- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06371105
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
Intervention / Treatment
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.
Sponsor
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 014_2018
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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