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Investigating the effectiveness of Elderberry capsules in the prevention of upper respiratory symptoms associated with long distance travel.

Randomised, double-blind, placebo-controlled trial of Elderberry supplementation preventing upper respiratory symptoms in air travellers.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612001301853
Enrollment
280
Registered
2012-12-17
Start date
2013-04-26
Completion date
2014-12-10
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

This study will investigate the effectiveness of Elderberry lozenges in the prevention of upper respiratory symptoms associated with long distance travel.

Interventions

Elderberry capsules (active) are 300mg of standardised Elderberry membrane filtered extract powder (22% polyphenols, 15% anthocyanins) and 150mg of rice flour. Participants will take 2 capsules per 24 hour period for 10 days prior to travel, 3 capsules per 24 hour during travel and a further 4 days at their destination. Trial participation lasts 16 days including the first 4 or 5 days on arriving at their destinations. Travel duration will differ between participants and should not exceed 72 hou

Elderberry capsules (active) are 300mg of standardised Elderberry membrane filtered extract powder (22% polyphenols, 15% anthocyanins) and 150mg of rice flour. Participants will take 2 capsules per 24 hour period for 10 days prior to travel, 3 capsules per 24 hour during travel and a further 4 days at their destination. Trial participation lasts 16 days including the first 4 or 5 days on arriving at their destinations. Travel duration will differ between participants and should not exceed 72 hours of travel. Travel duration is defined as leaving home to arriving at the accommodation at the destination.

Sponsors

Griffith University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Blinded (masking used) (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1) travelling a minimum of 7 hours flight 2) travelling via economy class 3) planning a minimum stay of 4 days at destination

Exclusion criteria

1) Diagnosed respiratory disease 2) Lactation or pregnancy 3) Pollen/plant allergy 4) Serious inflammatory or immunological conditions

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026