- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03923608
Reliability of a Endurance and a Strength Test for Shoulder Rotation
Localized Muscle Resistance Test: Identification and Use of Parameters for Prescription of Exercise Resisted in Different Evaluation Tools
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
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São Paulo
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Presidente Prudente, São Paulo, Brazil, 19060-900
- State University of são Paulo
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria: should report the absence of:
- anemia,
- diabetes,
- cardiovascular disease,
- and upper limb and spinal muscular injuries in the last six months
Exclusion Criteria:
- absence at any study session and
- episode of muscle-tendon or osteoarticular injury in the upper limbs during the study.
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
strength test
The maximum strength test of external shoulder rotators will be performed on 5 different tools with specific protocols.
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1RM test performed in 5 different tools (Elastic Band, Pulley, halter, digital dynamometer and isokinetic dynamometer)
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Endurance test
Test designed by the Laboratory of Sports Physical Therapy (LAFIDE) of FCT / UNESP - Presidente Prudente, used in the prescription of training for gain of localized muscular endurance. Will be realized in the tools: Isokinetic dynamometer, elastic bands, pulley and halter. The test will consist of the maximum possible repetitions (until fatigue) with loads of 70%, 80% and 90% of the maximum force (in different sessions). |
Test performed until individual exhaustion in 5 different tools (Elastic Band, Pulley, halter and isokinetic dynamometer)
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Maximal force (kilograms)
Time Frame: Stage 1 - 0 minutes after strength test
|
The maximum force of the participant shall be measured with the values presented in kilogram
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Stage 1 - 0 minutes after strength test
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Time (seconds)
Time Frame: Stage 2 - 0 minutes after Endurance test
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Stage 2 - 0 minutes after Endurance test
|
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Number of repetitions
Time Frame: Stage 2 -0 minutes after Endurance test
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Stage 2 -0 minutes after Endurance test
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Anthropometric evaluation
Time Frame: Stage 1 - 10 minutes before stregth test
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To determine the value corresponding to the body mass, the volunteers will be evaluated by a digital scale (Tanita BC554, Iron Man / Inner Scaner - Tanita, Illinois, United States).
Stature values will be obtained by means of a stadiometer (Sanny - American Medical do Brasil, São Paulo, Brazil).
From these values it will be possible to calculate the Body Mass Index (BMI), determined by the ratio of weight to height squared.
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Stage 1 - 10 minutes before stregth test
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Psychological Questionnaire
Time Frame: Stage 1 - 10 minutes before stregth test
|
The questionnaire aims to subjectively document physical and metal readiness scores for exercise, fatigue, vigor, drowsiness, and muscle pain.
Participants will be instructed to mark a dash on a visual analogue scale of 10 centimeters between two extremes, zero being "least possible" and 10 indicating "most possible" for each classification60.
This questionnaire will be applied at the beginning of all sessions.
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Stage 1 - 10 minutes before stregth test
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International Physical Activity Questionnaire (IPAQ)
Time Frame: Stage 1 - 10 minutes before stregth test
|
The IPAQ questionnaire is an instrument developed to estimate the level of habitual practice of physical activity.
Sedentary - Does not perform any physical activity for at least 10 continuous minutes; Insufficiently Active - Individuals who engage in physical activity for at least 10 continuous minutes per week, but insufficiently to be classified as active.
A) Perform 10 continuous minutes of physical activity, following at least one of the following criteria: frequency - 5 days/week or duration - 150 minutes/week; B) Does not meet any of the criteria of the recommendation cited in under-active individuals A; Active - a) vigorous physical activity - ≥ 3 days/week and ≥ 20 minutes/session; b) moderate or walking - ≥ 5 days/week and ≥ 30 minutes/session; c) any added activity: ≥ 5 day/week and ≥ 150 min/week; Very Active - a) vigorous - ≥ 5 days/week and ≥ 30 min/session; b) vigorous - ≥ 3 days/week and ≥ 20 min/session + moderate and or ≥ 5 days/week and ≥ 30 min/session.
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Stage 1 - 10 minutes before stregth test
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Borg's Perception of Effort Scale
Time Frame: Stage 2 - 0 minutes after endurance test in all tools
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The degree of subjective effort reported by the participants in relation to the upper limbs will be analyzed using the Borg scale of perception of effort of 6 to 20 points, 6 corresponding to the "very easy" and 20 to "exhaustive".
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Stage 2 - 0 minutes after endurance test in all tools
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Perceived effort
Time Frame: Stage 2 - 0 minutes after endurance test in all tools
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The perceived exertion of the resisted exercise will be evaluated through the OMNI Resistance Exercise Scale for Perceived Effort62,63, which consists of an ordinal scale of 0 to 10, 0 being extremely easy and 10 extremely difficult.
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Stage 2 - 0 minutes after endurance test in all tools
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Recovery Perception
Time Frame: Stage 2 - 10 minutes after endurance test in all tools
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The perception of recovery of the dominant lower limb will be evaluated through the Likert Scale of Recovery Perception, which consists of a scale with values between 1 and 10 points, 1 corresponding to no recovery and 10 to fully recovered
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Stage 2 - 10 minutes after endurance test in all tools
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Participation of the anaerobic parameter
Time Frame: Stage 3 - During endurance test, until 7 minutes after test
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The total participation of the anaerobic parameter (PANA) will be calculated by the sum of the lactary anaerobic (CLAC) and alactic (CALA) contributions, analyzed by [lac] and the excess of post-exercise oxygen consumption (EPOC), respectively.
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Stage 3 - During endurance test, until 7 minutes after test
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Carlos Marcelo Pastre, PhD, Universidade Estadual Paulista Júlio de Mesquita Filho
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- SP-Unesp
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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