Cognitive Function Clinical Trial
Official title:
Investigation of the Effects of Efalex Active 50+ on Cognitive Performance, Well-being and Cerebral Hemodynamics in Healthy Adults Aged 50-70 Years Reporting Subjective Memory Deficits
Verified date | November 2010 |
Source | Northumbria University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United Kingdom: Research Ethics Committee |
Study type | Interventional |
Dietary intake of omega-3 polyunsaturated fatty acids (n-3 PUFAs) is inversely associated
with cognitive decline and dementia (e.g. Kalmijn et al. 2004, Heude et al. 2003, Morris et
al. 2005, Dullemeijer et al. 2009). Recently, the effects of supplemental docosahexaenoic
acid (DHA) on behavioural outcomes in older adults has been explored, however two trials
addressing this issue have published conflicting results regarding the efficacy of DHA
supplementation, with one reporting a benefit of treatment on cognitive performance
(Yurko-Mauro et al. 2010), while the other did not (Dangour et al. 2010).
One area of research that has yet to be explored in this cohort is the effects of n-3 PUFAs
on brain function in physiological terms. It is also possible that n-3 PUFAs, in combination
with other compounds, may be more beneficial than treatment with n-3 PUFAs in isolation. The
current study will explore several separate hypotheses within the same cohort. These are
that Efalex Active 50+ may have a beneficial effect on:
- Cognitive performance
- Mental fatigue in response to cognitively demanding tasks
- Self-reported mood/well-being
- Task-related cerebral blood flow response
The proposed study therefore has two aims; the primary aim is to evaluate the cognitive and
mood/well-being effects of Efalex Active 50+, a dietary supplement containing a number of
potentially cognition enhancing components including DHA, phosphatidylserine, vitamin B12,
folic acid and Ginkgo biloba, compared with placebo in a sample of older adults aged 50-70
years (Cognitive Study). The second is to evaluate the cerebral haemodynamic effects of the
same treatment formulation in a sample drawn from the same population, with the addition of
a third DHA-only arm (Hemodynamics Study). The intervention period will be 6 months.
Status | Completed |
Enrollment | 261 |
Est. completion date | June 2012 |
Est. primary completion date | June 2012 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 50 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Generally healthy - Aged 50-70 years - Low consumer of oily fish (= 1 portion/month) - Has not taken vitamin/herbal supplements in the past 3 months - Has not taken omega-3 supplement (including cod liver oil) in the past 2 years - Has a good level of written and spoken English - Has an MMSE score > 24 - Is suffering from a memory complaint (MAC-Q score > 24) Exclusion Criteria: - BMI > 35 - Smokes more than 15 cigarettes per day - History of alcohol/drug abuse - Currently taking statins/antidepressant/blood thinning medication - Has high blood pressure - Suffers from migraines/anaemia/heart or lung disorder/diabetes/active infections/jaundice/haemophilia or other clotting disease - Has learning difficulties/dyslexia/colour blindness - Is HIV positive - Has hepatitis |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Basic Science
Country | Name | City | State |
---|---|---|---|
United Kingdom | Northumbria University | Newcastle upon Tyne | Tyne and Wear |
Lead Sponsor | Collaborator |
---|---|
Northumbria University | Efamol Ltd |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Cognitive performance | Performance on a number of tasks assessing cognitive function across domains (attention, memory, executive function) will be measured. | 6 months | No |
Secondary | Cerebral Hemodynamics | Cerebral blood flow response to cognitive tasks will be assessed using Near Infrared Spectroscopy (NIRS). General cerebral blood flow will be assessed using Transcranial Doppler (TCD) | 6 months | No |
Secondary | Mood/well-being | Mood and well-being will be assessed using a number of measures: Bond-Lader visual analogue scales, Profile of Mood States (POMS), General Health Questionnaire (GHQ), Pittsburgh Sleep Quality Index (PSQI) |
6 months | No |
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