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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03210597
Other study ID # CEP UFRGS 1.499.603
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 1, 2016
Est. completion date October 10, 2018

Study information

Verified date October 2018
Source Federal University of Rio Grande do Sul
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 51
Est. completion date October 10, 2018
Est. primary completion date December 28, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Postmenopausal;

- Sedentary;

- Presented at least three positive components within the five possible to characterize the metabolic syndrome.

Exclusion Criteria:

- Smokers.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exercise
The subjects performed training in aquatic environment

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Federal University of Rio Grande do Sul

Outcome

Type Measure Description Time frame Safety issue
Primary Systolic and diastolic blood pressure mmHg 12 weeks
Secondary Strength tests: Maximum dynamic muscle strength One repetition test: how many kilograms the subject is able to withstand on a repetition of elbow flexion and knee extension exercise 12 weeks
Secondary EMG test Maximum isometric amplitude of the electromyographic signal of the vastus lateralis and rectus femoris muscles 12 weeks
Secondary Time Up and go test How long (in seconds) the subject needs to lift from a chair, walk 2.44 meters, and sit in a chair again 12 weeks
Secondary Sit and Stand test How often in 30 seconds the subject is able to get up and sit on a chair. 12 weeks
Secondary Triglyceride levels blood test: mg/dl 12 weeks
Secondary HDL cholesterol levels blood test: mg/dl 12 weeks
Secondary Fasting blood glucose levels blood test: mg/dl 12 weeks
Secondary Waist circumference centimeters 12 weeks
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