HVLA Talocrural Distraction Technique Effects on Soccer Players' Ankle Mobility and Pressure Distribution
high-speed, low-amplitude talocrural decompression technique and changes at the level of mobility and plantar pressure
+ simulated ankle technique
Leg Injuries
+ Wounds and Injuries
+ Ankle Injuries
Treatment Study
Summary
Study start date: December 1, 2024
Actual date on which the first participant was enrolled.This study aims to examine the immediate effects of a specific physiotherapy technique on ankle movement and foot pressure patterns in amateur soccer players. The technique being studied is a high-velocity, low-amplitude (HVLA) method applied to the ankle joint to see if it improves how the foot moves and distributes weight during activities, which is crucial for soccer players. Understanding these effects could help in developing better treatment methods for athletes to enhance their performance and potentially reduce the risk of injury. Participants in this trial are divided into two groups. One group receives the actual HVLA treatment, where the technique is performed on their ankle, while the other group experiences a simulated version that does not include the actual technique. The study measures changes in ankle movement and foot pressure distribution after the treatment to assess its effectiveness. By comparing the results between the real and simulated groups, researchers hope to determine if this technique can provide measurable benefits in terms of mobility and pressure distribution in soccer players.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.40 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Male
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy Objectives
Primary Objectives