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NCT04647019: BluMood

The Effects of Wild Blueberries on Depressive Symptoms in Young Adults

Completed NA Last updated 31 January 2023
What this trial tests

NA trial testing Wild blueberry powder in Depression in 62 participants. Completed in 11 June 2022.

Timeline
26 November 2021
Primary endpoint
11 June 2022
11 June 2022

Quick facts

Lead sponsorUniversity of Reading
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment62
Start date26 November 2021
Primary completion11 June 2022
Estimated completion11 June 2022
Sites1 location across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

University of Reading

Who can join

Adults 18 to 24, any sex, with Depression or Anxiety. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study aims to investigate the effects of a 6-week dietary intervention of 22 g freeze-dried whole wild blueberry powder. The outcomes include measures of depression, anxiety, anhedonia, cognitive function, and biomarkers of inflammation and oxidative stress.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. A biphasic response to blueberry supplementation on depressive symptoms in emerging adults: a double-blind randomized controlled trial.
    Velichkov M, Bezur Z, van Reekum CM, Williams CM. · · 2024 · cited 8× · PMID 38300292 · DOI 10.1007/s00394-023-03311-9

Verify or expand the search:

Other trials of Wild blueberry powder

Trials testing the same drug.

Other recruiting trials for Depression

Currently open trials in the same condition.

Other University of Reading trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04647019.

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