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DepressionNCT06936202

Effects of Spirulina Supplementation on Mental Health in Healthy Adults

A study testing Spirulina capsules in people with Depression and Mental Acuity, run by Arizona State University at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

Spirulina platensis is a form of cyanobacteria, a blue-green algae, and is a superfood most known for being rich in protein, vitamins and minerals, and healthful phytochemicals. Spirulina supports brain health through neuroprotection offered by its antioxidants, anti-inflammatory properties, and hormone regulation. Read more about this study

Who is it for?
Ages 16 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Depression, Mental Acuity
What is being tested?
Spirulina capsules
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
30 participants
Where
1 siteUnited States
Study dates
15 Apr 2025to May 2026
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 16 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • healthy adults
  • ages 18-65
  • no underlying chronic disease or acute conditions
  • no autoimmune conditions
  • do not consume alcohol in excess, smoke, use recreational drugs
  • does not follow restrictive diets
  • will be recruited from the ASU university campus.

Who cannot join

  • not have been clinically diagnosed with depression
  • not taking antidepressants, anxiety, or stress medications, or any other medications
  • drugs, or supplements that could influence mental capacities
  • not pregnant or breastfeeding
  • not a competitive athlete

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Carol Johnston, PhD contact

16024962539

carol.johnston@asu.edu

United States1 site, 1 recruiting
  • 850 PBC

    Phoenix, Arizona, 85004

    Carol Johnston, 602-496-2539, carol.johnston@asu.edu

    Recruiting

Other trials in United States

About this study

Spirulina platensis is a form of cyanobacteria, a blue-green algae, and is a superfood most known for being rich in protein, vitamins and minerals, and healthful phytochemicals. Spirulina supports brain health through neuroprotection offered by its antioxidants, anti-inflammatory properties, and hormone regulation.

The aim of this study is to supplement healthy adults from a campus community with 3g of spirulina, daily, for 8 weeks to improve mood and mental acuity in comparison to receiving a placebo.

Read the detailed description

Spirulina is nutrient-dense with vitamins and minerals which provide antioxidants and anti-inflammatory mechanisms to help reduce oxidative stress and ROS activity. Preclinical studies have indicated Spirulina can reduce inflammatory cytokines, such as IL-1β, and reverse stress responses and oxidative damage in BDNF, nuclear factor erythroid 2-related factor (NRF2), and ultimately the phosphorylation of protein-kinase B (AKT), which promotes cell growth. In addition to these benefits, fatty acids, gamma-linolenic acid (GLA) and glycolipids, support gut health and the immune system. In combination, all these nutrients help increase neuroprotection and brain health.

It is evident that Spirulina supports brain health through neuroprotection, antioxidants, anti-inflammatory properties, and hormone regulation. Research supports Spirulina reversing neurodegenerative diseases due to several of these beneficial properties. There have been many studies that utilize Spirulina to improve cognitive function in Alzheimer's Disease, Parkinson's Disease, ulcerative colitis, IBD, fibromyalgia and even in TBI and Ischemic stroke.

Although many of these diseases have depressive symptoms, few of these studies have evaluated the impact of Spirulina on mood. Furthermore, no studies have been conducted relating depression and the cyanobacteria. It is possible that Spirulina supplements can be used to reduce feelings of hopelessness and lack of energy, by providing additional vitamins, minerals, amino acids, and fatty acids, on a daily basis. This study aims to compare spirulina and its improvement on mood, in health college students, by daily supplementation of 3g of Spirulina over a span of 8 weeks.

Being tested
Spirulina capsules, Placebo
Keywords
spirulina, depression, mental acuity
Medical subject headings
Depression

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Spirulina capsulesOther

    active intervention

  • PlaceboOther

    no active ingredient

Study groups in NCT06936202
Study groupRoleWhat they receive
spirulina capsulesExperimentalsix capsules daily (totaling 3 g)
Receives: Other: Spirulina capsules
PlaceboPlacebo comparatorPea powder - 6 capsules daily
Receives: Other: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. POMS (profile of mood states questionnaire)

    A validated measure consisting of 65 brief phrases, asking how they have personally felt over the last week, including today. The participants were asked to carefully rate their response on a 5-point Likert scale, ranging from 'not at all' to 'extremely'.

    Measured: conducted at baseline and at week 8 (study's end)

  2. Trail Making Test

    The TMT consists of two iterations - versions A and B - and brief samples of each will be provided for the participant to practice prior to the longer, scored version. This is a timed paper and pencil test requiring the participant to connect a series of numbers and/or letters that are randomly arranged.

    Measured: conducted at baseline and at week 8 (study's end)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Apr 2025
  2. Study start15 Apr 2025
  3. Primary completionMay 2026 (estimated)
  4. Study completionMay 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Model description
This is a parallel arm, 8-week, randomized controlled study with an experimental arm and a control arm.
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06936202
Sponsor's protocol ID
STUDY00021993
Status last verified
Aug 2025
First submitted
12 Apr 2025
Last updated
19 Aug 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: We do not plan to publish in ICMJE journals

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