NCT07641777

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

75
On Track

Trial Health Score

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

Enrollment
28

participants targeted

Target at below P25 for not_applicable

Timeline
1mo left

Started Feb 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

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 Progress82%
Feb 2026Jul 2026

Study Start

First participant enrolled

February 1, 2026

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

June 6, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

June 11, 2026

Completed
19 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2026

Expected
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

July 15, 2026

Last Updated

June 11, 2026

Status Verified

June 1, 2026

Enrollment Period

5 months

First QC Date

June 6, 2026

Last Update Submit

June 6, 2026

Conditions

Keywords

Coordinated Locomotor TrainingCore StabilityPostural ControlAthletesNeuromuscular Training

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

EXPERIMENTAL

Participants 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).

Other: Coordinated Locomotor TrainingOther: Plyometric Training

Plyometric Training Group

ACTIVE COMPARATOR

Participants 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.

Other: Plyometric Training

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.

Coordinated Locomotor Training Group

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.

Coordinated Locomotor Training GroupPlyometric Training Group

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

Location

MeSH Terms

Interventions

Plyometric Exercise

Intervention Hierarchy (Ancestors)

Exercise TherapyRehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsPhysical Therapy ModalitiesPhysical Conditioning, HumanExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

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

Locations