Health, Fitness, and Safety Knowledge as Determinants of Adverse Events in Recreational Divers in Poland
DIVE-PL
Health Status, Physical Activity, and Safety Knowledge as Determinants of Adverse Events Among Recreational Divers in Poland: a Cross-sectional Online Survey Study
1 other identifier
observational
384
1 country
2
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2026
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 2, 2026
CompletedStudy Start
First participant enrolled
October 1, 2026
CompletedFirst Posted
Study publicly available on registry
October 2, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 31, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
October 31, 2027
October 2, 2026
September 1, 2026
1.1 years
July 2, 2026
October 1, 2026
Conditions
Keywords
Outcome Measures
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.
At enrollment (Day 1; single cross-sectional assessment)
Secondary Outcomes (4)
Estimated VO2max (University of Houston Non-Exercise Test)
At enrollment (Day 1; single cross-sectional assessment)
Diving safety knowledge score
At enrollment (Day 1; single cross-sectional assessment)
Frequency of risky behaviours
At enrollment (Day 1; single cross-sectional assessment)
Adjusted odds ratios for diving-related adverse events
At enrollment (Day 1; single cross-sectional assessment)
Study Arms (1)
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.
Interventions
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.
Eligibility Criteria
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.
You may qualify if:
- 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)
You may not qualify if:
- 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)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
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
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 2, 2026
First Posted
October 2, 2026
Study Start
October 1, 2026
Primary Completion (Estimated)
October 31, 2027
Study Completion (Estimated)
October 31, 2027
Last Updated
October 2, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share