Skip to main content
OpenTrials
Completed

NCT Number: NCT05455346

Eccentric Training Effects on Hamstrings Structure, Strength, and Sprint Performance

The overall goal of this study is to investigate the effects of a 6-week training program between two hamstring exercises-the Romanian deadlift (RDL) and the Nordic hamstring exercise (NHE)-on hamstring strain injury risk factors and sprint performance.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–25 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Wisconsin

Madison, Wisconsin, 53705, United States

About this study

Prior to the intervention, participants will report to the lab on one occasion for baseline assessments. During the baseline visit, a) regional measures of biceps femoris long head fascicle length, pennation angle, muscle thickness, and anatomical cross-sectional area will be determined using ultrasound, b) baseline NHE strength and 3RM for the RDL will be determined, and c) maximal 60 m sprint performance will be measured.

Participants will be randomly assigned to either the RDL or NHE. After randomization, each participant will undergo the 6 week intervention program based upon their group allocation. Exercises will be performed using a 6 second eccentric (i.e., lowering) contraction.

Following the 6 week intervention, participants would return to the lab for post-intervention assessments of regional hamstring morphology and architecture and sprint testing, which would be carried out in the same manner as baseline assessments. Since fascicle length changes are known to return to baseline values within 2 weeks after the cessation of eccentric training, participants will be asked to return to the lab following a 2 week detraining period where final imaging, strength, and sprint performance assessments will be determined.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18-25 years of age
  • Have >6 months experience in resistance training

Exclusion criteria

  • History of hamstring strain injury within the last 12 months
  • History of lower extremity surgery
  • Current musculoskeletal injury to the lower extremity
  • Females who are currently pregnant
  • Individuals who indicate they are unwilling to refrain from novel outside training activities
  • Individuals who do not complete 75% (9 out of 12) of the training sessions

Treatment and study plan

Ultrasound imaging

Diagnostic Test

Ultrasound B-mode images will be unilaterally collected from the biceps femoris muscle of the dominant limb for each participant using a commercial ultrasound system and linear array transducer. Standardized image locations will correspond to 33%, 50%, and 67% of the thigh length from the ischial tuberosity.

Three repeat longitudinal extended-field-of-view images of the entire biceps femoris muscle will be collected for offline analysis for fascicle length, muscle thickness, and pennation angle. Transverse extended-field-of-view images will be captured at the proximal, mid-belly, and distal locations to determine regional anatomical cross-sectional area of the biceps femoris long head muscle.

To determine changes in tissue stiffness via ultrasound shear wave speed, the same transducer will be placed in the same locations in a longitudinal view. Shear wave maps will be generated by the ultrasound system and shear wave speed measures extracted from the middle of the map.

Hamstring Eccentric Strength Testing

Other

Prior to each test, participants will perform a standardized 5-minute general warm-up followed by a task-specific warm-up including 3 sets of submaximal trials. Load increases (5-20%) will be added for each RDL 3-repetition maximum trial attempt until the participant cannot complete 3 repetitions through the full range of motion using proper technique. A 3-minute rest will be administered between all warm-up and testing sets to allow for full recovery.

Participants will kneel on a commercial device used to assess maximum eccentric knee flexor strength via uniaxial load cells with their ankles secured into fixed hooks. Participants will slowly lower their torso to the ground with arms crossed across their chest and without bending at the hips or spine. The maximal test will consist of 1 set of 3 maximal repetitions. If participants can control lower themselves to the ground, then they will hold barbell plates (5-10 lb increments) across their chest while performing the NHE.

Maximal 60 m Sprint

Other

Following a standardized warm-up, inertial measurement units (IMUs) will be placed on the sternum, sacrum, and bilaterally on the thighs, legs, and foot. Each participant will perform a total of 3 maximal 60 m sprints from a standing position with 1.5-3 min rest in between each trial to minimize the effects of fatigue.

Romanian Deadlift

Other

The RDL intervention will be performed twice per week for 6 weeks. Participants will hinge at the hips lowering the bar to just below their patella before reversing the movement. The RDL will be performed with a 6 second eccentric component and returning to the start position with a maximal concentric hip extension.

Other names: RDL

Nordic Hamstring Exercise

Other

The NHE will be performed twice per week for 6 weeks. Participants will be instructed to maintain their ankles in a dorsiflexed position, lower themselves as close to the ground as possible at a constant and controlled speed while maintaining a neutral position of the hips and trunk, and to cross their arms in front of their chest.

Other names: NHE

Primary outcomes

  1. Biceps femoris long head fascicle length

    Time frame: Baseline

  2. Biceps femoris long head fascicle length

    Time frame: Post-intervention (6 weeks)

  3. Biceps femoris long head fascicle length

    Time frame: Post 2 week de-training (8 weeks)

Secondary outcomes

  1. Biceps femoris long head pennation angle

    Time frame: Baseline, Post-intervention (6 weeks), Post 2 week de-training (8 weeks)

  2. Biceps femoris long head muscle thickness

    Time frame: Baseline, Post-intervention (6 weeks), Post 2 week de-training (8 weeks)

  3. Biceps femoris long head anatomical cross sectional area

    Time frame: Baseline, Post-intervention (6 weeks), Post 2 week de-training (8 weeks)

  4. Romanian deadlift (RDL) 3-repetition maximal strength

    Time frame: Baseline, Post-intervention (6 weeks), Post 2 week de-training (8 weeks)

    Maximum weight lifted for 3 repetitions during the RDL

  5. Nordic hamstring exercise (NHE) maximal strength

    Time frame: Baseline, Post-intervention (6 weeks), Post 2 week de-training (8 weeks)

    Maximal eccentric force measured by Nordbord device during NHE

  6. Maximal 60 m sprint times

    Time frame: Baseline, Post-intervention (6 weeks), Post 2 week de-training (8 weeks)

    Fastest 60 m sprint times with interval split times

Other outcomes

  1. Biceps femoris long head regional shear wave speed

    Time frame: Baseline, Post-intervention (6 weeks), Post 2 week de-training (8 weeks)

  2. Inertial measurement unit (IMU)-derived trunk, hip, knee, and ankle kinematics

    Time frame: Baseline, Post-intervention (6 weeks), Post 2 week de-training (8 weeks)

Sponsors and collaborators

Lead sponsor

University of Wisconsin, Madison

Other

Registry information

Official study title

Changes in Biceps Femoris Architecture, Hamstrings Eccentric Strength, and Sprint Performance Following Romanian Deadlift vs. Nordic Hamstring Exercise Intervention

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Jul 13, 2022
Registry last updated
Dec 21, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.