- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03522883
Pre-Competition Carbohydrate Supplementation
Acute Effects of Previous Carbohydrate Intake on Perceived Exertion and Muscle Strength in Jiu-jitsu Athletes
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The study will be conducted at the "Team Base" training center, located in the western zone of Rio de Janeiro. All procedures were performed under standard conditions (temperature: 21-23 ° C, relative humidity: 40-60%). Participants were previously instructed not to perform vigorous exercise 24 hours prior to data collection and to fast 8 hours prior.
All procedures will be performed in one day. Before the study procedures, participants will be evaluated for anthropometric characteristics using a scale (GAMA ITALY® brand) and a portable stadiometer (Sanny® brand, Personal model). Then, manual palmar grip strength (FPM) will be measured in pre and post fight moments. And, after the fight will also be verified the participants' perception of effort through the adapted Borg scale.
Procedures Fights The struggles (Handori) began respecting the schedules stipulated between the components of the same group. Thus, each fight lasted five minutes, without intervals, where the athletes were instructed to perform dynamic movements, and maintain high movement, aiming to raise the intensity to the maximum during this period.
Carbohydrate Supplementation For the administration of carbohydrate supplementation, the "Advanced Nutrition®" pack containing 30g (1 sachet), energy of 83kcal = 349kJ, carbohydrates 21g, sodium 82mg, vitamin C 4, 2mg and vitamin E 0.90mg.
Palmar Manual Holding Force (FPM) Measurement of the Manual Holding Force (FPM) was performed using the JAMAR® analog hydraulic dynamometer (Asimow Engineering®, USA), with an accuracy of 0.5 kg / f and a maximum capacity of 100 kg / f. Thus, the position suggested by the American Society of Hand Therapists (ASHT) [8] was used, with the participants positioned in a seated position with their hips and knees at 90 ° flexion, shoulder in adduction, elbow flexed at 90 °, wrist and forearm in neutral position. The participant was instructed to perform the greatest possible force and the peak value was subsequently recorded.
Modified Borg Scale Perceived exertion was assessed using the Adapted BORG Scale [7] consisting of an ordinal scale ranging from 0 to 10, where 0 represents none and 10 represents maximum intensity. The following standardized question preceded the application of the scale: "How do you rate the intensity of the exercise performed?" Statistical analysis Mean and standard deviation values were calculated for all variables. The normality of the data was initially analyzed by the Komolgorov-Smirnov procedure. In addition, t-test was used to compare moments and groups. All statistical analysis assumed a significance level of 5%. The analyzes were conducted using the statistical package SPSS (2.0).
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Jaqueline Silva
- Phone Number: + 55 66 990202206
- Email: jaqueee-santosss@hotmail.com
Study Contact Backup
- Name: Jaqueline Silva
- Phone Number: + 55 66 999202206
- Email: jaqueee-santosss@hotmail.com
Study Locations
-
-
Sao Paulo
-
Presidente Prudente, Sao Paulo, Brazil, 19060-900
- Recruiting
- Ary
-
Contact:
- Aryane Machado
- Phone Number: 18981071088
- Email: ary_machado@hotmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- healthy young people;
- Male, aged 20-45 years, professional jiu jitsu athletes;
Exclusion Criteria:
- musculotendinous lesion or osteoarticular lesion;
- people who take anabolic steroids
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Placebo Comparator: group control
the subjects will not take any type of nutrient intake
|
Participants will be submitted to carbohydrate supplementation prior to exercise
|
Experimental: experimental group 1
carbohydrate intake prior to exercise
|
Participants will be submitted to carbohydrate supplementation prior to exercise
|
Active Comparator: experimental group 2
carbohydrate intake prior to exercise
|
Participants will be submitted to carbohydrate supplementation prior to exercise
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
muscle strength
Time Frame: five minutes
|
the muscular force will be measured by means of a manual dynamometer in the dominant upper limb in two moments (pre-fight and post-fight)
|
five minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Perception of effort
Time Frame: five minutes
|
The perception of effort will be measured through a validated scale (BORG), in the moment after competition.
It is a graded scale from 0 to 10 that classifies the individual's perception of effort related to the activity performed.
|
five minutes
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- SaoPSU_UFMT
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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