- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03519620
Swimming and Water Walking on Spirometry Values (ESWWSV)
May 8, 2018 updated by: Samuel Honório, Instituto Politécnico de Castelo Branco
The Effects of Swimming and Swimming Complemented With Water Walking on Spirometry Values
To study the effects of swimming with water walking in children aged between 6 and 12 years in terms of spirometric values.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The present research aims to verify if there are differences in body composition and spirometric values in children aged between 6 and 12 years who practice swimming complemented with water walking at the end of each session and those who only practice swimming.
The sample consisted of 28 individuals aged 6 to 12 years and was divided into two groups: swimming group (SG) with 9 children and swimming complemented with water walking group (SWWG) of 19 children.
In this study, the investigators wanted to know which were the benefits in body composition and for that purpose used a bio-impedance scale Targa Silvercrest Z29777A (Germany), and an anthropometric tape to measure the waist circumference.
To calculate the spirometric values, namely forced vital capacity (FVC), forced expiratory volume in 1 second (FEV1) and even peak expiratory flow (PEF) a Cosmed Microquark spirometer was used.
In terms of statistical procedures, the investigators used the program Statistical Package for the Social Sciences version number 20 (SPSS 20.0).
The investigators used descriptive statistics (minimum, maximum, means and standard deviations), the Shapiro Wilk test for testing the normality of the sample, inferential statistics (non-parametric Mann-Whitney tests, Friedman's Anova, and for the calculation of the effect magnitude the d-Cohen test).
After the data treatment, regarding the inter-group analysis (comparison between the swimming group and the swimming group with water walking) the investigators observed that there were significant differences in three variables at the end of the study, that is, at the end of the 3 moments.
These variables were weight relative to body composition, forced expiratory volume in 1 second (FEV1) and peak expiratory flow (PEF), these values are relative to the spirometry evaluation.
Concerning intra-group differences (improvement in the swimming group and the swimming with water walking group in the three moments evaluated), the SWWG showed significant improvements in the variables of weight, muscle mass, fat mass, percentage of water, body mass index (BMI), body percentiles, forced vital capacity (FVC) and forced expiratory volume in 1 second (FEV1).
Study Type
Interventional
Enrollment (Actual)
28
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
-
-
-
Castelo BRanco, Portugal, 6000
- Municipal Swimming Pools
-
-
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
6 years to 12 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Children inside this age range;
- water experience between 6 and 12 months
- children with no other activities besides swimming
Exclusion Criteria:
- Children with Asma;
- Children with DPOC
- Children with pulmonary limitations.
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: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: SWWSV
Spirometric Values: Forced Vital Capacity; Forced Expiratory Volume in 1 second; Peak Expiratory Flow
|
Behaviours to prevent child obesity
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Forced Vital Capacity
Time Frame: 12 weeks
|
described in liters
|
12 weeks
|
|
Forced Expiratory Volume in 1 second
Time Frame: 12 weeks
|
described in liters
|
12 weeks
|
|
Peak Expiratory Flow
Time Frame: 12 weeks
|
described in liters
|
12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Fat mass
Time Frame: 12 weeks
|
described in percentage
|
12 weeks
|
|
Weight
Time Frame: 12 weeks
|
described in kilograms
|
12 weeks
|
|
Height
Time Frame: 12 weeks
|
described in meters
|
12 weeks
|
|
weight and height will be combined to report BMI
Time Frame: 12 weeks
|
BMI described in kg/m^2
|
12 weeks
|
|
Muscle mass
Time Frame: 12 weeks
|
described in percentage
|
12 weeks
|
|
waist circumference
Time Frame: 12 weeks
|
described in centimeters
|
12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: João B Oliveira, Master, Castelo Branco
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)
March 3, 2018
Primary Completion (Actual)
March 3, 2018
Study Completion (Actual)
March 3, 2018
Study Registration Dates
First Submitted
April 16, 2018
First Submitted That Met QC Criteria
May 8, 2018
First Posted (Actual)
May 9, 2018
Study Record Updates
Last Update Posted (Actual)
May 9, 2018
Last Update Submitted That Met QC Criteria
May 8, 2018
Last Verified
May 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IPCB
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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