Aquatic_Training in Obese Women

April 14, 2024 updated by: YUNG-SHENG CHEN, University of Taipei

Effect of Water-based Aerobic Training on Anthropometric, Biochemical, Cardiovascular, and Explosive Strength Parameters in Young Overweight and Obese Women

This study aims to assess the effects of 10-week water-based aerobic training (thrice a week) on anthropometrics, biochemicals, cardiovascular parameters, and explosive strength in young overweight and obese women. The findings indicate that water-based aerobic training could be a useful program to enhance body composition, biochemical, cardiovascular, and explosive strength parameters in young overweight and obese women compared to inactive persons

Study Overview

Status

Completed

Conditions

Detailed Description

This study is based on a randomized controlled trial with a pre-to-post testing design, twenty-seven young overweight and obese women were assigned to training group (a water-based aerobic training) or control group (maintaining their usual activities during the studying period. For each training session, water activities were implemented for 50 min which included warm-up (10 min), main activities (30 min), and cool-down (10 min). The swimming pool where the intervention took part was 1.50 m deep of water. The pre- and post-intervention participants were assessed for their anthropometrics, biochemicals (fasting glycemia, total cholesterol, high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol and triglyceride (TG)), resting blood pressure, and resting heart rate, and explosive strength of upper (countermovement jump and squat jump) and lower limbs (a seated medicine ball throw test).

Study Type

Interventional

Enrollment (Actual)

31

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Taipei, Taiwan, 11153
        • Department of Exercise and Health Sciences, University of Taipei

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Age between 20 and 35 years
  • Sedentary lifestyle within six month
  • Not using drugs or other therapy for obesity.

Exclusion Criteria:

  • BMI below 25.0 and over 34.9 kg.m-2
  • having any infectious or skin diseases

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Training group
Performing a 10-week water-based aerobic training (thrice/week)
The water-based aerobic program was adopted from the protocol previously used by Costa et al. (2018, 2020). This training program was carried out thrice a week over 2 non-consecutive days 48 hours apart for 10 weeks according to ACSM guidelines
No Intervention: Control group
Maintaining their usual activities during the interventional period

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
fasting glycemia in millimoles per liter
Time Frame: 3 days before the 10-week interventional period
baseline blood sample
3 days before the 10-week interventional period
total cholesterol in millimoles per liter
Time Frame: 3 days before the 10-week interventional period
baseline blood sample
3 days before the 10-week interventional period
high-density lipoprotein cholesterol in millimoles per liter
Time Frame: 3 days before the 10-week interventional period
baseline blood samplelipoprotein cholesterol, and triglyceride concentrations
3 days before the 10-week interventional period
low-density lipoprotein cholesterol in millimoles per liter
Time Frame: 3 days before the 10-week interventional period
baseline blood sample
3 days before the 10-week interventional period
triglyceride concentrations in millimoles per liter
Time Frame: 3 days before the 10-week interventional period
baseline blood sample
3 days before the 10-week interventional period
systolic blood pressure in millimeters of mercury
Time Frame: 3 days before the 10-week interventional period
baseline blood sample
3 days before the 10-week interventional period
diastolic blood pressure in millimeters of mercury
Time Frame: 3 days before the 10-week interventional period
baseline blood sample
3 days before the 10-week interventional period
heart rate in beat per minute
Time Frame: 3 days before the 10-week interventional period
baseline blood sample
3 days before the 10-week interventional period
fasting glycemia in millimoles per liter
Time Frame: one day after the 10-week interventional period
post-training blood sample
one day after the 10-week interventional period
total cholesterol in millimoles per liter
Time Frame: one day after the 10-week interventional period
post-training blood sample
one day after the 10-week interventional period
high-density lipoprotein cholesterol in millimoles per liter
Time Frame: one day after the 10-week interventional period
post-training blood sample
one day after the 10-week interventional period
low-density lipoprotein cholesterol in millimoles per liter
Time Frame: one day after the 10-week interventional period
post-training blood sample
one day after the 10-week interventional period
triglyceride concentrations in millimoles per liter
Time Frame: one day after the 10-week interventional period
post-training blood sample
one day after the 10-week interventional period
systolic blood pressure in millimeters of mercury
Time Frame: one day after the 10-week interventional period
post-training blood sample
one day after the 10-week interventional period
diastolic blood pressure in millimeters of mercury
Time Frame: one day after the 10-week interventional period
post-training blood sample
one day after the 10-week interventional period
heart rate in beat per minute
Time Frame: one day after the 10-week interventional period
post-training blood sample
one day after the 10-week interventional period

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
countermovement jump in centimetres
Time Frame: 3 days before the 10-week interventional period
baseline lower limbs power test
3 days before the 10-week interventional period
squat jump in centimeters
Time Frame: 3 days before the 10-week interventional period
baseline lower limbs power test
3 days before the 10-week interventional period
chest 3-kg medicine ball throw in meters
Time Frame: 3 days before the 10-week interventional period
baseline upper limbs power test
3 days before the 10-week interventional period
countermovement jump in centimetres
Time Frame: one day after the 10-week interventional period
post-training lower limbs power test
one day after the 10-week interventional period
squat jump in centimeters
Time Frame: one day after the 10-week interventional period
post-training lower limbs power test
one day after the 10-week interventional period
chest 3-kg medicine ball throw in meters
Time Frame: one day after the 10-week interventional period
post-training upper limbs power test
one day after the 10-week interventional period

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Yung-Sheng Chen, Ph.D., Department of Exercise and Health Sciences, University of Taipei

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 2, 2019

Primary Completion (Actual)

March 30, 2019

Study Completion (Actual)

March 30, 2019

Study Registration Dates

First Submitted

March 28, 2024

First Submitted That Met QC Criteria

April 14, 2024

First Posted (Actual)

April 17, 2024

Study Record Updates

Last Update Posted (Actual)

April 17, 2024

Last Update Submitted That Met QC Criteria

April 14, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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