The Cognitive Effects of 6- and 12-weeks Administration of a Food Supplement Containing Phosphatidylserine in Healthy Children Aged 8 to 12 Years
Launched by NORTHUMBRIA UNIVERSITY · Dec 15, 2021
Trial Information
Current as of September 28, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Participants must be in good health as reported by themselves and their parent/guardian.
- • Healthy children aged 8 to 12 years and enrolled in school years 4 to 7 at the time of giving consent
- • Have been speaking English at school since reception
- • Willingness of the children and parents to give their written informed consent, according to GCP and local regulations and being able to participate in all scheduled visits, intervention plans, tests and other trial procedures
- • Children with a normal sex and age-related BMI according to the local NHS guidelines (3rd to 90th percentiles)
- Exclusion Criteria:
- • Relevant allergy or known hypersensitivity to one of the ingredients contained in the investigational drug.
- • Are currently taking any illicit, herbal or recreational drugs including alcohol and tobacco.
- • Taking any prescribed or OTC medication against chronic or non- chronic illnesses.
- • Have used dietary supplements within the last 4 weeks
- • Are diagnosed with ADHD, dyslexia or any neurodevelopmental disorder or learning difficulty.
- • Suffer from visual (including colour blindness) or hearing impairment (that may impact task performance in the opinion of the PI.
- • Have any serious illness, cognitive impairment or medical disorder that may confound with study results or interfere with compliance.
- • Have any other active or unstable medical condition, that, in the opinion of the PI, may adversely affect the participant's ability to complete the study
- • Are experiencing exceptional social/family stressors.
- • Consume more than one portion (\>100g) per week of the following dietary sources high in phosphatidylserine: Oily fish such as salmon, mackerel, herring, tuna and eel. Animal internal organs such as liver, kidney, brain and heart. Note: Information on continued adherence to this criteria will be captured within treatment diary. If a child continuously consumes more than one portion per week of PS rich food the sponsor will be informed on a case by case basis. If deemed to be significant, they will be excluded, (but allowed to continue the study to the end (day 84)) and will be replaced.
- • Subjects that have followed specific diet, e.g. high protein diet, within 30 days prior to study start
- • Serious diet change, e.g. Ketogenic or vegan, within 30 days prior to study start.
- • Consumption of \> 250 mg/day of caffeine.
- • Are unable to complete all of the study assessments
- • Are currently participating in other clinical or nutrition intervention studies, or have in the past 8 weeks
- • Are non-compliant with regards treatment consumption
About Northumbria University
Northumbria University is a leading research-intensive institution based in the UK, dedicated to advancing knowledge and innovation in various fields, including health sciences. As a clinical trial sponsor, the university leverages its academic expertise and state-of-the-art facilities to conduct high-quality research aimed at improving patient outcomes and informing clinical practices. With a commitment to ethical standards and regulatory compliance, Northumbria University collaborates with healthcare professionals and industry partners to explore novel therapeutic interventions and contribute to the body of evidence that shapes modern medicine.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Newcastle Upon Tyne, Tyne & Wear, United Kingdom
Newcastle Upon Tyne, United Kingdom
Patients applied
Trial Officials
Philippa Jackson
Principal Investigator
Northumbria University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials