subsample participated in a period of eight weeks without physical exercise to characterize a control period. The subjects in this subsample were later randomized into the intervention groups.

Conditions

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Metabolic Syndrome

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors
Participant: During the training period the subjects were not informed about the training modality they were performing and also were not informed about the modalities of the other subjects, only they were informed that hydrogymnastic sessions would be performed.

Outcomes assessor:The team evaluating the outcomes was blinded, not receiving information about the intervention received by the subjects participating in the study

Study Groups

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hydro-aerobic

Water aerobics exercise

Group Type EXPERIMENTAL

Exercise

Intervention Type OTHER

The subjects performed training in aquatic environment

hydro-power

Resistance water exercise

Group Type EXPERIMENTAL

Exercise

Intervention Type OTHER

The subjects performed training in aquatic environment

hydro-combined

Water aerobics and resistance water exercise

Group Type EXPERIMENTAL

Exercise

Intervention Type OTHER

The subjects performed training in aquatic environment

Interventions

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Exercise

The subjects performed training in aquatic environment

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Postmenopausal;
* Sedentary;
* Presented at least three positive components within the five possible to characterize the metabolic syndrome.

Exclusion Criteria

* Smokers.
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

Principal Investigators

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Luiz F. Martins Kruel

Role: STUDY_DIRECTOR

Federal Universty of Rio Grande do Sul

Other Identifiers

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CEP UFRGS 1.499.603

Identifier Type: -

Identifier Source: org_study_id

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