- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06243341
The Impact of MACA Supplementation on Basketball-related Performance
February 1, 2024 updated by: Chih-Hui Chiu, National Taiwan Sport University
The Impact of Lepidium Meyenii (MACA) Supplementation on Basketball-related Performance and Anti-fatigue Ability: a Double Blind Crossover Study
In this randomized crossover study, ten elite healthy male basketball players were included.
Following a 17:00 PM training routine, participants completed a two-week supplementation with 2000 mg of MACA or placebo.
After supplementation, participants underwent a Basketball Jump Shooting Accuracy Test and Repeated Sprint Ability Test.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Supplementation with Lepidium meyenii (MACA) has been shown in animal studies to increase blood lactate clearance and rapid lactate removal, which may be effective in reducing fatigue during intermittent exercise.
However, no studies have investigated the effects of MACA supplementation on interval exercise and basketball performance.
We hypothesized that MACA supplementation could reduce fatigue and improve performance in elite healthy male basketball players.
This study aimed to determine the effectiveness of MACA compared to placebo on overall basketball performance.
Study Type
Interventional
Enrollment (Actual)
10
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Taichung, Taiwan, 404
- National Taiwan University of Sport
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- (i) healthy male adults, those individuals who are free of pain, insomnia, or other injuries recently, without any medication used in recent 2 months,
- (ii) basketball players competing in a Taiwan university basketball association for more than two years.
Exclusion Criteria:
- (i) were below 20 years old,
- (ii) did not have won at least eighth place in national-level basketball competitions,
- (iii) were with cardiovascular diseases or any disease that made subjects feel ill.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: MACA (MC)
Daily MACA supplementation for two weeks.
|
The MACA supplement is derived from a concentrated 6:1 blend of black, red, and yellow MACA root compounds, with an 80:15:5 ratio respectively.
Other Names:
|
|
Placebo Comparator: placebo
Daily placebo supplementation for two weeks.
|
The MACA supplement is derived from a concentrated 6:1 blend of black, red, and yellow MACA root compounds, with an 80:15:5 ratio respectively.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Countermovement jump test
Time Frame: immediately after 2 weeks intervention
|
Three jumps were measured with 1 minute rest for each participant.
|
immediately after 2 weeks intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Basketball Jump Shooting Accuracy Test
Time Frame: immediately after 2 weeks intervention
|
The first test was the basketball jump shooting Accuracy Test (BJSAT), which has been used in the past with sufficient reliability to two and three-point shooting accuracy
|
immediately after 2 weeks intervention
|
|
Repeated Sprint Ability Test
Time Frame: immediately after 2 weeks intervention
|
Repeated Sprint Ability test (40× 15m with a 1:4, exercise : rest time ratio, such as 2 seconds :8 seconds)
|
immediately after 2 weeks intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Che-Hsiu Chen, PhD, Sport Science Research Center
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 1, 2022
Primary Completion (Actual)
September 30, 2022
Study Completion (Actual)
September 30, 2022
Study Registration Dates
First Submitted
January 14, 2024
First Submitted That Met QC Criteria
February 1, 2024
First Posted (Actual)
February 6, 2024
Study Record Updates
Last Update Posted (Actual)
February 6, 2024
Last Update Submitted That Met QC Criteria
February 1, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 113-1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
No personal data of participants will be provided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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