Skip to content

Evaluation of biomechanical sprinting parameters following the application of Lightback® in elite sprinters.

The Effects of Lightback® on Ground Contact Length in elite Sprinters.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12626001081303
Enrollment
12
Registered
2026-09-02
Start date
2026-10-01
Completion date
2026-11-01
Last updated
2026-09-07

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

Conditions

None listed

Brief summary

To determine the effectiveness of hip compression using the LightBack® device on sprinting kinematics and range of motion in elite sprinters following sprints. We hypothesize that LightBack mobilization significantly increases hip range of motion and optimizes sprinting performance (kinematics) post-exertion.

Interventions

1. Conditioning and Baseline Phase Participants perform a standardized specific warm-up under the direct supervision of a qualified CAR sports scientist and sprint/strength coach, lasting between 35 to 50 minutes, which includes 5 minutes of low-intensity jogging, dynamic stretches for the upper and lower limbs, sprint drills (e.g., high knee runs, skips, and bounds), and 3 progressive sprints building up to 95% of maximum effort. This is followed by a series of resisted sprints with incremental

1. Conditioning and Baseline Phase Participants perform a standardized specific warm-up under the direct supervision of a qualified CAR sports scientist and sprint/strength coach, lasting between 35 to 50 minutes, which includes 5 minutes of low-intensity jogging, dynamic stretches for the upper and lower limbs, sprint drills (e.g., high knee runs, skips, and bounds), and 3 progressive sprints building up to 95% of maximum effort. This is followed by a series of resisted sprints with incremental loads using the DynaSpeed system (towing/resisted cable device) ranging from overspeed/assistance conditions (5% top-speed increase or 5 kg pulling force) to resisted loads inducing 10%, 25%, 50%, and 65% velocity loss. These sprints range from 40 to 100 meters in distance, with recovery intervals adjusted accordingly based on the specific sprint distance and the load applied by the DynaSpeed device, calculated as a minimum of 3 to 5 minutes of passive rest for shorter distances (20–30 m) and at least 5 minutes of passive recovery between repetitions for longer or heavier sprints to ensure non-fatigued states. Following this conditioning phase, a maximal effort sprint is performed to record baseline biomechanical data (Pre-intervention). Immediately following the baseline sprint, the Lightback® intervention is applied bilaterally (on both legs) in a one-on-one session directly supervised by the Principal Investigator (PI), who is a qualified physiotherapist, at the High Performance Center (Centro de Alto Rendimiento - CAR) of Madrid. This intervention uses the Lightback® device, a passive joint compression apparatus designed to perform a self-passive anterior-posterior (A-P) mobilization of the femur to induce controlled posterior femoral gliding, reduce deep gluteal muscle tension, and optimize hip joint mobility through a stretch of the posterior hip capsule and gluteal muscles. Procedure per leg: The athlete is seated on the Lightback® device, bringing the knee toward the chest until reaching 90º of hip flexion. Dosage: Once the subject reaches the maximum sensation of stretching without pain, the position is held for 10 seconds, followed by a 5-second relaxation period. This sequence is repeated 6 times for a total application time of one minute per leg. 3. Post-Intervention Assessment: 10 minutes after the Lightback® application, participants perform a second maximal effort sprint (Post-intervention). Biomechanical parameters are recorded using the same methodology as the baseline test to determine the acute effects of the intervention on sprinting performance and technique.

Sponsors

Universidad Europea de Madrid
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Intervention model
Other
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

Elite sprinters affiliated with the High Performance Center (CAR) in Madrid. Competitive experience at the national or international level in sprint events (60m, 100m, 200m, or 400m). Maintaining a high-performance training regimen of at least five sessions per week.

Exclusion criteria

Exclusion criteria were individuals with a history of musculoskeletal lower limb or lumbopelvic conditions within the last five years, as well as those with neuromuscular, rheumatic, cardiovascular or neurological diseases, and those who had undergone previous surgical interventions or experienced fractures in the lower extremities or abdominal region. - To be pregnant - Allergic to a material in the machine (polyurethane foam, synthetic leather/vinyl upholstery) - To experience any type of pain during the procedure

Outcome results

None listed

Source: ANZCTR · Data processed: Sep 19, 2026