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Life Kinetic Training Enhances Physical and Cognitive Skills in Young Fencers

Impact of Life Kinetic Training on Balance, Agility, Jumping, Proprioception, and Cognitive Function in Preadolescent Recreational Fencing Athletes: a Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06781268
Acronym
LiKT-Fence RCT
Enrollment
22
Registered
2025-01-17
Start date
2024-02-27
Completion date
2024-09-15
Last updated
2025-01-17

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

Conditions

Healthy

Keywords

Children, Life kinetic, Motor skills, Exercise, Physical fitness

Brief summary

The purpose of this study was to examine whether Life Kinetic (LK) exercises could improve balance, agility, jumping performance, proprioception, and cognitive functions in recreationally active preadolescents participating in fencing. It specifically aimed to answer if LK training would lead to significant enhancements in these physical and cognitive attributes compared to a control group.

Detailed description

This study evaluated the effects of Life Kinetic (LK) training on balance, agility, jumping performance, proprioception, and cognitive functions in preadolescent recreational fencers. A total of 22 participants, aged 11.6 ± 1.2 years, were randomly assigned to either the experimental group, which performed LK exercises twice weekly for eight weeks, or the control group, which continued their regular fencing activities. The LK exercises combined physical and cognitive tasks to stimulate neuroplasticity and improve overall athletic and mental performance. Key metrics included agility, vertical jump, star balance, Stroop test, and proprioception assessments.

Interventions

BEHAVIORALLife Kinetic Training

Combination of cognitive and physical exercises aimed at improving neuroplasticity, agility, balance, and cognitive functions.

Sponsors

Democritus University of Thrace
CollaboratorOTHER
Hellenic Naval Academy
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
10 Years to 12 Years
Healthy volunteers
Yes

Inclusion criteria

* Preadolescents aged between 10 and 12 years. Recreationally active in fencing and registered with the same athletic club. Healthy participants with no chronic illnesses, musculoskeletal injuries, or physical limitations in the last six months. No use of medication within six months prior to the study. Written informed consent provided by the participants and their parents or guardians.

Exclusion criteria

* History of chronic illnesses or conditions that could interfere with physical activity (e.g., asthma, cardiovascular issues). Any injury or physical limitation in the last six months that could impact performance. Use of medication that could affect physical or cognitive performance within six months before the study. Participants outside the specified age range (10-12 years). Lack of parental or participant consent.

Design outcomes

Primary

MeasureTime frameDescription
Y Balance Test8 weeksBefore screening, participants removed their socks and shoes, watched a brief instructional video on performing the Y Balance Test (YBT), and were allowed 4 to 6 practice trials for each limb in each of the three reach directions. Following the practice trials, we measured the lower extremity length from the inferior border of the anterior superior iliac spine to the inferior border of the medial malleolus. Participants then performed dynamic balance tests on both the right and left lower extremities, reaching in the anterior (ANT), posteromedial (PM), and posterolateral (PL) directions with the contralateral limb. Three successful reaches were recorded, and the maximal reach distance in each direction was used for data analysis. To obtain relative values for each direction for both the right and left limbs, the following formula was applied: Relative (normalized) reach distance (%) = (Absolute reach distance / Limb length) × 100.
Stroop Color and Word Test8 weeksA Stroop test comprising three distinct conditions was employed (Scarpina and Tagini, 2017). Each condition featured 60 stimuli, arranged with 6 items per line on a 21.5 × 29 cm sheet of paper. In the initial condition, referred to as the reading condition, participants were required to read words printed in black ink, which included the names of colors such as red, green, blue, and yellow. In the second condition, known as the naming condition, participants were instructed to identify the colors of various rectangles. In the third condition, termed the interference condition, participants were required to name the color of the ink used to print the words, while disregarding the semantic content of the words themselves, as they were incongruent with the ink color (e.g., the word green printed in red ink). This condition specifically tested the participants' inhibitory control. Across all conditions, participants were instructed to respond as quickly as possible while minimizing erro
Agility T-test8 weeksThe T-test was conducted as previously described (Semenick, 1990). Four cones were positioned in a T formation, with one cone located 9.14 meters from the starting cone and two additional cones placed 4.57 meters on either side of the second cone. All times were recorded using an electronic timing gate (Fusion Sport Inc.), set at a height of 0.75 meters and spanning 3 meters wide, aligned with the marked starting point. Participants were instructed to sprint forward 9.14 meters from the starting line to the first cone, touching it with their right hand. They then shuffled 4.57 meters to the left to reach the second cone, touching it with their left hand. Subsequently, they shuffled 9.14 meters to the right to the third cone, touching it with their right hand, and shuffled 4.57 meters back to the middle cone, touching it with their left hand. Finally, they backpedaled to the starting line. Timing commenced as participants passed through the timing gates and concluded upon their return
Proprioception Test8 weeksFor the position perception test, the IsoMed-2000 isokinetic testing apparatus was utilized (IsoMed-2000 dynamometer; D & R Ferstl GmbH, Hemau, Germany) as described by Wang et al. (2023). Participants wore headphones and an eye mask to eliminate external auditory and visual influences. They maintained their knee joint in the testing position, allowing the isokinetic device (operating at an angular velocity of 1°/s) to automatically flex and extend to the predetermined angles of 30° and 60°.When the angle returned to 0°, the participant moved to the specified position after the automatic stop of the button movement. The difference between the actual angle and the pre-set angle was recorded. Each angle test was conducted three times to calculate the average value.
Counter Movement Jump Measurement8 weeksThe counter movement jump (CMJ) was assessed utilizing the OptoJump Next system (Microgate, Bolzano, Italy). After a self-administered warm-up session, participants performed 3 trials of the counter-movement jump without arm swings, followed by a one-minute rest period, after which they completed the actual CMJ test. Each participant completed three repetitions of the CMJ without arm swings, and the highest result in centimeters (jumping height) was documented as the primary outcome measure. The OptoJump, a dual-beam optical apparatus, quantifies contact and flight durations during jump sequences (or individual jumps). Flight time (tair) was employed to determine the elevation of the body's center of gravity.

Secondary

MeasureTime frameDescription
Body height8 weeksBody height was measured with participants standing upright, feet together, back against the wall, and recorded to the nearest 0.1 cm as the maximum distance from the floor to the highest point on the head.
Leg length8 weeksLeg length was measured using a tape measure from the anterior superior iliac spine (ASIS) to the medial malleolus. Leg length measurements were taken three times for each limb with the participants in a lying position (Sabharwal and Kumar, 2008).
Body weight8 weeksBody weight was measured with participants wearing light underwear, standing, and with a precision of 0.1 kg.

Countries

Greece

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026