Evaluating a dietary supplement for cognitive function in children
A Randomized, Triple-blind, Placebo-controlled Trial Evaluating the Efficacy of the Study Product on Overall Cognitive Function in Children
This study is testing whether a dietary supplement can help improve thinking skills in children aged 4 to 17 over 56 days.
Quick facts
| Phase | Phase 2 |
|---|---|
| Study type | Interventional |
| Enrollment | 120 (estimated) |
| Ages | 4 Years to 17 Years |
| Sex | All |
| Sponsor | SmartyPants Vitamins Inc. Industry-sponsored |
| Drugs / interventions | chemotherapy, radiation |
| Locations | 1 site (London, Ontario) |
| Trial ID | NCT06807346 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to assess the efficacy of the Kids Plus Multi & Omega dietary supplement on cognitive function in children aged 4 to 17 years over a period of 56 days. Participants will be randomly assigned to receive either the supplement or a placebo and will undergo various cognitive assessments using the NIH Toolbox Cognition Battery. The study is designed as a randomized, triple-blind, placebo-controlled trial to ensure unbiased results regarding the impact of micronutrient supplementation on cognitive performance.
Who should consider this trial
Good fit: Ideal candidates for this study are healthy children aged 4 to 17 years who are currently attending school.
Not a fit: Patients with pre-existing cognitive impairments or those not meeting the age and school attendance criteria may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance cognitive function in children through dietary supplementation.
How similar studies have performed: While there is emerging evidence supporting the positive effects of micronutrient supplementation on cognitive performance, this specific approach is still being evaluated and has limited prior success.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Males and females 4-17 years of age, inclusive 2. Females of child-bearing potential must have a negative screening urine pregnancy test and agree to use a medically approved method of birth control for the duration of the study. All hormonal birth control must have been in use for a minimum of three months. Acceptable methods of birth control include: * Hormonal contraceptives including oral contraceptives, hormone birth control patch (Ortho Evra), vaginal contraceptive ring (NuvaRing), injectable contraceptives (Depo-Provera, Lunelle), or hormone implant (Norplant System) * Double-barrier method * Intrauterine devices * Non-heterosexual lifestyle and agrees to use contraception if planning on changing to heterosexual partner(s) * Vasectomy of partner at least 6 months prior to screening * Abstinence and agrees to use contraception if planning to become sexually active during the study 3. Enrolled in and currently attending school at baseline and for the duration of the study period 4. Willing to complete evaluations, measurements, questionnaires and diaries during each clinic visit 5. Agrees to avoid eating or moderate-vigorous exercise for one hour prior to clinic visits 6. Agrees to maintain current lifestyle habits (diet, physical activity, medications, supplements, and sleep) as much as possible throughout the study and avoid taking new supplements 7. A care provider who can reliably bring the participant to all study visits; the participant's primary caregiver must be willing and able to complete the questionnaires as needed for all visits 8. The child and the child's parent(s) or legal guardian(s) have given voluntary, written, informed assent and consent, respectively, for their child to participate in the study 9. Healthy as determined by medical history as assessed by Qualified Investigator (QI) Exclusion Criteria: 1. Individuals who are pregnant, breast feeding, or planning to become pregnant during the study 2. Allergy, sensitivity, or intolerance to the investigational product or placebo ingredients 3. Previous diagnosis or treatment of a significant neuropsychological condition and/or cognitive impairment (e.g., Schizophrenia, bipolar disorder, post-traumatic stress disorder, brain injury, neurodegenerative disease, infections, insomnia, depression, epileptic or other seizure-related disorders) that could interfere with study participation as assessed by the QI 4. Unable to communicate or cooperate due to language problems, learning disability, poor mental development, or impaired cerebral functions as assessed by the QI 5. Previous diagnosis of Attention-deficit hyperactivity disorder (ADHD) 6. Previous diagnosis of visual (including color blindness/weakness) or hearing impairment that may impact task performance as assessed by the QI 7. Currently experiencing major social/family stressors as confirmed by the child's parent or legal guardian (s) 8. History or presence of a clinically relevant cardiac, renal, hepatic, endocrine (including diabetes mellitus), pulmonary, biliary, gastrointestinal condition which affects absorption, or pancreatic disorders, as assessed by the QI 9. Cancer, except skin basal cell carcinoma completely excised with no chemotherapy or radiation with a follow up that is negative. Volunteers with cancer in full remission for more than five years after diagnosis are acceptable 10. Individuals with an autoimmune disease or are immune compromised 11. Use of cannabinoid, tobacco or nicotine-containing products, or alcohol consumption 12. Alcohol or drug abuse within the last 12 months 13. Current use of prescribed and/or over-the-counter (OTC) medications, supplements, and/or consumption of food/drinks that may impact the efficacy of the investigational product (Sections 7.3.1 and 7.3.2) 14. Employees/children of employees of study sponsor or research organization 15. Participation in other clinical research studies 30 days prior to baseline, as assessed by the QI 16. Parent or guardian who are unable to give informed consent 17. Any other condition or lifestyle factor, that, in the opinion of the QI, may adversely affect the participant's ability to complete the study or its measures or pose significant risk to the participant
Where this trial is running
London, Ontario
- KGK Science Inc. — London, Ontario, Canada (Recruiting)
Study contacts
- Study coordinator: Erin Lewis, PhD
- Email: elewis@kgkscience.com
- Phone: 1-226-242-4551
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.