Actively Recruiting

Phase Not Applicable
Age: 50Years +
All Genders
Healthy Volunteers
NCT07119788

Investigating the Effects of a Haskap Berry Supplement on Cognitive Health

Led by University of Reading · Updated on 2025-08-13

90

Participants Needed

1

Research Sites

40 weeks

Total Duration

On this page

Sponsors

U

University of Reading

Lead Sponsor

H

Haskapa Ltd

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study aims to investigate the postprandial (2h) and longer term (4 week) effects of a haskap berry supplement on cognitive, vascular, and metabolic function in healthy ageing adults aged 50+.

CONDITIONS

Official Title

Investigating the Effects of a Haskap Berry Supplement on Cognitive Health

Who Can Participate

Age: 50Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 50 years old or older
  • Fruit and vegetable intake of 4 servings or less per day
  • Ability to understand English and adequate vision and hearing to complete cognitive tests
  • Normal body mass index (BMI) for age
Not Eligible

You will not qualify if you...

  • Diagnosed psychological or psychiatric disorders
  • Attention deficit hyperactivity disorder (ADHD) or dyslexia
  • Any food allergies or intolerances
  • Use of medications or dietary supplements that may affect study results
  • Antibiotic use within the last 3 months
  • Following vegan, vegetarian, or other diets that could impact study outcomes
  • Conditions affecting nutrient absorption (e.g., celiac disease)
  • Diagnosed cardiometabolic diseases including type II diabetes and cardiovascular disease
  • Untreated hypertension or thrombosis-related disorders
  • Use of blood thinners

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Nutrition, Cognition & Health Lab, School of Psychology and Clinical Language Sciences, University of Reading

Reading, United Kingdom, RG6 6ES

Actively Recruiting

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Research Team

L

Lynne Bell

CONTACT

C

Claire M Williams

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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