ClinicalTrials.gg
Status unknownNCT06479993Updated Jun 28, 2024

The Influence of Chlorella Supplementation on Running Performance

An interventional study of Chlorella supplementation and Placebo supplementation in Athletes and Healthy, sponsored by University College, London. Status unknown at 1 site in United Kingdom. Open to participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-06-28.

Sponsored by University College, London · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Feb 2024), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study summary

Algae, such as chlorella, are gaining popularity as a nutritious additive to whole food or as a supplement. They contain a variety of beneficial nutrients like vitamins, minerals, healthy fats, and amino acids, which can have positive effects on our health and possibly athletic performance. Chlorella, specifically, is a type of single-celled green algae that you can easily find in health stores worldwide. While there's some evidence suggesting that chlorella supplementation might improve submaximal and maximal performance for cyclists, it's unclear if it has the same impact on runners. To investigate this, the investigators aim to conduct a double-blind randomised placebo controlled study to see if taking chlorella daily for 3-weeks can enhance different aspects of running performance, both during low/moderate and intense exercise, among individuals who regularly engage in running.

Read the detailed description

After signing the consent form, we will invite you to come to the ISEH laboratory on Tottenham Court Road so we can take some basic baseline readings. This should last up to 60 minutes and will also include a V̇o2max Test (visit 1). After this, you will be randomly allocated either start on chlorella or placebo first. After supplementation (for visit 2 and 3) you will be required to perform a submaximal running test which will entail running at 60% GET (gas exchange threshold), 80% GET, and 75% of the change from peak. This will then be shortly followed by an incremental test to fatigue.

You will then be required to undergo the exact same supplementation period on the alternative supplement with the same exercise test performed.

You will be required to come into the laboratory a total of 3 times. Each visit should take roughly 1 - 1.5 hours.

02

Conditions studied

  • Athletes
  • Healthy

Keywords

  • Running
  • VO2max
  • Lactate
  • Oxygen Consumption
03

In context

Lead sponsor

University College, London is the lead sponsor of 648 studies on the registry; 146 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 2 (33%) have results posted.

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

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Aged 18-50.
  • Run regularly (3-4 times a week).
  • Train with a purpose to compete.
  • Consider running to be your main sport.
  • Be comfortable running continuously for over 30-minutes at moderate intensity.
  • Represent a local running club.

Exclusion criteria

Exclusion Criteria:

  • Individuals taking blood thinners.
  • Known allergies to algae/mould and iodine.
  • Any illness/conditions identified on PARQ (please see attached PARQ)
  • Taking immunosuppressant medication
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Double (Participant, Investigator)
Enrollment
20 participants (estimated)

Study arms

  • Experimental
    Chlorella supplementation

    Supplementation of chlorella (6g/day for 3-weeks)

    Dietary Supplement: Chlorella supplementation

  • Placebo comparator
    Placebo supplementation

    Supplementation of placebo (6g/day for 3-weeks)

    Dietary Supplement: Placebo supplementation

Interventions

  • Dietary supplementChlorella supplementation

    Supplementation with chlorella (6g/day for 3-weeks)

  • Dietary supplementPlacebo supplementation

    Supplementation with placebo - microcrystalline cellulose (6g/day for 3-weeks)

06

What researchers measure

Primary outcomes

  1. Changes in maximal oxygen uptake

    Changes in cardiovascular fitness variables as measured by a Cardio Pulmonary Exercise Test following the submaximal run.

    Time frame: Following each 3-week supplementation period of either chlorella or placebo

  2. Changes in oxygen consumption and oxygen cost

    Assessing the possible changes in oxygen consumption and oxygen cost (ml/kg/min) at 60% Gas Exchange threshold (GET), 80% GET, and 75% change as measured by a metabolic cart (Vyntus)

    Time frame: Following each 3-week supplementation period of either chlorella or placebo

  3. Changes in the respiratory exchange ratio

    Assessing the possible changes in the respiratory exchange ratio at 60% Gas Exchange threshold (GET), 80% GET, and 75% change as measured by a metabolic cart (Vyntus)

    Time frame: Following each 3-week supplementation period of either chlorella or placebo

  4. Changes in heart rate

    Assessing the possible changes in heart rate (bpm) at 60% Gas Exchange threshold (GET), 80% GET, and 75% change as measured by a metabolic cart (Vyntus)

    Time frame: Following each 3-week supplementation period of either chlorella or placebo

  5. Changes in lactate

    Assessing the possible changes in blood lactate at 60% Gas Exchange threshold (GET), 80% GET, and 75% change, at maximal oxygen uptake, and 15-mins post maximal as measured by the Biosen.

    Time frame: Following each 3-week supplementation period of either chlorella or placebo

  6. Changes in glucose

    Assessing the possible changes in blood glucose at 60% Gas Exchange threshold (GET), 80% GET, and 75% change, at maximal oxygen uptake, and 15-mins post maximal as measured by the Biosen.

    Time frame: Following each 3-week supplementation period of either chlorella or placebo

Secondary outcomes

  1. Changes in nutritional status

    Assessing the possible changes in nutritional status (macro and micronutrient intake) as measured by food recall.

    Time frame: Following each 3-week supplementation period of either chlorella or placebo

07

Study locations

1 of 1 sites recruiting
  • University Colllege London (ISEH)
    London, W1T 7HA, United Kingdom
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 28, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06479993
Responsible party
Sponsor
First posted
Jun 28, 2024
Start date
Jan 5, 2024
Primary completion
May 2025 (estimated)
Completion
Sep 2025 (estimated)
Last update
Jun 28, 2024

Study contacts

Tom Gurney
Contact
t.gurney@ucl.ac.uk
020 3447 2800
Tom Gurney
principal investigator · University College, London

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 status unknown, as verified in Feb 2024. You cannot join it, but the record below documents what was studied.

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