Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
The PRECOG Pilot Project is a study designed to explore how a special blend of prebiotics—a type of fiber that helps beneficial gut bacteria—affects thinking skills, mood, and gut health in healthy adults aged 60 to 75 years. If you or a family member fall within this age range, have normal vision and hearing, and maintain a healthy weight (BMI under 30), you might be eligible to participate. However, the study is not open for enrollment yet.
Participants in this trial will be asked to take the prebiotic blend and share their experiences regarding any changes in their cognitive abilities, mood, and gut health over time. It’s important to note that individuals with certain health conditions, like cognitive disorders, heart disease, or those taking certain medications, would not be eligible to join. Overall, this study aims to gather valuable information that could lead to better understanding of how gut health impacts brain function and emotional well-being in older adults.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Aging between 60-75 years old
- • Having normal vision and hearing
- • Having a normal body mass index (BMI\<30)
- Exclusion Criteria:
- • 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
About University Of Reading
The University of Reading is a prestigious research institution in the United Kingdom, renowned for its commitment to advancing knowledge across various disciplines, including health sciences. As a clinical trial sponsor, the university leverages its cutting-edge research facilities and interdisciplinary expertise to conduct innovative studies aimed at improving healthcare outcomes. With a strong emphasis on ethical research practices and collaboration with industry partners, the University of Reading strives to contribute valuable insights to the field of medicine, fostering the development of new treatments and interventions that address pressing health challenges.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Reading, Berkshire, United Kingdom
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported