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Not yet recruiting NCT07648537

The Effect of Muscular Fatigue on Lower Limb Kinematics During Single-Leg Drop Landing in Female Athletes

No phase Interventional Athletes

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: fatigue protocol.
Who it may be relevant to
Registry conditions: Athletes. Basic parameters: 20 years — 25 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

this study will be conducted to investigate the effect of muscular fatigue on lower limb kinematics during single-leg drop landing in female professional volleyball players using a mobile-based motion analysis application.

Detailed description

Muscular fatigue impairs neuromuscular control and alters lower limb kinematics during dynamic tasks such as landing, increasing the risk of injury. For example, repetitive jump-landing tasks, as frequently performed in volleyball, have been shown to induce progressive changes in lower limb biomechanics, including reduced ankle plantarflexion and altered knee alignment, which may compromise energy absorption and joint stability.Female athletes face a higher incidence of knee and ligament injuries than males, including ACL tears and ankle sprains, due to sex-specific biomechanical and neuromuscular characteristics such as reduced hamstring activation, increased joint laxity, and altered landing mechanics .Markerless, smartphone-based systems such as OpenCap provide a validated, cost-effective, and field-based solution for 3D kinematic analysis.By applying OpenCap to evaluate the effects of muscular fatigue on single-leg drop landing in professional female volleyball players, this study aims to detect early deviations in movement patterns that may predispose athletes to injury. These findings can inform preseason screening and guide the development of tailored neuromuscular training programs, contributing to context-specific, sex-informed injury prevention strategies in female sport

Interventions

  • Other fatigue protocol
    Before formal testing, participants will perform a five-minute warm-up replicating their usual pre-volleyball training routine. Following the warm-up, the single-leg drop landing (SLDL) task will be clearly explained and demonstrated to all participants.Stand barefoot on both legs on a 30 cm box, then extend the testing leg forward. They will then step off the box using the testing leg, land on the same leg with a toe-heel landing pattern. After familiarization, participants will perform three t

Primary outcome measures

  • hip range of motion [Time frame: up to one day]
  • knee flexion range of motion [Time frame: up to one day]
  • ankle dorsiflexion range of motion [Time frame: up to one day]
  • knee valgus angle [Time frame: up to one day]

Eligibility criteria

Inclusion criteria

  • Female volleyball players aged 20-25 years
  • Practice professional volleyball training or competition experience of at least 2 years
  • typically engage in a high volume of training, with regular participation in at least five training sessions per week
  • Willingness to adhere to fatigue protocol and provide informed consent

Exclusion criteria

  • Current or recent (within the past 6 months) lower limb injury or medical condition
  • History of lower limb surgeries
  • Neurological disorders or balance impairments .
  • Experiencing pain or discomfort during jumping or landing tasks
  • Body mass index (BMI) greater than 30 kg/m²
  • Inability to comply with the fatigue protocol or follow instructions for the landing tasks

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Diagnostic

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07648537 · P.T.REC/012/0067282

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗