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Investigation of the Effects of Longvida Curcumin on Cognitive Function, Mood and Biomarkers of Health.

Phase 3
Active, not recruiting
Conditions
Cognitive function
Psychological wellbeing (mood, stress fatigue, sleep)
Cardiovascular function
Brain function (fMRI)
Inflammation
Oxidative Stress
Mental Health - Studies of normal psychology, cognitive function and behaviour
Alternative and Complementary Medicine - Herbal remedies
Neurological - Studies of the normal brain and nervous system
Registration Number
ACTRN12616000484448
Lead Sponsor
Swinburne University of Technology, Centre for Human Psychopharmacology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Active, not recruiting
Sex
All
Target Recruitment
80
Inclusion Criteria

1.Aged 50-85 years.
2.Willing and able to provide written informed consent.
3.Understand and willing and able to comply with all study procedures.
4.No history of stroke, neurological conditions (e.g. Parkinson’s, epilepsy), depression, psychiatric disorders, low base line intellect, alcohol abuse past / present.
5.Free from dementia.
6.Fluent in written and spoken English.
7.Must have normal or corrected vision and not colour blind.
8.Free from medical conditions which may affect ability to participate in the study
9.Participants taking part in the MRI sub-study must be right handed

Exclusion Criteria

1.Any significant concurrent illness including any auto-immune disorder, bleeding disorders, currently impaired cardiovascular function, Type I diabetes, glaucoma, uncontrolled high blood pressure or gallstones.
2.Any known or suspected food allergies
3.Smokers and users of recreational drugs (except alcohol and other food grade actives).
4.Have participated in any other study involving an investigational product in the last 4 weeks.
5.Taking anti-coagulant drugs or anti-cholinergics or acetylcholinesterase inhibitors.
6.Taking steroid medications.
7.Taking vitamins or herbal supplements that are reasonably expected to influence study measures.
8.Left-handed participants will be ineligible to take part in the MRI sub-study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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