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NCT06790849Completed

ETASCAI Pilot Project

The Impact of Chronic Consumption of ETAS® for 12 Weeks on Cognitive, Affective, and Inflammatory Outcomes: A Randomised Parallel Group Placebo-controlled Feasibility Study

Source: ClinicalTrials.gov · Last updated 19 Nov 2025

Brief summary (registry, in English)

This pilot study aims to investigate the chronic effects of ETAS® on cognitive, affective and inflammatory outcomes in healthy adults aged 60-80 years with mild to moderate subjective cognitive complaints.

Status (registry)
Completed
Study type
Interventional
Enrollment
45 (actual)
First submitted
13 Jan 2025
Start date
24 Feb 2025
Primary completion date
22 Oct 2025
Lead sponsor
University of Reading
NCT number
NCT06790849

What you commit to

  • Study type: Interventional
  • Participants enrolled: 45
  • From 24 Feb 2025 to the primary completion date, 22 Oct 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Currently taking anticoagulants, antiplatelet medication, antidepressants, proton-pump inhibitors
  • Continuous antibiotic use for \> 3 days within 1 month prior to enrolment
  • Continuous use of weight-loss drug for \> 1 month before screening

Other illness

  • Having food allergies or intolerances
  • 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
  • Having inflammatory bowel disease; coeliac disease; total colectomy or bariatric surgery; irritable bowel disease; end stage renal disease; active cancer, or treatment for any cancer, in last 3 years

Other

  • Smoking
  • Following restrictive and/or unbalanced diets
  • Changing dietary intake majorly in past month
  • Being anaemic
  • Currently consuming prebiotic or probiotic supplements

Who the study is looking for

  • Aging between 60-80 years old
  • Having normal vision and hearing
  • Having a body mass index between 18.5 and 30
  • Having mild to moderate subjective cognitive complaints

Age in the registry: 60 years to 80 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Reading, School of Psychology and Clinical Languages
Coordinator of this site? Confirm its status
ReadingUnited KingdomUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.