CClinicalTrials.gg
Status unknownNCT03017976SWANUpdated Jan 11, 2017

Swimming Pool Environment Impact on the Human Respiratory Health

An observational study in Asthma, Lung Disease and Genotoxicity, sponsored by Universidade do Porto. Status unknown at 1 site in Portugal. Open to participants aged 12 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-01-11.

Sponsored by Universidade do Porto · Observational

The sponsor has not verified this record recently (last verified Oct 2016), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Case-crossover
Time perspective
Cross-sectional
Enrollment
1,000
Ages
12 Years and older
Sex
All
01

Study summary

This study aims to assess the influence of exposure to swimming pool environment on respiratory symptoms and diseases, and on cancer outcomes among swimmers and swimming pool attendants.

Read the detailed description

Objectives:

  1. In relation to human exposure 1.1. To assess the levels of certain disinfection by-products (DBPs) in blood and urine (biomarkers of exposure); 1.2. To assess swimming induced changes in biomarkers of genotoxicity, specifically micronuclei (MN) in exfoliated urothelial cells and buccal cells and DNA damage in peripheral blood lymphocytes, urine mutagenicity and in exfoliated urothelial; 1.3. To assess the effects of swimming pool exposure on oxidative stress and lung damage in swimming pool users; 1.4. To assess the impact of DBPs, including volatile DBPs on airway function, inflammation and reactivity; 1.5. To assess the impact of swimming on skin transepidermal water loss and dermal condition.
  2. In relation to swimming pool environment 2.1. To assess water and air quality through the analysis of several chemical (DBPs and other), physicochemical and microbiological parameters and the associated short-term variation of their levels (hourly and daily); 2.2. To assess microbiological contamination of highly used surfaces; 2.3. To assess mutagenicity of indoor chlorinated and brominated swimming pool water.

Methods

Study setting Chlorinated and brominated public indoor municipal swimming pools in the North of Portugal.

Study design

This study will follow two distinct approaches:

  1. A cross-sectional analysis to assess swimming pool physicochemical and microbiological characteristics and the association between each parameter measured as an indicator of water and air quality, contamination of surfaces and the health parameters assessed in recreational users, swimming teachers and pool attendants.
  2. An uncontrolled, before and after study to assess acute and chronic environmental exposure effects on respiratory biomarkers of competitive swimmers:

    1. Assessment of acute changes: regular competitive swimmers will be asked to swim for 40 minutes in a single, indoor, 50 m-long chlorinated swimming pool. Before and after swimming, a battery of measurements will be assessed to evaluate respiratory health biomarkers.
    2. Assessment of chronic changes: regular and naïf competitive swimmers will be followed for a mean period of 90 days. A battery of measurements and biological samples will be collected at the baseline evaluation and 90 days after, in order to evaluate long-term changes in respiratory health biomarkers.

Recruitment and data collection procedures

  1. Cross-sectional study. The cross-sectional analysis will be performed in fifty municipal indoor swimming pools in the North of Portugal on a voluntary basis. The administrative boards of each swimming pool will be approached by the research team to present the study's purposes and procedures and to obtain their consent to perform the study. Upon acceptance, recreational users, swimming coaches/teachers and pool attendants will be contacted and invited to participate. All subjects will receive a written description of the study (appendix I-a) and the informed consent form (appendix II-a). Those who provide an informed consent signed by both the subject and legal tutor (if a minor) will be included in the study. Recreational swimmers, swimming teachers and pool attendants will be asked to complete a self-administered standardized home questionnaire comprising sociodemographic and health-related information, with a major focus on respiratory health. Participants will also be asked to provide information on their food consumption, physical activity levels and psychological well-being. Subjects should return the completed questionnaires at the swimming pool facilities. A medical examination will also be performed by trained health professionals and will include anthropometric measurements, blood pressure evaluation, urine sample collection, skin prick testing, exhaled breath condensate collection, lung function evaluation by spirometry with bronchodilation, in a period conveniently scheduled with the participating subjects.

    The assessment of swimming pool chemical (DBPs and others), physicochemical and microbiological characteristics will include sampling in the water, air and eventually selected surfaces, that include: pool edges, stairs and starting blocks, floors (pool and bathhouse), walls (concrete and glass of the pool and bathhouse) and highly touched surfaces such as bathhouse benches. We will measure different chemical, physicochemical and microbiological parameters in multiple locations within the pool structure in order to characterize the exposure and its spatial and temporal distribution both within a specific swimming pool and also between the different swimming pools studied.

  2. Uncontrolled, before and after study. A single, indoor, 50-meter-long chlorinated swimming pool in Porto, Portugal, will be selected for this study. The administrative board will be approached by the research team to present the study's purposes and procedures and to obtain their consent to perform the study. Upon acceptance, the competitive swimming team will be asked to participate in the study. All subjects will receive a written description of the study (appendix I-b) and the informed consent form (appendix II-b). Competitive swimmers with 12 years of age or older who provide an informed consent signed by both the subject and legal tutor (if a minor) will be included in an uncontrolled before and after study to assess acute and chronic respiratory symptoms after a regular training session. This assessment will be executed following two approaches:

    1. Assessment of acute changes: in a period conveniently scheduled with the swimmers and their coaches, a medical examination will be performed in order to assess baseline respiratory biomarkers of competitive swimmers. This examination will include the assessment of exhaled breath condensate and lung function evaluation. The same biological measurements will be performed after a single regular training session and an interviewer-administered questionnaire will be applied.
    2. Assessment of chronic changes: Competitive swimmers will also be followed through a 90-day period in order to evaluate long-term changes in respiratory and cancer biomarkers. The baseline evaluation will consist in the assessment of biological measurements, namely anthropometric measurements, blood pressure evaluation, sample collection (i.e. blood and urine samples and buccal swab), skin prick testing, pupillometry, capsaicin challenge, exhaled breath condensate collection, lung function evaluation (namely, spirometry with bronchodilation, impulse oscillometry, methacholine challenge and fractional concentration of orally exhaled nitric oxide) and transepidermal water loss assessment. Participants will also be asked to provide information on sociodemographic characteristics, personal and family history of disease, use of medication, frequency of self-reported respiratory, ocular and cutaneous symptoms, data on health-related behaviors, namely tobacco use, physical activity levels and food consumption, through an interviewer-administered questionnaire. A full examination will be performed only at baseline and at the follow-up assessment (90 days after).

This evaluation will be performed by trained health professionals in a room inside the swimming pool facilities but separated from the swimming pool area, in a period conveniently scheduled with the swimmers and their coaches. Due to the possibility of experiencing transient symptoms, participants will be asked to visit the research department in order to perform the methacholine challenge. Participants will be reimbursed for any travel expenses.

02

Conditions studied

  • Asthma
  • Lung Disease
  • Genotoxicity

Browse trials for

03

In context

Lung Diseases

3,303 studies on the registry are indexed under Lung Diseases; 355 are open to participants now.

This study's planned enrollment of 1,000 is above the median of 157 across 929 observational studies indexed under Lung Diseases.

Browse Lung Diseases studies →

Lead sponsor

Universidade do Porto is the lead sponsor of 170 studies on the registry; 52 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
12 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Competitive swimmers, recreational users and swimming pool workers attending chlorinated and brominated public indoor municipal swimming pools in the North of Portugal.

Eligibility criteria

Competitive swimmers, recreational swimmers or pool workers of a participating indoor swimming pool; Individuals with 12 years of age or older; Individuals who provide (or their caregivers) a signed informed consent.

05

Study design

Observational model
Case-crossover
Time perspective
Cross-sectional
Enrollment
1,000 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Competitive swimmers

    Regular and naïf competitive swimmers will be followed for a mean period of 90 days. A battery of measurements and biological samples will be collected at the baseline evaluation and 90 days after, in order to evaluate long-term changes in respiratory health biomarkers. Measurements will also be performed before and after a single regular training session in order to assess acute effects in respiratory health biomarkers.

  • Recreational swimmers and swimming pool staff

    Swimming pool physicochemical and microbiological characteristics and the association between each parameter measured as an indicator of water and air quality, contamination of surfaces will be evaluated and the association with recreational users, swimming teachers and pool attendants health parameters will be studied.

06

What researchers measure

Primary outcomes

  1. Spirometry with bronchodilation

    Time frame: First week after recruitment

  2. Airway resistance measurement

    Time frame: First week after recruitment

  3. Airway reactance measurement

    Time frame: First week after recruitment

  4. Fractional concentration of orally exhaled nitric oxide

    Time frame: First week after recruitment

  5. Volatile organic compounds in the exhaled breath condensate

    Time frame: First week after recruitment

Secondary outcomes

  1. Diagnosis of immunoglobulin E (IgE) mediated allergies by skin prick testing

    Time frame: First week after recruitment

  2. Autonomic nervous system function assessment by pupillometry

    Time frame: First week after recruitment

  3. Transepidermal water loss

    Time frame: First week after recruitment

07

Study locations

1 site
  • Faculty of Medicine of Porto University
    Porto, 4200-319, Portugal
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 11, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03017976
Lead sponsor
Universidade do Porto
Responsible party
Sponsor
First posted
Jan 11, 2017
Start date
Jan 2017
Primary completion
Mar 2017 (estimated)
Completion
Jul 2018 (estimated)
Last update
Jan 11, 2017

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2016. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion