- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT03373747
Reliability and Physiological Analysis of an Isometric Test of Localized Muscular Fatigue
Reliability Intra and Inter-evaluators and Physiological Analysis of an Isometric Test of Localized Muscular Fatigue
Introduction: The isokinetic dynamometer, considered a gold standard tool for physical evaluation, is widely used in studies that aim to evaluate the reliability and reproducibility of localized muscular endurance (LME) tests. However, such tests may not represent full LME by fixing time or number of replicates. Therefore, it is relevant to construct a test that respects the actual capacity of each subject to withstand fatigue and to submit such a test to validation, as well as to physiological analysis.
Research objectives: To assess the inter- and intra-rater reliability of a localized isometric endurance test (IET) on the isokinetic dynamometer and to establish the metabolic demand required during the test.
Design: Reliability study with test-reteste dynamic.
Participants and Setting: After fulfilling the eligibility criteria, eighty-eight male participants will participate in the study.
Procedure: In phase 1 forty-eight participants will submitted to reliability of the IET within three sessions: familiarization session, test session and retest sessio. In phase 2 forty participants will be submitted the metabolic demand required during the IET will be analyzed by means of gas analysis, blood lactat concetrate and muscular activation percentage.
Intervention: isometric endurance teste.
Measurements: The measurements include time of execution of test, work of test, physiological and psychological outcomes.
연구 개요
상세 설명
Introduction: The isokinetic dynamometer, considered a gold standard tool for physical evaluation, is widely used in studies that aim to evaluate the reliability and reproducibility of localized muscular endurance (LME) tests. However, such tests may not represent full LME by fixing time or number of replicates. Therefore, it is relevant to construct a test that respects the actual capacity of each subject to withstand fatigue and to submit such a test to validation, as well as to physiological analysis.
Research objectives: To assess the inter- and intra-rater reliability of a localized isometric endurance test (IET) on the isokinetic dynamometer and to establish the metabolic demand required during the test.
Design: Reliability study with test-reteste dynamic.
Participants and Setting: After fulfilling the eligibility criteria, eighty-eight male participants will participate in the study. The inclusion criteria include: healthy male, aged between 18-30 years who agree to participate in the study. Participants with the following will be excluded from the study: presence of anemia, inflammation, being sick, training or physical activity at least 24 hours prior the application of the test, being influenced in some way by test information, do not understand the teste and occurrence of musculoskeletal injury during the study.
Procedure: In phase 1 forty-eight participants will submitted to reliability of the IET within three sessions: familiarization session, test session and retest sessio. In phase 2 forty participants will be submitted the metabolic demand required during the IET will be analyzed by means of gas analysis, blood lactat concetrate and muscular activation percentage.
Intervention: This is a test that was developed by the Laboratory of Sports Physiotherapy of FCT/UNESP - Presidente Prudente. The test will be performed on the Biodex System Pro 4 isokinetic dynamometer (Biodex Medical System, Shirley-NY, USA). At first, participants will be be positioned and fixed on the device itself by their trunk, hips, thighs and by the distal region of the assessed lower limb (dominant). The protocol is composed by a 10 knee flexo-extension warm up at the speed of 330º/s, respecting the amplitude of 90º, then a 30 second isometric contraction from 50% to 60% of the maximum participant effort, according to the Effort Perception Scale. The test starts after two minutes of rest. So that it can take place, participants will be instructed to make as much effort as possible, according to the same scale, for as long as possible, until they can't keep muscle contraction no longer. To stimulate participants, evaluators will offer verbal motivation and they will follow a monitor, coupled to the device, which offers the power generation line which works as a visual feedback during all test long.
In phase 1, the first of familiarization is to the participants understand the test and familiarize with the equipment after 24 to 48 hours, the participants will do the test applied twice at the same day with 10 minutes of rest. For realization of the IET the participants will be instructe to make the maximum effort as possible and mantain until they can't resiste. After one week the retest session will be doing. The order between the evaluators will be changed in the test and retest sessions. In phase 2, the participants will be submitted two sessions, familiarization session and test session. In the test session there is be two teste applied in the same day with approximately 20 minutes of rest. In the first test, thers is gas analysis during all the test until seven minutes after the test and blood lactat concentrate will be colected before the test with 10 minutes of rest, immediately after the teste and in the first, in the third, fifth and seventh minutes after the test. In the second test will be assess the muscular activation porcentage of lateral vastus muscle by means of twitch interpolation technique there is be performe before and after the test.
Measurements: The measurements include time of execution of test (in seconds), work of test (in N.m), physiological (gas analysis, blood lactate concentration, muscular activation percentage) and psychological outcomes (Psychological Questionnaire, Work Ability Index Questionnaire, Perceived Stress Scale, The Bergen Insomnia Scale, Need for Recovery Scale, The Borg Scale, The Borg CR10 Scale, The Effort Perception Scale and Recovery Perception Scale) and clinical outcomes (heart rate).
Analysis: To analyse the normality will be used Shapiro Wilk test. For analysis of reliability test-retest will be used the intraclasse correlation coefficient (ICC), with confidence interval of 95% to reliability relative. To assess the reliability absolute the typical error and coefficient of variation will be done. The paired test t will be do to verify diferences n the mean of the groups. The psychological outcomes wiil be done with correlation and linear regression as well the physiologica outcomes. A significance level of 5% will be assumed for all statistical analysis.
연구 유형
등록 (실제)
단계
- 해당 없음
연락처 및 위치
연구 장소
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-
SP
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Presidente Prudente, SP, 브라질, 19060-900
- Larissa Rodrigues Larissa Rodrigues Souto
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Presidente Prudente, SP, 브라질, 19060-900
- Larissa Rodrigues Souto
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Healthy (self-report);
- Male gender;
- Aged between 18-30 years;
- Agreement to participate through signed statement of informed
Exclusion Criteria:
- Being sick;
- Training or physical activity at least 24 hours priot to the application test;
- Being influenced in some way by test information;
- Do not understand the test;
- Inflammatory process;
- Cardiovascular disease;
- Episode of musculo-tendinous or osteoarticular lesion in the lower limbs and/or spine in the last seix months;
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 다른
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 더블
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
---|---|
실험적: Reliability of IET
In phase 1, the first of familiarization is to the participants understand the test and familiarize with the equipment after 24 to 48 hours, the participants will do the test applied twice at the same day with 10 minutes of rest.
For realization of the IET the participants will be instructe to make the maximum effort as possible and mantain until they can't resiste.
After one week the retest session will be doing.
The order between the evaluators will be changed in the test and retest sessions.
|
The participants will be do three sessions: familiarization, test and retest to assess the reliability inter and intra rater of the test.
|
실험적: Physiological analysis of IET
In phase 2, the participants will be submitted two sessions, familiarization session and test session.
In the test session there is be two teste applied in the same day with approximately 20 minutes of rest.
In the first test, thers is gas analysis during all the test until seven minutes after the test and blood lactat concentrate will be colected before the test with 10 minutes of rest, immediately after the teste and in the first, in the third, fifth and seventh minutes after the test.
In the second test will be assess the muscular activation porcentage of lateral vastus muscle by means of twitch interpolation technique there is be performe before and after the test.
|
The participants will be submitted two sessions, familiarization session and test session.
In the test session there will be the physiological analysis by means of gas analysis, blood lactate concentrate and activation muscular percentage.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
---|---|---|
The time of execution of the test
기간: 45 seconds after the beginning of the test
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This outcome will be assessed in seconds during execution of the test
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45 seconds after the beginning of the test
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
---|---|---|
The work of the test
기간: day 2 and day 7
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This outcome will be assessed in Newton.meter
(N.m) during execution of the test
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day 2 and day 7
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Oxygen consumption - gas analysis
기간: Second phase during all the test
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Gas analysis will be measured during the test and after seven minutes of the same (VO2000, MedGraphics, Minnesota, USA).
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Second phase during all the test
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Blood lactate concentration
기간: Second phase, 10 minutes of rest before the test and immediately after the test and in the third, fifth and seven minutes after the test
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The blood lactate concentration will be collected in the 10 minutes of rest before the test and immediately after the test and in the third, fifth and seven minutes after the test
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Second phase, 10 minutes of rest before the test and immediately after the test and in the third, fifth and seven minutes after the test
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Muscular activation percentage
기간: Day 2
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The muscular activation percentage will be assessed by means of twitch interpolation technique ( current generator - Quark)
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Day 2
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Psychological Questionnaire
기간: Day 2 and day 7
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Participants will be instructed to mark with a dash, on a 10 centimeters analogical visual scale in between two extremes, in which zero means "non-existent" and 10 "very intense" to each classification
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Day 2 and day 7
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Work Ability Index Questionnaire
기간: Day 1
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This questionnaire consists in seven indicators, which provide a score between seven and 49, in which the highest the scores the better.
These indicators evaluate occupational wellness, providing subjective estimation about work capacity, including the ability to perform work tasks in relation to demands, health and mental resources
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Day 1
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Perceived Stress Scale
기간: Day 1
|
This scale is intended to document participants' related stress on the previous month.
Items evaluate the degree to which people find life unpredictable, uncontrollable or overloaded.
This scale evaluates overall beliefs about perceived stress, without the providence of any specific event lists in life to the subjects, allowing these scores not to be biased by the event content or difference of previous life experience
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Day 1
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Bergen Insomnia Scale
기간: Day 1
|
This scale is intended to evaluate participants' sleep and tiredness, which consists in six questions about sleep issues in the previous month.
Questions are about (1) problems initiating sleep, (2) awakening from sleep, (3) early morning awakening, (4) not feeling adequately rested, (5) experiencing daytime impairment and (6) being dissatisfied with sleep.
To each question participants will answer on a zero to seven days a week scale.
The quantity of days will be calculated based on the average of the answers to these six questions, in order to obtain an overall sleep problems score
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Day 1
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Need for Recovery Scale
기간: Day 7
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This is an 11 item scale which aims to evaluate work fatigue symptoms, related to a series of emotional, cognitive and behavioral aspects characterized as temporary overload feelings, irritability, social seclusion, lack of energy for new efforts and performance reduction
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Day 7
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Borg Scale
기간: Day 7
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Participants' physical effort perception will also be measured by the Borg Scale, which will be used to correlate with heart rate values.
After the completion of IET participants willl answer the following question: "How much exertion did you experience during the test?
".
This scale has 15 possible answers, ranging from six to 20, represented respectively from "not exertion at all" to "maximal exertion".
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Day 7
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Borg CR10 Scale
기간: Day 7
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Participants' physical effort perception will be measured by The Borg CR10 Scale.
After the IET application participants will answer the following question: "How much exertion did you experience during the test?
".
This scale has 16 possible answers which vary from zero to 10 represented respectively from no effort to maximum effort.
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Day 7
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Effort Perception Scale
기간: Day 1, day 2 and day 7
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The effort perception will be evaluated by the Effort Perception Scale, with values between 0 and 10, 0 being correspondent to no effort at all (rest) and 10, to maximum effort
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Day 1, day 2 and day 7
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Recovery Perception Scale
기간: Day 1, day 2 and day 7
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The perceived recovery of the dominant lower limb will be assessed by means of the Effort Perception Scale, which consists of a 10-point Likert Scale, in which 1 means no recovery and 10, completely recovered
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Day 1, day 2 and day 7
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Heart Rate
기간: Day 2 and day 7
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The heart rate caption will take place using a cardio frequency meter (Polar electro, Oy Kempele, Finland - V800 model)
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Day 2 and day 7
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공동 작업자 및 조사자
수사관
- 수석 연구원: Carlos Pastre, PhD, Univ Estadual Paulista
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- 2016/11785-7
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
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