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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02418715
Other study ID # Water-Based Exercise Trial
Secondary ID
Status Completed
Phase N/A
First received April 8, 2015
Last updated April 15, 2015
Start date February 2011
Est. completion date June 2011

Study information

Verified date April 2015
Source Hospital de Clinicas de Porto Alegre
Contact n/a
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Interventional

Clinical Trial Summary

The aim of this study was to investigate the effects of water-based exercises on lipid profile (LP) and lipoprotein lipase (LPL) levels in premenopausal dyslipidemic women.

It was hypothesized that a water-based aerobic interval-training period would decrease plasma concentrations of atherogenic lipoproteins and concomitantly increase HDL and LPL levels, as well as maximal oxygen uptake (VO2max) values.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date June 2011
Est. primary completion date June 2011
Accepts healthy volunteers No
Gender Female
Age group 40 Years to 50 Years
Eligibility Inclusion Criteria:

- Premenopausal

- Sedentary

- Dyslipidemic

- Aged between 40 and 50 years old

Exclusion Criteria:

- Smokers

- Hypolipemic drugs users

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Water Aerobics Training


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Hospital de Clinicas de Porto Alegre

Outcome

Type Measure Description Time frame Safety issue
Other Maximal oxygen uptake (VO2max) values 12 weeks Yes
Primary Lipid Profile Levels (total cholesterol, LDL, HDL, triglycerides) 12 weeks Yes
Secondary Lipoprotein Lipase Levels 12 weeks Yes
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