NCT06781268

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
22

participants targeted

Target at P25-P50 for not_applicable healthy

Timeline
Completed

Started Feb 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 27, 2024

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 12, 2024

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 15, 2024

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

January 4, 2025

Completed
13 days until next milestone

First Posted

Study publicly available on registry

January 17, 2025

Completed
Last Updated

January 17, 2025

Status Verified

January 1, 2025

Enrollment Period

3 months

First QC Date

January 4, 2025

Last Update Submit

January 15, 2025

Conditions

Keywords

ChildrenLife kineticMotor skillsExercisePhysical fitness

Outcome Measures

Primary Outcomes (5)

  • Counter Movement Jump Measurement

    The 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.

    8 weeks

  • Stroop Color and Word Test

    A 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

    8 weeks

  • Agility T-test

    The 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

    8 weeks

  • Proprioception Test

    For 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.

    8 weeks

  • Y Balance Test

    Before 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.

    8 weeks

Secondary Outcomes (3)

  • Body weight

    8 weeks

  • Body height

    8 weeks

  • Leg length

    8 weeks

Study Arms (2)

Life Kinetic Training Group

EXPERIMENTAL

Participants in this group engaged in Life Kinetic (LK) exercises twice a week for eight weeks. The training program combined physical and cognitive tasks designed to enhance neuroplasticity, improve balance, agility, jumping performance, proprioception, and cognitive functions. The exercises included activities that stimulated mental and physical coordination, aimed at improving overall athletic and mental performance.

Behavioral: Life Kinetic Training

Control group

NO INTERVENTION

Participants in the control group continued their usual recreational fencing training without additional intervention. To match the exposure of the experimental group, they engaged in structured, low-intensity activities unrelated to the objectives of Life Kinetic Training. These activities included light stretching, basic coordination drills, and non-cognitive motor tasks, conducted at the same frequency and duration as the experimental sessions (twice per week for one hour). These activities were designed to simulate a training environment while lacking the cognitive and motor integration components central to the intervention. At the end of the study, participants were fully debriefed about the nature and purpose of their activities, including the rationale for the placebo-like design, as part of the ethical protocol.

Interventions

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

Life Kinetic Training Group

Eligibility Criteria

Age10 Years - 12 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hellenic Naval Academy

Athens, Greece

Location

Related Publications (1)

  • Yarayan YE, Keskin K, Celik OB, Guder BC, Kurtipek S, Aslan M, Sogut T, Durhan TA, Alkhamees NH, Sheeha BB, Alghannam AF, Al-Mhanna SB, Grivas GV, Batrakoulis A. Impact of life kinetik training on balance, agility, jumping, proprioception, and cognitive function in preadolescent recreational fencing athletes: a randomized controlled trial. BMC Sports Sci Med Rehabil. 2025 Jun 7;17(1):146. doi: 10.1186/s13102-025-01186-3.

MeSH Terms

Conditions

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

January 4, 2025

First Posted

January 17, 2025

Study Start

February 27, 2024

Primary Completion

May 12, 2024

Study Completion

September 15, 2024

Last Updated

January 17, 2025

Record last verified: 2025-01

Data Sharing

IPD Sharing
Will not share

IPD will not be shared to ensure the privacy and confidentiality of participants. Additionally, explicit consent for data sharing was not obtained from participants or their guardians during the study, and the ethical approval did not include provisions for sharing individual data externally.

Locations