- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07716319
Comparison Between Eccentric Hamstring Training and Sprint-Specific Training
Comparison Between Eccentric Hamstring Strength Training and Sprint-Specific Training on Muscle Hypertrophy, Strength, Power, and Sprint Performance in Club Sport Collegiate Athletes
The purpose of this study is to compare the effects of an intensity-, volume-, and time under tension-matched eccentric hamstring exercise intervention with the Romanian deadlift (RDL) and the Nordic hamstring exercise (NHE) to a sprint-specific training program on hamstring muscle architecture, volume, sprint performance, strength, and power.
Participants will be assigned to complete one of the 3 hamstring interventions for 10 weeks.
연구 개요
상세 설명
Prior to the intervention, participants will undergo baseline testing which will include a) ultrasound imaging of the hamstrings muscles for measures of biceps femoris long head fascicle length, pennation angle, muscle thickness, anatomical cross-sectional area, and muscle volume b) passive and active ranges of motion, c) 3 repetition maximum (3RM) RDL strength, d) peak NHE force, e) countermovement jump height, f) broad jump distance, g) Pro Agility change of direction, and h) a 60 m sprint with sprint kinematics assessed via inertial measurement units.
Participants will be randomly assigned to either the RDL, NHE, or sprint training group. After randomization, each participant will undergo the intervention program based upon their group allocation.
Performance testing and imaging will be repeated mid-intervention, following the intervention, and after 2 weeks of deloading.
연구 유형
등록 (추정된)
단계
- 해당 없음
연락처 및 위치
연구 연락처
- 이름: Scott K Crawford, PhD
- 전화번호: 608) 265-1308
- 이메일: skcrawford2@wisc.edu
연구 장소
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Wisconsin
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Madison, Wisconsin, 미국, 53705
- University of Wisconsin - Madison
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연락하다:
- Scott K Crawford, PhD
- 전화번호: 608-265-1308
- 이메일: skcrawford2@wisc.edu
-
-
참여기준
자격 기준
공부할 수 있는 나이
- 성인
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
- Age 18-25 years
- Actively participating in a club team
- >6 months experience with resistance training
- Minimum of 1 year experience at the high school level in organized team sport
- No history of hamstring injury within the last 6 months
- No history of major lower extremity surgery (including back)
- No acute musculoskeletal injury to the lower extremity
- Not currently pregnant
Exclusion Criteria:
- Unable to refrain from resistance training outside the study
- Unable to make at least 80% of the training sessions
- Hamstring injury in the last 6 months
- History of major lower extremity surgery (including back)
- Acute musculoskeletal injury to the lower extremity
- Currently pregnant
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 |
|---|---|
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실험적: Romanian dead lift (RDL) group
The training intervention groups will undergo the same program with the only difference being the interventional hamstring exercise.
The program will consist of a 2-week familiarization period followed by 8 weeks of progressive training.
The RDL arm will perform RDL.
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The RDL will be performed with a 6 second eccentric component with the athlete returning to the start position with a maximal concentric hip extension.
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실험적: Nordic hamstring exercise (NHE) group
The training intervention groups will undergo the same program with the only difference being the interventional hamstring exercise.
The program will consist of a 2-week familiarization period followed by 8 weeks of progressive training.
The NHE arm will performed NHE
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The NHE will be performed with a 6 second eccentric component.
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실험적: Sprint group
The training intervention groups will undergo the same program with the only difference being the interventional hamstring exercise.
The program will consist of a 2-week familiarization period followed by 8 weeks of progressive training.
The sprint training program will be performed twice per week with the first day of training focused on shorter distances to focus on acceleration and the second training day focused on maximal velocity.
The relative efforts and distances for each training day will mimic a similar prescription to that of the resistance training program.
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The sprint training program will be performed twice per week with the first day of training focused on shorter distances to focus on acceleration and the second training day focused on maximal velocity.
The relative efforts and distances for each training day will mimic a similar prescription to that of the resistance training program.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
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Change in fascicle length (FL)
기간: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Change in muscle cross-sectional area (CSA)
기간: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Change in muscle volume
기간: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Change in pennation angle (PA)
기간: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Change in eccentric strength
기간: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Eccentric hamstring strength of each limb will be assessed during the hamstring exercise.
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Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Change in inertial measurement units (IMU)-based sprinting biomechanics
기간: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Sprinting biomechanics will be assessed using seven IMUs (sacrum, both thighs, both shanks, both feet).
Lower extremity joint motions referenced to upright stance will be calculated throughout an on-field sprint and other football drills.
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Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Change in countermovement jump (CMJ) performance
기간: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Change in standing broad jump (SBJ) performance
기간: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Change in change of direction (CoD) performance
기간: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Change in range of motion (ROM) performance
기간: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Change in hip flexion
기간: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Change in anterior pelvic tilt
기간: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
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공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
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
- 2026-0704
- UWMSN | SOE | Kinesiology Oper (기타 식별자: UW- Madison)
- Protocol Version 5/5/26 (기타 식별자: UW- Madison)
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
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RDL에 대한 임상 시험
-
Riverside Pharmacueticals Corporation완전한
-
University of Wisconsin, Madison완전한