Skip to content

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

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07716319
Enrollment
90
Registered
2026-07-21
Start date
2026-09-01
Completion date
2027-09-01
Last updated
2026-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Keywords

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

Brief 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.

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.

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.

Sponsors

University of Wisconsin, Madison
Lead SponsorOTHER
National Strength and Conditioning Association (NSCA) Foundation
CollaboratorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 25 Years
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

* 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

Design outcomes

Primary

MeasureTime frame
Change in fascicle length (FL)Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
Change in muscle cross-sectional area (CSA)Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
Change in muscle volumeBaseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
Change in pennation angle (PA)Baseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)

Secondary

MeasureTime frameDescription
Change in eccentric strengthBaseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)Eccentric hamstring strength of each limb will be assessed during the hamstring exercise.
Change in inertial measurement units (IMU)-based sprinting biomechanicsBaseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)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.
Change in countermovement jump (CMJ) performanceBaseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
Change in standing broad jump (SBJ) performanceBaseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
Change in change of direction (CoD) performanceBaseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
Change in range of motion (ROM) performanceBaseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
Change in hip flexionBaseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)
Change in anterior pelvic tiltBaseline to Mid-intervention (6 weeks), Post-intervention (10 weeks), and Post 2 week de-training (12 weeks)

Countries

United States

Contacts

CONTACTScott K Crawford, PhD
skcrawford2@wisc.edu608) 265-1308

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 22, 2026