An Open-label, Exploratory Study to Investigate the Efficacy of BDNF Essentials® on Cognition

Researched Nutritionals

Status and phase

Completed

Phase 1

Conditions

Cognitive Change

Treatments

Dietary Supplement: BDNF Essentials

Study type

Interventional

Funder types

Industry

Identifiers

NCT04860778

21BCHR

Details and patient eligibility

About

Full description

The objective of this open-label, exploratory study is to investigate the efficacy of BDNF Essentials® on cognition in a healthy adult population with self-reported memory complaints. As there is a dearth of available literature on BDNF in this study population, the current study is designed to understand the role of BDNF to inform potential future studies. The study population represents a target group of individuals who would benefit from safe and efficacious nutraceuticals for the support of cognitive function. This transitional stage from normal cognition to cognitive impairment is viewed as an opportune window for intervention. This population of participants is being recruited to expand on previously published work on these individual ingredients while limiting confounding variables that could influence outcomes.

Enrollment

20 patients

Sex

All

Ages

45+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Males and females 45 years of age and older
Waist circumference < 102 cm (40 inches) in men and < 88 cm (35 inches) in women
Female participant is not of child-bearing potential, defined as females who have undergone a sterilization procedure (e.g. hysterectomy, bilateral oophorectomy, bilateral tubal ligation, complete endometrial ablation) or have been post-menopausal for at least 1 year prior to enrollment

Or,

Females of child-bearing potential must have a negative baseline 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 or agrees to use contraception if planning on changing to heterosexual partner(s)
Vasectomy of partner at least 6 months prior to enrollment
- A score of ≥ 24 on the Mini-Mental State Examination (MMSE 2)
- Self-reported memory complaints as assessed by the revised Everyday Memory Questionnaire (EMQ) (with a score of ≥ 32)
- Agrees to maintain current exercise routine, sleep and dietary patterns throughout the study
- Agrees to avoid high caffeine consumption 24-hours prior to study appointments (examples include but not limited to no more than 2 cups of caffeinated coffee or tea)
- Agrees to avoid alcohol consumption 24-hours prior to study appointments
- Willingness to complete questionnaires, and diaries associated with the study and to complete all appointments
- Provided voluntary, written, informed consent to participate in the study
- Healthy as determined by medical history and laboratory results as assessed by the QI

Exclusion criteria

Women who are pregnant, breast feeding, or planning to become pregnant during the study
Allergy, sensitivity, or intolerance to the investigational product's active or inactive ingredients
Dementia and/or cognitive decline or use of prescribed medications used to for dementia and/or cognitive decline (Section 6.3.1)
Prescribed medications for depression that may affect concentration, attention and performance as assessed by the QI (Section 6.3.1)
Current use of supplements used for cognition or mood support unless on a stable dose (Section 6.3.2)
History of epilepsy, brain injury or trauma as assessed by the QI
Self-reported confirmation of sleep disorder as assessed by the QI
Prescribed or over-the-counter medications or supplements used for sleep (Section 6.3.1 and 6.3.2)
Self reported colour-blindness
Prescribed use of antibiotics within 1 month of baseline (Section 6.3.1)
Prescribed use of anticoagulants/antiplatelets (Section 6.3.1)
Prescribed or chronic use of over-the-counter anti-inflammatory medications (Section 6.3.1 and 6.3.2)
Current use of supplements containing the ingredients in the IP unless willing to washout (Section 6.3.2)
Current employment that calls for rotating shift work or shift work that will disrupt normal circadian rhythm in the last 3 weeks
Travelled across 1 or more time zones in the last 3 weeks and/or is anticipating more travel during the study
Use of medical cannabinoid products
Current chronic use of cannabinoid products (>8 times/month) and is unwilling to stop for the duration of the study beginning 1 week prior to baseline. History of chronic use and occasional use to be assessed by QI on a case-by-case basis
Use of tobacco, nicotine, or e-cigarette products within 12 weeks of baseline and during the study period
Self-reported alcohol or drug abuse within the last 12 months
Self-reported confirmation of HIV-, Hepatitis B- and/or C-positive diagnosis
Autoimmune disease including Type I diabetes or are immune compromised
Self-reported current or pre-existing thyroid condition. Treatment on a stable dose of medication for at least 3 months will be assessed by the QI
Clinically significant abnormal laboratory results at screening as assessed by the QI
Blood donation 30 days prior to enrollment, during the study, or a planned donation within 30 days of the last study appointment
Participation in other clinical research studies 30 days prior to enrollment will be assessed on a case-by-case basis by the QI
Individuals who are unable to give informed consent
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