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Clinical Trials/NCT05717452
NCT05717452RecruitingNot Applicable

Effects of a Single Dose of Wild Blueberries on Mood and Executive Function in Healthy Emerging Adults: a Single-Blind, Randomized Controlled Trial

University of Reading1 site in 1 country80 target enrollmentStarted: February 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
80
Locations
1
Primary Endpoint
Positive affect as measured by PANAS-X

Study Overview

Brief Summary

This study aims to investigate whether consuming a drink containing powdered blueberries (equivalent to 150 g of fresh fruit) can improve mood and executive function in healthy emerging adults.

Detailed Description

The present study will examine the psychological effects of a single dose of freeze-dried wild blueberries using a randomized, single-blind, placebo-controlled design. A total of 80 participants will be randomly allocated to consume either a drink prepared with 22 g blueberry powder or a drink prepared with 22 g placebo powder matched for macronutrients, flavour and colour.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 25 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •18 to 25 years of age

Exclusion Criteria

  • •Any medically significant condition or mental health disorder (e.g. diabetes, endocrine or gastrointestinal disorders)
  • •Taking medication (excluding hormonal contraception or medication for asthma/seasonal allergies)
  • •Allergy to blueberries or any other Vaccinium species

Arms & Interventions

Blueberry drink

Experimental

Intervention: Blueberry drink (Dietary Supplement)

Placebo drink

Placebo Comparator

Intervention: Placebo drink (Dietary Supplement)

Outcomes

Primary Outcomes

Positive affect as measured by PANAS-X

Time Frame: 1.5 hours post-ingestion

Positive affect will be calculated by adding the values of the 21 positive items of the Positive and Negative Affect Schedule-X and the additional item "motivated". Thus, the scale will range from 0 to 88 points with higher scores indicating better mood.

Secondary Outcomes

  • Reaction time(1.5 hours post-ingestion)
  • Executive function (accuracy)(1.5 hours post-ingestion)
  • Negative affect as measured by PANAS-X(1.5 hours post-ingestion)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Prof Claire Williams

Prof. Claire Williams

University of Reading

Study Sites (1)

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