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Not yet recruitingNCT07855861DIVE-PLUpdated Oct 2, 2026

Health, Fitness, and Safety Knowledge as Determinants of Adverse Events in Recreational Divers in Poland

An observational study in Decompression Sickness, Barotrauma and Recreational Diving, sponsored by Medical University of Bialystok. Not yet recruiting at 2 sites in Poland. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-02.

Sponsored by Medical University of Bialystok · Observational

Updated Oct 2, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
384
Ages
18 Years and older
Sex
All
01

Study summary

This cross-sectional online survey study assesses health status, physical fitness, and safety knowledge as potential determinants of diving-related adverse events among recreational divers in Poland. Recreational diving exposes participants to specific hazards, including decompression sickness (DCS) and barotrauma of the middle ear, sinuses, and lungs. To date, no Polish study has simultaneously evaluated health, physical fitness, theoretical safety knowledge, and the occurrence of adverse events in this population. Adult divers (18 years or older) who completed at least one dive in the past 24 months and reside in Poland complete an anonymous online questionnaire (about 12 to 18 minutes). Physical fitness is estimated as VO2max using the University of Houston Non-Exercise Test (physical activity rating, age, BMI, and sex). Knowledge of DCS, barotrauma, and safe-diving rules is tested at three difficulty levels. The questionnaire also captures diving exposure, certification level, chronic health conditions, and risky behaviours (smoking, alcohol use, and diving beyond certification). The primary endpoint is the proportion of divers reporting at least one diving-related adverse event. Associations with certification level, estimated VO2max, BMI, and other factors are analysed using multivariable logistic regression. The study is non-interventional, anonymous, and carries minimal risk; no clinical procedures or biological sampling are involved.

Read the detailed description

Primary objective: to assess health status, physical fitness, and safety/training knowledge in relation to the occurrence of diving-related adverse events among recreational divers in Poland.

Specific objectives: (1) estimate VO2max from the University of Houston Non-Exercise Test; (2) assess knowledge of decompression sickness, barotrauma, and safe-diving rules at basic, advanced, and emergency-medical levels; (3) determine the frequency of barotrauma and decompression sickness symptoms (clinically confirmed versus presumed); (4) identify risky behaviours (smoking, alcohol use, diving under the influence, and diving beyond certification); (5) assess associations between training level, physical activity, and health and the occurrence of adverse events using multivariable logistic regression.

Hypotheses: H1 - higher certification (Advanced Open Water Diver and above) is associated with better knowledge of diving-related health hazards; H2 - lower estimated VO2max is associated with a higher frequency of adverse events; H3 - risky behaviours are more frequent among lower-certified divers; H4 (exploratory) - decompression sickness risk factors identified in the DAN DSL 2024 dataset are present in the Polish recreational diving population.

Design: cross-sectional, observational, non-interventional study conducted as an anonymous online survey. No clinical procedures, biological sampling, or modification of medical management are involved.

Population and sampling: adults (18 years or older) residing in Poland who completed at least one dive in the past 24 months, recruited online (convenience sampling) via diving organizations, dive centers, and themed social-media communities.

Sample size: target analytic n = 384, derived by triangulation of three methods (proportion estimation n = 323; two-proportion comparison n = 304; logistic-regression events-per-variable rule n = 234), with the binding value (323) plus a 15% non-response buffer.

Data collection and privacy: anonymous online questionnaire hosted on Medical University of Bialystok infrastructure (REDCap); no identifying data and no IP address are stored; processing is GDPR-compliant; data are retained on secured university storage for 5 years and used only for aggregate scientific analysis.

02

Conditions studied

  • Decompression Sickness
  • Barotrauma
  • Recreational Diving

Keywords

  • scuba diving
  • freediving
  • VO2max
  • diving safety
  • adverse events
  • Poland
  • diving safety research
  • physical fitness
03

In context

Decompression Sickness

22 studies on the registry are indexed under Decompression Sickness; 7 are open to participants now.

Browse Decompression Sickness studies →

Lead sponsor

Medical University of Bialystok is the lead sponsor of 68 studies on the registry; 17 are open to participants now.

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

04

Who can participate

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

Study population

Adult recreational divers residing in Poland who completed at least one dive in the past 24 months, recruited online (convenience sampling) via diving organizations (KDP/CMAS-PTTK, PADI, SSI, IANTD, RAID), dive centers, and themed social-media communities.

Inclusion criteria

  • Age 18 years or older
  • At least one dive within the past 24 months
  • Provision of informed consent (checkbox in the survey)
  • Residence in Poland (self-declared)

Exclusion criteria

Exclusion Criteria:

  • Age under 18 years
  • No dive within the past 24 months
  • No consent to participate
  • Incomplete completion of survey sections A-C (eligibility, demographics, diving exposure)
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
384 participants (estimated)
Patient registry
No

Groups and cohorts

  • Recreational divers

    Adults (18 years or older) residing in Poland who completed at least one dive in the past 24 months and complete the anonymous online survey. A single observational cohort assessed cross-sectionally.

    Other: Anonymous online questionnaire

Interventions

  • OtherAnonymous online questionnaire

    Anonymous online questionnaire completed once by each participant (about 12 to 18 minutes). It captures demographic data, diving exposure and certification level, chronic health conditions, risky behaviours, estimated VO2max (University of Houston Non-Exercise Test), and a diving-safety knowledge test. No clinical procedures or biological sampling are involved; this is the observational data-collection instrument for the cohort.

06

What researchers measure

Primary outcomes

  1. Prevalence of diving-related adverse events

    Proportion of divers reporting at least one diving-related adverse event (barotrauma symptoms, decompression sickness symptoms, or other post-dive health problems) occurring at any time during the participant's diving history up to enrollment (lifetime recall). Reported as a percentage with 95% confidence interval.

    Time frame: At enrollment (Day 1; single cross-sectional assessment)

Secondary outcomes

  1. Estimated VO2max (University of Houston Non-Exercise Test)

    Estimated maximal oxygen uptake (mL/kg/min) calculated from the University of Houston Non-Exercise Test (physical activity rating, age, BMI, and sex), summarized as mean with standard deviation and as median with quartiles, stratified by sex and age.

    Time frame: At enrollment (Day 1; single cross-sectional assessment)

  2. Diving safety knowledge score

    Percentage of correct answers on the diving-hazard knowledge test (decompression sickness, barotrauma, and safe-diving rules), reported overall and at three difficulty levels: basic, advanced, and emergency-medical.

    Time frame: At enrollment (Day 1; single cross-sectional assessment)

  3. Frequency of risky behaviours

    Proportion of divers reporting risky behaviours: tobacco use, alcohol use before diving, diving under the influence of alcohol or other substances, and diving beyond their certification level.

    Time frame: At enrollment (Day 1; single cross-sectional assessment)

  4. Adjusted odds ratios for diving-related adverse events

    Adjusted odds ratios (with 95% confidence intervals) for the occurrence of at least one diving-related adverse event, estimated by multivariable logistic regression, for certification level, estimated VO2max, BMI, and selected risk factors from the DAN DSL 2024 dataset (e.g., sex, thermal comfort, pre-dive physical activity).

    Time frame: At enrollment (Day 1; single cross-sectional assessment)

07

Study locations

2 sites
  • Medical University of Bialystok, Department of Respiratory Physiopathology
    Bialystok, Podlaskie Voivodeship 15-540, Poland
  • Medical University of Bialystok, II Department of Lung Diseases, Lung Cancer and Internal Medicine
    Bialystok, Podlaskie Voivodeship 15-540, Poland
    • Robert Mróz, Prof. MD PhD · Contact · lung@umb.edu.pl · +48858316383
    • Jakub Matuk, BEng · Sub investigator
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 2, 2026
Show all 1 update
  1. Oct 2, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07855861
Lead sponsor
Medical University of Bialystok
Responsible party
Sponsor
First posted
Oct 2, 2026
Start date
Oct 1, 2026 (estimated)
Primary completion
Oct 31, 2027 (estimated)
Completion
Oct 31, 2027 (estimated)
Last update
Oct 2, 2026

Study contacts

Lukasz Minarowski, MD, PhD
Contact
lukasz.minarowski@umb.edu.pl
+48 85 831 63 83

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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