Status:

COMPLETED

PRECOG Pilot Project

Lead Sponsor:

University of Reading

Collaborating Sponsors:

Biotechnology and Biological Sciences Research Council

Myota Limited

Conditions:

Cognition

Affect (Mental Function)

Eligibility:

All Genders

60-75 years

Phase:

NA

Brief Summary

This pilot study aims to investigate the chronic effects of a prebiotic blend on cognitive, affective and gut microbiome outcomes in healthy adults aged 60-75 years.

Detailed Description

This pilot study will employ a double-blind, randomised, placebo-controlled parallel design to investigate the chronic effects of 12-week-long prebiotic blend consumption on cognitive, affective, gut ...

Eligibility Criteria

Inclusion

  • Aging between 60-75 years old
  • Having normal vision and hearing
  • Having a normal body mass index (BMI\<30)

Exclusion

  • Having mild to moderate subjective cognitive complaints
  • Smoking
  • Having food allergies
  • Following restrictive and/or unbalanced diets
  • Changing dietary intake majorly in past month
  • Being diagnosed with any psychiatric or neurologic conditions (e.g. schizophrenia, depression, dementia) including eating disorders
  • Being diagnosed with any cardiometabolic diseases (including type II diabetes and cardiovascular disease), or suffering from hypertension or thrombosis related disorders or suffer from thyroid disease
  • Currently taking anticoagulants, antiplatelet medication, antidepressants, proton-pump inhibitors
  • Currently consuming prebiotic or probiotic supplements
  • Continuous antibiotic use for \> 3 days within 1 month prior to enrolment
  • Continuous use of weight-loss drug for \> 1 month before screening
  • Having a significant gastrointestinal (GI) condition affecting absorption including (but not limited to) inflammatory bowel disease; total colectomy or bariatric surgery; irritable bowel disease; end stage renal disease; active cancer, or treatment for any cancer, in last 3 years
  • Having a high fibre intake defined as \> 20g of fibre/day
  • Wheat and/or gluten intolerance and having coeliac disease

Key Trial Info

Start Date :

May 1 2025

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 1 2025

Estimated Enrollment :

50 Patients enrolled

Trial Details

Trial ID

NCT06911957

Start Date

May 1 2025

End Date

December 1 2025

Last Update

December 3 2025

Active Locations (1)

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University of Reading, School of Psychology and Clinical Languages

Reading, Berkshire, United Kingdom, RG6 6ES