NCT07596420

Brief Summary

This randomized controlled trial aims to investigate the effects of an 8-week structured neuromuscular exercise program on running performance and lower extremity biomechanics in recreational runners. The program includes progressive exercises focusing on hip and core strength, balance, plyometric control, and running-specific mobility. Participants will be randomly assigned to an intervention or control group. The intervention group will perform the neuromuscular training twice a week for eight weeks, while the control group will not receive any structured exercise. Pre- and post-intervention assessments will include biomechanical analysis and functional performance tests. The study aims to provide evidence for the preventive and performance-enhancing benefits of neuromuscular training in runners.

Trial Health

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Trial Health Score

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

Enrollment
24

participants targeted

Target at below P25 for not_applicable

Timeline
3mo left

Started May 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet 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 Progress18%
May 2026Sep 2026

First Submitted

Initial submission to the registry

January 1, 2026

Completed
4 months until next milestone

Study Start

First participant enrolled

May 1, 2026

Completed
18 days until next milestone

First Posted

Study publicly available on registry

May 19, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2026

Last Updated

May 19, 2026

Status Verified

January 1, 2026

Enrollment Period

4 months

First QC Date

January 1, 2026

Last Update Submit

May 12, 2026

Conditions

Keywords

Neuromuscular ExercisePerformance, BalanceCore StrengthHip StabilityLower Limb BiomechanicsInjury PreventionRunning Training

Outcome Measures

Primary Outcomes (1)

  • Running performance

    Change in running performance will be assessed using a standardized time-trial test to evaluate the effectiveness of the neuromuscular exercise program in improving endurance and speed in recreational runners.

    Baseline and after 8 weeks of intervention

Secondary Outcomes (2)

  • Dynamic balance

    Baseline and after 8 weeks of intervention

  • Lower limb strength

    Baseline and after 8 weeks of intervention

Study Arms (2)

NEUROMUSCULAR EXERCISE GROUP

EXPERIMENTAL

Participants in this group will not receive any structured exercise program during the 8-week intervention period. They will maintain their usual physical activity and running habits. Assessments will be performed at the same pre- and post-intervention time points as the intervention group.

Behavioral: Structured Neuromuscular Exercise Program

CONTROL GROUP

NO INTERVENTION

Participants in this group will not receive any structured exercise program during the 8-week intervention period. They will maintain their usual physical activity and running habits. Assessments will be performed at the same pre- and post-intervention time points as the intervention group.

Interventions

An 8-week structured neuromuscular exercise program including progressive exercises targeting hip and core strength, dynamic balance, plyometric control, and running-specific mobility. The program is performed twice per week under supervision. It is designed to improve running performance, neuromuscular control, and lower limb biomechanics in recreational runners.

NEUROMUSCULAR EXERCISE GROUP

Eligibility Criteria

Age18 Years - 55 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Age between 18 and 55 years
  • Recreational runners who have been running regularly (at least twice per week for the last 6 months)
  • No current musculoskeletal injury limiting running
  • Willing to participate in the 8-week neuromuscular exercise program and attend follow-up assessments
  • Able to provide informed consent

You may not qualify if:

  • History of lower limb surgery or fracture in the past 6 months
  • Neurological, vestibular, or systemic diseases affecting balance or gait
  • Current participation in a structured strength or neuromuscular training program
  • Pregnancy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Pt Academy

Kadıköy, Istanbul, 34726, Turkey (Türkiye)

Location

Related Publications (1)

  • Hammes D, Aus der Funten K, Kaiser S, Frisen E, Bizzini M, Meyer T. Injury prevention in male veteran football players - a randomised controlled trial using "FIFA 11+". J Sports Sci. 2015;33(9):873-81. doi: 10.1080/02640414.2014.975736. Epub 2014 Nov 5.

    PMID: 25370591BACKGROUND

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
This is an open-label study; no masking is applied. Both participants and investigators are aware of the group assignments.
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: Participants will be randomly assigned to either a neuromuscular exercise intervention group or a control group. Both groups will be assessed before and after the 8-week intervention period.
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

January 1, 2026

First Posted

May 19, 2026

Study Start

May 1, 2026

Primary Completion (Estimated)

September 1, 2026

Study Completion (Estimated)

September 1, 2026

Last Updated

May 19, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Individual participant data (IPD) will not be shared because the dataset includes identifiable physiological and biomechanical data collected from human participants. Data sharing is restricted by ethical approval and participant consent regulations. Only aggregated results will be reported in publications.

Locations