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Cognitive Responses to Acute Breath-Hold Diving Training in Female Divers

Investigation of Cognitive Responses to Acute Breath-Hold Diving Training in Female Divers

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07616804
Enrollment
30
Registered
2026-06-01
Start date
2026-06-01
Completion date
2026-09-15
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Performance, Sport Physiology

Brief summary

This study aims to investigate the acute cognitive and physiological responses to breath-hold diving training in trained female divers. Participants will complete three separate sessions including a control session, a land-based breath-hold training session, and a water-based breath-hold training session in randomized order. Cognitive performance, mood state, heart rate responses, respiratory function, and maximal breath-hold capacity will be evaluated before and after the interventions. The study is expected to improve understanding of how acute apnea-based diving exercises influence cognitive functions and physiological adaptations under different environmental conditions.

Interventions

BEHAVIORALLand-Based Breath-Hold Training

Participants will perform structured land-based breath-hold exercises consisting of repeated apnea efforts at 60% of individual maximal breath-hold capacity with standardized rest intervals.

BEHAVIORALWater-Based Breath-Hold Training

Participants will perform structured breath-hold exercises in a swimming pool environment consisting of repeated apnea efforts at 60% of individual maximal breath-hold capacity with standardized rest intervals.

Participants will undergo baseline cognitive, respiratory, mood, and physiological assessments without structured apnea or breath-hold exercise intervention.

Sponsors

Istanbul Gelisim University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Masking description

No masking procedures will be applied because participants and investigators will be aware of the intervention conditions during the sessions.

Intervention model description

Participants will complete control, land-based breath-hold, and water-based breath-hold sessions in randomized crossover order. Cognitive, physiological, and mood-related responses will be evaluated before and after each session.

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Licensed breath-hold or free-diving athletes * Aged between 18 and 30 years * Minimum of 5 years of training experience * No known cardiovascular or pulmonary disease * Non-smokers * Willing to participate voluntarily * Refraining from intense exercise within 24 hours before testing

Exclusion criteria

* Use of performance-enhancing drugs or ergogenic aids * Presence of chronic sports injury * Alcohol consumption within 24 hours before testing * Caffeine intake within 2 hours before testing * Sleep deprivation or severe fatigue * Current medication use Fear of water or inability to complete breath-hold procedures

Design outcomes

Primary

MeasureTime frameDescription
Working Memory Accuracy (2-Back Test)Baseline and immediately after the intervention, within 5 minutes post-intervention.Accuracy score obtained from the computerized 2-back cognitive task.
Reaction Time During the 2-Back TestBaseline and immediately after the intervention, within 5 minutes post-intervention.Mean reaction time recorded during correct responses in the 2-back cognitive task.

Secondary

MeasureTime frameDescription
Brunel Mood Scale (BRUMS) Total ScoreBaseline and immediately after the intervention, within 5 minutes post-intervention.Total mood disturbance score assessed using the Brunel Mood Scale questionnaire.
Maximum Breath-Hold DurationBaseline during the control session before intervention sessions.Maximum voluntary breath-hold duration recorded during testing.
Resting Heart RateBefore each experimental session.Resting heart rate measured before each session using a Polar heart rate monitor.
Exercise Heart Rate ResponseDuring the intervention session.Heart rate responses recorded every 30 seconds during the breath-hold exercise protocol.

Countries

Turkey (Türkiye)

Contacts

CONTACTGörkem Açar, Ress. Asst.
gacar@gelisim.edu.tr+90 545 407 01 98

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 2, 2026