Neuromuscular Effects of Coordinated Locomotor Training on Core Stability and Postural Control in Athletes
CLT-CORE
1 other identifier
interventional
28
1 country
1
Brief Summary
Core stability and postural control are essential for athletic performance. They affect how efficiently an athlete moves, maintains balance, and avoids injuries. However, researchers have not yet fully explored how coordinated locomotor training - a movement approach that uses walking patterns combined with sprinter and skater positions - changes the way an athlete's nerves and muscles work together. This study aims to compare the effects of coordinated locomotor training versus traditional plyometric exercises on core stability and balance control in novice runners. The study will enroll 28 novice runners between 18 and 30 years of age. Participants must run less than 10 miles per week and have less than one year of consistent running experience. They will be randomly assigned to either the coordinated locomotor training group or the plyometric training group. The intervention lasts 8 weeks with two sessions per week. Each session runs for about 60 minutes. The researchers will measure core endurance using the Mcgill core endurance tests and the Sahrmann core stability test. Dynamic balance will be assessed using the Star Excursion Balance Test. Postural control will be evaluated using the Romberg test. The researchers expect that athletes who undergo coordinated locomotor training will show greater improvements in core muscle activation and postural control compared to those who perform plyometric exercises. If proven effective, this training method could provide coaches and trainers with an evidence-based strategy to enhance athletic performance and reduce injury risk.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2026
CompletedFirst Submitted
Initial submission to the registry
June 6, 2026
CompletedFirst Posted
Study publicly available on registry
June 11, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 15, 2026
June 11, 2026
June 1, 2026
5 months
June 6, 2026
June 6, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Change in Mcgill Core Endurance Test Scores
The Mcgill core endurance tests consist of four subtests: trunk flexor test, trunk extensor test, right side bridge test, and left side bridge test. For each test, participants hold a specific position for as long as possible. The time in seconds is recorded for each position. Longer hold times indicate better core endurance.
Baseline (Week 0) and Week 8 (post-intervention)
Change in Sahrmann Core Stability Test Level
The Sahrmann core stability test consists of 5 progressive levels. Participants start with Level 1 (lifting one leg to 90 degrees hip and knee flexion) and progress through increasing difficulty to Level 5 (lowering both legs simultaneously without heels touching the table). The highest level successfully completed without compensatory movement is recorded. Higher levels indicate better core stability.
Baseline (Week 0) and Week 8 (post-intervention)
Secondary Outcomes (1)
Change in Romberg Test Performance
Baseline (Week 0) and Week 8 (post-intervention)
Study Arms (2)
Coordinated Locomotor Training Group
EXPERIMENTALParticipants in this arm receive coordinated locomotor training (CLT) consisting of sprinter and skater position exercises performed in supine, crawling, sitting, and standing positions. Each session lasts 60 minutes, twice weekly for 8 weeks (16 sessions total).
Plyometric Training Group
ACTIVE COMPARATORParticipants in this arm receive plyometric training consisting of multi-directional jumps and squat jumps onto a 45 cm box. Each session includes warm-up, activation series, and cool-down. Sessions are conducted twice weekly for 8 weeks.
Interventions
Coordinated locomotor training is an exercise technique that visualizes and simplifies human movement by combining walking patterns with sprinter and skater positions. The intervention includes: (1) A 5-minute warm-up familiarizing participants with sprinter and skater techniques in standing position; (2) Main CLT session of 60 minutes performed in supine, crawling, sitting, and standing positions; (3) Each position requires 10 repetitions per set, with 3 sets completed; (4) Total of 16 sessions conducted over 8 weeks, twice per week. The training is supervised by trained physical therapists.
Plyometric training consists of: (1) Warm-up with 2 series of 30 seconds stimulation and 30 seconds cool-down with multi-directional jumps, with 5-second intervals between jumps; (2) 6 series of squat jumps onto a 45 cm box, with 30 seconds activation and 30 seconds relaxation, with 2-second intervals between jumps; (3) Total of 16 sessions conducted over 8 weeks, twice per week. Each session is supervised by trained physical therapists.
Eligibility Criteria
You may qualify if:
- Age between 18 and 30 years
- Running less than 10 miles (approximately 16 kilometers) per week
- Not participating in running sports (such as soccer, track, or cross-country) more than once per week
- Less than one year of consistent running experience
- Male and female novice runners
- Willing to provide written informed consent
You may not qualify if:
- History of musculoskeletal injury (including fractures, ligament tears, or muscle strains) in the past six months
- Diagnosed neurological disorders (such as stroke, multiple sclerosis, or Parkinson's disease)
- Diagnosed vestibular disorders (such as benign paroxysmal positional vertigo or labyrinthitis)
- Presence of current pain, discomfort, or functional limitation during normal daily activities or athletic activities
- Presence of cardiovascular disorders (such as uncontrolled hypertension or heart disease) that restrict moderate to high intensity physical activity
- Presence of respiratory disorders (such as severe asthma or COPD) that restrict moderate to high intensity physical activity
- Regular use of medications that affect neuromuscular performance, coordination, or balance (including sedatives, muscle relaxants, or antiepileptic drugs)
- Pregnancy
- Any condition that, in the opinion of the investigator, would preclude safe participation in exercise training
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The University of Faisalabad
Faisalābad, Punjab Province, 3800, Pakistan
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Masking Details
- The outcome assessors and data analysts will be blinded to group allocation. Participants and intervention providers cannot be blinded due to the nature of the exercise interventions.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor, Department of Rehabilitation Sciences
Study Record Dates
First Submitted
June 6, 2026
First Posted
June 11, 2026
Study Start
February 1, 2026
Primary Completion (Estimated)
June 30, 2026
Study Completion (Estimated)
July 15, 2026
Last Updated
June 11, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will not share