The Effect of Curcumin Supplementation on Recovery From Exercise-induced Muscle Damage
NCT ID: NCT05346211
Last Updated: 2022-04-26
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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UNKNOWN
NA
36 participants
INTERVENTIONAL
2022-05-01
2023-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
BASIC_SCIENCE
DOUBLE
Study Groups
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Curcumin Single
The Single dose group will consume 1 placebo sachet and one curcumin sachet per day.
Curcumin supplementation will be from YourZooki, the supplement in question is commercially offered to the public in a tangerine flavour. The sachets will be in 750mg hydrolysed format.
The placebo is a sachet containing the same ingredients mentioned above minus the curcumin. The sachets will be in 750mg hydrolysed format.
Supplementation will be administered and commence 48-hours prior to the first testing day and will be consumed twice a day (8am \& 8pm).
Curcumin
Curcumin Supplementation
Curcumin Double
The double dose group will consume two sachets per day of curcumin.
Curcumin supplementation will be from YourZooki, the supplement in question is commercially offered to the public in a tangerine flavour. The sachets will be in 750mg hydrolysed format.
Supplementation will be administered and commence 48-hours prior to the first testing day and will be consumed twice a day (8am \& 8pm).
Curcumin
Curcumin Supplementation
Placebo
Placebo sachets containing the same ingredients mentioned above minus the curcumin. The sachets will be in 750mg hydrolysed format.
Participants will consume two sachets per day.
Supplementation will be administered and commence 48-hours prior to the first testing day and will be consumed twice a day (8am \& 8pm).
No interventions assigned to this group
Interventions
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Curcumin
Curcumin Supplementation
Eligibility Criteria
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Inclusion Criteria
* non-smoker
* no previous history of cardiovascular, respiratory, or neurological problems
* not taking anticoagulant medication
* injury-free in the 3 months prior to scheduled participation in the study
Exclusion Criteria
* any blood diseases or clotting issues,
* injury, or previous injury in \<3 months
18 Years
35 Years
ALL
Yes
Sponsors
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St Mary's University College
OTHER
Responsible Party
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Principal Investigators
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Luke Hughes, PhD
Role: PRINCIPAL_INVESTIGATOR
Northumbria University
Jess Hill, PhD
Role: PRINCIPAL_INVESTIGATOR
St. Mary's University, Twickenham
Central Contacts
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Other Identifiers
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ASE22HELCON
Identifier Type: -
Identifier Source: org_study_id
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