- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03170921
Psychophysiological Characterization of Different Capoeira Performances in Experienced Individuals
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- to be male between 18 and 40 years;
- a Capoeira practitioner for at least 2 years;
- mastering the technique of the three rhythms of performance investigated (Angola, Benguela and São Bento).
Exclusion Criteria:
- to be hypertensive, diabetic or obese;
- to be a smoker;
- alcohol addicted;
- have some cardiovascular dysfunction or musculoskeletal problem.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Angola
The rhythm performance had duration of 90 seconds.
During recovery period (post- intervention) in the moments 1, 3, 5, 7, and 9 minutes was measured the physiological and the perceptual variables of the study.
|
The rhythm performance (Angola) had duration of 90 seconds.
During recovery period (post- intervention) in the moments 1, 3, 5, 7, and 9 minutes was measured the physiological and the perceptual variables of the study.
|
Experimental: Benguela
The rhythm performance had duration of 90 seconds.
During recovery period (post- intervention) in the moments 1, 3, 5, 7, and 9 minutes was measured the physiological and the perceptual variables of the study.
|
The rhythm performance (Benguela) had duration of 90 seconds.
During recovery period (post- intervention) in the moments 1, 3, 5, 7, and 9 minutes was measured the physiological and the perceptual variables of the study.
|
Experimental: São Bento
The rhythm performance had duration of 90 seconds.
During recovery period (post- intervention) in the moments 1, 3, 5, 7, and 9 minutes was measured the physiological and the perceptual variables of the study.
|
The rhythm performance (São Bento) had duration of 90 seconds.
During recovery period (post- intervention) in the moments 1, 3, 5, 7, and 9 minutes was measured the physiological and the perceptual variables of the study.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Physiological responses (Heart rate)
Time Frame: 30 minutes
|
Heart rate (bpm) responded differently among the three investigated rhythms.
|
30 minutes
|
Physiological responses (heart rate variability)
Time Frame: 30 minutes
|
Heart rate variability indicator, R-R interval (ms), responded differently among the three investigated rhythms.
|
30 minutes
|
Physiological responses (Blood lactate)
Time Frame: 30 minutes
|
Blood lactate (mmol/L) responded differently among the three investigated rhythms.
|
30 minutes
|
Physiological responses (Blood glucose)
Time Frame: 30 minutes
|
Blood glucose (mg/dL) responded differently among the three investigated rhythms.
|
30 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Psychological responses (Rate of perceived exertion response)
Time Frame: 30 minutes
|
Rate of perceived exertion response exhibited differences when analyzed the São Bento performance in comparison to the Angola and Benguela performances in Capoeira.
|
30 minutes
|
Psychological responses (Basic affective response)
Time Frame: 30 minutes
|
Basic affective response exhibited differences when analyzed the São Bento performance in comparison to the Angola and Benguela performances in Capoeira. The Feeling Scale (FS) was used to assess the affective response and it is an 11-point bipolar scale ranging from +5 to -5, commonly used to measure pleasure/displeasure during exercise.7 This scale presents the following verbal anchors: -5 = very bad; -3 = bad; -1 = fairly bad; 0 = neutral; +1 fairly good; +3 = good; and +5 = very good. The subjects received standard instructions regarding to the use of the FS. |
30 minutes
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Other Study ID Numbers
- UFSaoFrancisco3_
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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