Seaweed Extract Supplementation and Metabolic Biomarkers
NCT ID: NCT03853343
Last Updated: 2022-03-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
10 participants
INTERVENTIONAL
2018-06-28
2022-01-30
Brief Summary
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Detailed Description
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Seaweed have traditionally been consumed as a readily available whole food or traditional medical preparations, especially in Asia. Seaweeds are rich in bioactive compounds in the form of polyphenols, carotenoids, vitamins, minerals, phycobilins, phycocyanins, and polysaccharides, many of which are known to offer a wide range of benefits in human health.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
QUADRUPLE
Study Groups
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Placebo
3 capsules per day (1 before each meal) of cellulose
Placebo
1 capsule 3 times per day
Seaweed extract
3 capsules per day (1 before each meal) of seaweed extract
Seaweed extract
1 capsule 3 times per day
Interventions
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Seaweed extract
1 capsule 3 times per day
Placebo
1 capsule 3 times per day
Eligibility Criteria
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Inclusion Criteria
* Not dieting within the last month and not having lost \>5% body weight in the previous year
* Not increased physical activity levels in the past 2-4 weeks or intending to modify them during the study
* Understands and is willing, able and likely to comply with all study procedures and restriction including being willing to follow the nutritional advice
* Able to eat most everyday foods
* Habitually consumes three standard meals a day
Exclusion Criteria
* Taking any medication or supplements known to affect mineral or glucose metabolism within the past month and/or during the study
* Pregnant, planning to become pregnant or breastfeeding
* History of anaphylaxis to food
* Known allergies or intolerance to foods and/or to the study materials (or closely related compounds) or any of their stated ingredients
* BMI \<25 kg/m2 or \>35 kg/m2
* Volunteers self-reporting currently dieting or having lost \>5% body weight in the previous year
* Participants with abnormal eating behaviour
* Participation in another experimental study or receipt of an investigational drug/product within 30 days of the screening visit
* Volunteers who have significantly changed their physical activity in the past 2-4 weeks or who intend to change them during the study
* Participants receiving systemic or local treatment likely to interfere with the evaluation of the study parameters
* Participants on specific food avoidance diets
* Participants who work in appetite or feeding related areas
18 Years
65 Years
ALL
Yes
Sponsors
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University of Roehampton
OTHER
BioAtlantis Ltd.
INDUSTRY
Responsible Party
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Dr. George Tzortzis
Principle Investigator Human Health
Principal Investigators
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George Tzortzis
Role: STUDY_DIRECTOR
BioAtlantis Ltd.
Locations
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Roehampton University
London, , United Kingdom
Countries
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Other Identifiers
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BioAtlDG001
Identifier Type: -
Identifier Source: org_study_id
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