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AsthmaSWANNCT03017976

Swimming Pool Environment Impact on the Human Respiratory Health

An observational study of Asthma and Lung Disease, run by Universidade do Porto at 1 site in Portugal.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial 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 more about this study

Who is it for?
Ages 12 years and olderHealthy volunteers can take part
Conditions the study is for
Asthma, Lung Disease, Genotoxicity
How many people
1,000 participants
Where
1 sitePortugal
Study dates
Jan 2017to Jul 2018
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 12 years and older
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

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

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.

Trial locations and contacts

1 site in 1 country.

Portugal1 site
  • Faculty of Medicine of Porto University

    Porto, Porto District, 4200-319

    André Moreira, MD, PhD, 00351932730090, andremoreira@med.up.pt

    Vânia Mendes, MSc, 00351918567504, vaniamendes@med.up.pt

Other trials in Portugal

About this study

Official title: Swan Study: Swimming Pool Environment Impact on the Human Respiratory Health

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:
  3. 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.
  4. 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:
  3. 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.
  4. 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.

Medical subject headings
Asthma, Lung Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT03017976
Study groupRoleWhat they receive
Competitive swimmersRegular 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 staffSwimming 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.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Spirometry with bronchodilation

    Measured: First week after recruitment

  2. Airway resistance measurement

    Measured: First week after recruitment

  3. Airway reactance measurement

    Measured: First week after recruitment

  4. Fractional concentration of orally exhaled nitric oxide

    Measured: First week after recruitment

  5. Volatile organic compounds in the exhaled breath condensate

    Measured: First week after recruitment

Secondary outcomes (3)
  1. Diagnosis of immunoglobulin E (IgE) mediated allergies by skin prick testing

    Measured: First week after recruitment

  2. Autonomic nervous system function assessment by pupillometry

    Measured: First week after recruitment

  3. Transepidermal water loss

    Measured: First week after recruitment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Jan 2017 (estimated)
  2. Study startJan 2017
  3. Primary completionMar 2017 (estimated)
  4. Study completionJul 2018 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case crossover
Time perspective
Cross-sectional
Enrolment
1,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03017976
Sponsor's protocol ID
NORTE-01-0145-FEDER-000010
Acronym
SWAN
Status last verified
Oct 2016
First submitted
22 Dec 2016
Last updated
11 Jan 2017
Results posted
No
Data monitoring committee
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Asthma and Lung Disease, run by Universidade do Porto at 1 site in Portugal.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 11 Jan 2017. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Portugal. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Spirometry with bronchodilation (time frame: First week after recruitment). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Jan 2017.

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