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Not yet recruitingNCT07716319Updated Jul 21, 2026

Comparison Between Eccentric Hamstring Training and Sprint-Specific Training

An interventional study of RDL and NHE in Healthy Adult, Athlete and Exercise Training, sponsored by University of Wisconsin, Madison. Not yet recruiting at 1 site in United States. Open to participants aged 18 Years to 25 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-21.

Sponsored by University of Wisconsin, Madison · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
90
Allocation
Randomized
Ages
18 Years to 25 Years
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Healthy Adult
  • Athlete
  • Exercise Training
  • Sport
  • Running
  • Ultrasound Imaging

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Keywords

  • strength
  • agility
  • sprint
  • hypertrophy
  • countermovement jump
  • fascicle length
  • hamstring
  • range of motion
03

Who can participate

Ages eligible
18 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

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

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
04

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
90 participants (estimated)

Study arms

  • Experimental
    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.

    Other: RDL

  • Experimental
    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

    Other: NHE

  • Experimental
    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.

    Other: Sprint testing

Interventions

  • OtherRDL

    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.

  • OtherNHE

    The NHE will be performed with a 6 second eccentric component.

  • OtherSprint testing

    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.

05

What researchers measure

Primary outcomes

  1. Change in fascicle length (FL)

    Time frame: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)

  2. Change in muscle cross-sectional area (CSA)

    Time frame: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)

  3. Change in muscle volume

    Time frame: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)

  4. Change in pennation angle (PA)

    Time frame: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)

Secondary outcomes

  1. Change in eccentric strength

    Eccentric hamstring strength of each limb will be assessed during the hamstring exercise.

    Time frame: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)

  2. Change in inertial measurement units (IMU)-based sprinting biomechanics

    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.

    Time frame: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)

  3. Change in countermovement jump (CMJ) performance

    Time frame: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)

  4. Change in standing broad jump (SBJ) performance

    Time frame: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)

  5. Change in change of direction (CoD) performance

    Time frame: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)

  6. Change in range of motion (ROM) performance

    Time frame: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)

  7. Change in hip flexion

    Time frame: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)

  8. Change in anterior pelvic tilt

    Time frame: Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)

06

Study locations

1 site
  • University of Wisconsin - Madison
    Madison, Wisconsin 53705, United States
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07716319
Lead sponsor
University of Wisconsin, Madison
Collaborators
National Strength and Conditioning Association (NSCA) Foundation
Responsible party
Sponsor
First posted
Jul 21, 2026
Start date
Sep 2026 (estimated)
Primary completion
Sep 2027 (estimated)
Completion
Sep 2027 (estimated)
Last update
Jul 21, 2026

Study contacts

Scott K Crawford, PhD
Contact
skcrawford2@wisc.edu
608) 265-1308

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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