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The Efficacy of Chlorella Supplementation on Health and Performance Following a 12-week Training Programme

The Efficacy of Chlorella Supplementation on Health and Performance Following a 12-week Training Programme

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05639634
Enrollment
36
Registered
2022-12-06
Start date
2023-01-11
Completion date
2023-09-23
Last updated
2024-01-31

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

Conditions

Overweight, Sedentary

Brief summary

Algae are an emerging functional food source that are gaining traction and popularity in biopharmaceutical, nutraceutical, and biotechnology industries. They are a diverse and complex species that comprise an abundant breadth of micronutrients (multiple vitamins, minerals, fatty acids, and amino acids) that can possibly promote human health. One such popular algae is chlorella, a unicellular dark green organism, which can be readily bought in health stores worldwide. Although there is some promising data to suggest chlorella supplementation can alleviate cardiovascular risk factors and improve VO2max from supplementation alone, an area which has particularly limited existing literature is the possible ergogenic and health influence of chlorella supplementation combined with a controlled training programme in sedentary and overweight populations. Given that such populations are susceptible to increased risk of developing associated diseases (cardiovascular disease, diabetes, hypertension) and possess poor diets, there is a need to investigate the possible synergistic effect of a training programme and supplementation of algae further. Furthermore, there is growing evidence to suggest that supplementation with algae may have a beneficial effect on cognitive function, primarily owed to antioxidant and anti-inflammatory mechanisms. Therefore, the purpose of this study aims to assess the efficacy of chlorella supplementation on VO2max, blood lipid profiles, cognitive function and body composition following a 12-week training programme. Briefly, in a double blind, randomised, placebo-controlled trial, participants will be randomly allocated into 1 of 4 groups (A. Exercise + Chlorella, B. Exercise + Placebo, C. Control + Chlorella, D. Control + Placebo).

Interventions

DIETARY_SUPPLEMENTChlorella supplementation

Supplementation with Chlorella (1.5 g/d) in 3 capsules for 12 weeks.

OTHER12 week cardiovascular training programme

Participants will be asked to complete a 12 week cycling training programme. This will consist of 4 X 50 min sessions per week. Each exercise session will include a warm-up phase (\ 5 min), a main physical conditioning phase (\ 40 min), and a cool-down phase (\ 5 min).

DIETARY_SUPPLEMENTPlacebo Supplementation

Supplementation with Placebo - microcrystalline cellulose (1.5 g/d) in 3 capsules for 12 weeks.

Sponsors

University College, London
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Masking description

Double

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged 18-50 * Classified a sedentary (\<30 minutes of moderate intensity exercise for \<3 days per week for 3 months) and/or overweight (BMI = 25 +) * Be willing to complete a 12-week training programme

Exclusion criteria

* Individuals taking blood thinners. * Known allergies to algae/mould and iodine. * Taking immunosuppressant medication * Regularly ingesting algae * Smokers

Design outcomes

Primary

MeasureTime frameDescription
Changes in cardiovascular fitness (VO2max)At baseline, week 6 and at week 12Changes in cardiovascular fitness variables as measured by a Cardio Pulmonary Exercise Test.
Changes in blood lipid profilingAt baseline, week 6 and at week 12Assessing changes in blood lipids (Triglycerides, cholesterol, low-density lipoprotein, High-density lipoprotein)

Secondary

MeasureTime frameDescription
Changes in cognitive function (endogenous and exogenous attending)At baseline, week 6 and at week 12 (before and after exercise)Assessing changes in endogenous and exogenous attending (m/s & number of errors) using the Gorilla Experiment Builder on a laptop.
Changes in cognitive function (context memory)At baseline, week 6 and at week 12 (before and after exercise)Assessing changes in source and context memory (m/s & number of errors) using the Gorilla Experiment Builder on a laptop. spatial anticipation
Changes in cognitive function (spatial anticipation)At baseline, week 6 and at week 12 (before and after exercise)Assessing changes in spatial anticipation (m/s & number of errors) using the Gorilla Experiment Builder on a laptop.
Changes in body composition variablesAt baseline, week 6 and at week 12Assessing changes in body composition variables using the Tanita. Weight (kg) and height (cm) will be combined to report BMI in kg/m\^2.
Changes in body composition variables (fat & lean mass percentage)At baseline, week 6 and at week 12Assessing changes in body fat mass (Body Fat mass %) and lean mass in percentage (Lean mass %) using the Tanita.
Changes in body composition variables (fat free and muscle mass)At baseline, week 6 and at week 12Assessing changes in fat free mass (kg) and muscle mass (kg) using the Tanita.
Changes in blood pressureAt baseline, week 6 and at week 12Assessing changes in blood pressure (mmHg). Systolic and diastolic, using the ABP-Monitor Mobil-O-Graph NG
Changes in cognitive function (simple reaction time)At baseline, week 6 and at week 12 (before and after exercise)Assessing changes in simple reaction time (m/s & number of errors) using the Gorilla Experiment Builder on a laptop.
Changes in total vascular resistanceAt baseline, week 6 and at week 12Assessing changes in total vascular resistance (TVR) using the ABP-Monitor Mobil-O-Graph NG.
Changes in augmentation indexAt baseline, week 6 and at week 12Assessing changes in augmentation index (Alx) using the ABP-Monitor Mobil-O-Graph NG.
Changes in augmentation pressureAt baseline, week 6 and at week 12Assessing changes in augmentation pressure using the ABP-Monitor Mobil-O-Graph NG.
Changes in lactateAt baseline, week 6 and at week 12Assessing changes in lactate at rest, peak, +5mins post, +10mins post, +30mins post
Changes in biomarkers for brain healthAt baseline, week 6 and at week 12Assessing changes in Brain-Derived Neurotrophic Factor (before exercise at rest and 30-mins post peak exercise)
Changes in Nitrate/NitriteAt baseline, week 6 and at week 12Assessing changes in plasma Nitrate and Nitrite concentrations
Changes in pulse wave velocityAt baseline, week 6 and at week 12Assessing changes in pulse wave velocity (PWV) using the ABP-Monitor Mobil-O-Graph NG.
Changes in cognitive function (inhibition)At baseline, week 6 and at week 12 (before and after exercise)Assessing changes in inhibition (m/s & number of errors) using the Gorilla Experiment Builder on a laptop.

Countries

United Kingdom

Outcome results

None listed

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