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Beta Caryophyllene & Apnea Performance

Effects of Beta Caryophyllene Supplementation on Autonomic Regulation and Apnea Performance in Elite Divers - a Randomized Crossover Trial

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07340996
Enrollment
15
Registered
2026-01-14
Start date
2026-01-01
Completion date
2026-12-31
Last updated
2026-01-14

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

Conditions

EXERCISE PERFORMANCE

Keywords

freediving

Brief summary

The purpose of this study is to investigate whether β-caryophyllene supplementation can enhance the static apnea capacity of freedivers.

Detailed description

Using a randomized crossover design with double-blind methodology, participants were assigned to either the β-caryophyllene trial (BCP) trial or the placebo (PLA) trial, which without β-caryophyllene. Participants consumed either 200 mg of β-caryophyllene capsules (BCP trial) or placebo capsules (PLA trial) based on pre-test results. After a 30-minute rest period and warm-up, a single maximal voluntary static breath-hold test was conducted. Breath-hold duration and physiological and salivary biochemical indicators before and after the breath-hold test were observed.

Interventions

DIETARY_SUPPLEMENTinterventions

supplementation of β-caryophyllene

DIETARY_SUPPLEMENTPlacebo

Participants consumed placebo capsules (PLA trial)

Sponsors

National Science and Technology Council, Taiwan
CollaboratorOTHER_GOV
Chih-Hui Chiu
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Masking description

placebo

Intervention model description

randomized crossover design with double-blind methodology

Eligibility

Sex/Gender
MALE
Age
20 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* With over 3 years of freediving experience

Exclusion criteria

* Without over 3 years of freediving experience

Design outcomes

Primary

MeasureTime frameDescription
Breath-hold duration30 minutes after interventionMeasure the duration of static breath-holding

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026